About Us
Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
About the Job:
We are actively hiring a Research Assistant to support our Jacksonville, FL site.
Shift: Monday-Friday regular business hours
Location: Onsite
FLSA Classification: Non-Exempt
Compensation: $18.00 to $24.00 per hour (based on experience)
Essential Job Functions:
Support CRCs and site staff with protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.Document assessments and study data per regs/GCPObtain and document informed consent following federal regulations and IRB guidelinesSupport patient recruitment efforts and scheduling to meet enrollment goalsMaintain accurate source documentation and complete case report forms (CRFs)Report adverse events to supervisors or investigators as neededHelp manage study supplies, lab kits, and other trial materialsMaintain confidentiality and follow all applicable compliance and ethical standardsCommunicate effectively with research team members and document relevant study communicationsRepresent Flourish Research professionally in all interactionsPerform additional duties as assigned by management
Physical Requirements And/or Environmental Factors:
Requirements
Bachelor's degree preferred, but not requiredClinical research experience is required, and oncology clinical research experience is preferredMinimum of two years of clinical research experienceClinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injectionsFamiliar with e-source reporting via an electronic platformA clear understanding of ICH, FDA, and GCP regulationsImpeccable organizational skills and attention to detailExcellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sourcesAn ethical compass that compels the candidate to be honest, detail-oriented, and self-drivenHigh-level critical thinking skillsWorking knowledge of medical terminology and lab collection/processing/storage proceduresProficiency with computers and Microsoft Office Suite.Benefits
Flourish Research offers an excellent comprehensive benefits package to include:
Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Read LessFlourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
We are actively hiring Clinical Research Coordinators at our site in San Antonio! Clearly defined career development pathway into CRC II, Sr CRC, and even Team Lead opportunities.
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction.
Shift: Monday-Friday, 8 AM - 5:30 PM
Compensation: $24-$26/hr
RESPONSIBILITIES
Requirements
Bachelor's degree preferred, but not requiredPhlebotomy experience is required; EKG or other patient labs/processes preferredPreferably 1+ year of experience as a Clinical Research CoordinatorFamiliar with e-source reporting via an electronic platformA clear understanding of ICH, FDA, and GCP regulationsImpeccable organizational skills and attention to detailExcellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sourcesAn ethical compass that compels the candidate to be honest, detail-oriented, and self-drivenHigh-level critical thinking skillsWorking knowledge of medical terminology and lab collection/processing/storage proceduresProficiency with computers and Microsoft Office SuiteFlourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!
Benefits
Health, dental, and vision insurance plans, 401k with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays.
Flourish Research is where clinical trials thrive.
Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines.
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality.
Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
About Us:
Flourish Research represents is of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines.
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
We are actively hiring a Regional Regulatory Specialist at the Flourish Research site in Northridge, CA!
The Regulatory Specialist is responsible for managing and coordinating regulatory documents and activities for clinical research studies conducted at Flourish Research. This role involves working with site leadership, principal investigators, and regulatory bodies to ensure compliance with Flourish Research's standards, federal regulations, and sponsor protocols.
Shift: Monday - Friday, 8 AM - 5 PM
Location: 18433 Roscoe Blvd #208, Northridge, CA 91325
Compensation: $25-$26/hour for entry-level candidates, with potential flexibility for candidates with directly relevant clinical research, regulatory, healthcare administration, or other highly applicable experience.
RESPONSIBILITIES
Requirements
High school diploma or equivalent required; college degree preferred0–3+ years of experience in clinical or biological researchProficient in Microsoft Office (Outlook, Word, Excel) and platforms such as CTMS, eRegs/eDocsHighly detail-oriented, organized, and self-motivatedAble to work independently and collaboratively in a fast-paced environmentStrong written and verbal communication skillsEthical and professional in interactions with patients, sponsors, IRBs, and staffStrong critical thinking and problem-solving abilitiesDemonstrates a high level of professionalism and work ethicFlexible and willing to take on additional tasks as neededEffective at cross-departmental collaboration and issue resolutionContributes to departmental initiatives and process improvementsAssists in training new team membersMeets or exceeds 80% of annual goalsExcellent computer skills, including proficiency with Office365Benefits
Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!
Benefits: Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
About Us
Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
About the Job:
We are actively hiring a Research Assistant to support our St. Augustine, FL site.
Shift: Monday-Friday regular business hours
Location: Onsite
FLSA Classification: Non-Exempt
Compensation: $21 to $25 per hour
Essential Job Functions:
Support CRCs and site staff with protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.Document assessments and study data per regs/GCPObtain and document informed consent following federal regulations and IRB guidelinesSupport patient recruitment efforts and scheduling to meet enrollment goalsMaintain accurate source documentation and complete case report forms (CRFs)Report adverse events to supervisors or investigators as neededHelp manage study supplies, lab kits, and other trial materialsMaintain confidentiality and follow all applicable compliance and ethical standardsCommunicate effectively with research team members and document relevant study communicationsRepresent Flourish Research professionally in all interactionsPerform additional duties as assigned by management
Physical Requirements And/or Environmental Factors:
Requirements
Bachelor's degree preferred, but not requiredClinical research experience is required, and oncology clinical research experience is preferredMinimum of two years of clinical research experienceClinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injectionsFamiliar with e-source reporting via an electronic platformA clear understanding of ICH, FDA, and GCP regulationsImpeccable organizational skills and attention to detailExcellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sourcesAn ethical compass that compels the candidate to be honest, detail-oriented, and self-drivenHigh-level critical thinking skillsWorking knowledge of medical terminology and lab collection/processing/storage proceduresProficiency with computers and Microsoft Office Suite.Benefits
Flourish Research offers an excellent comprehensive benefits package to include:
Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Read LessAbout Us
Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
About the Job:
We are actively hiring a Clinical Research Coordinator to support our Philadelphia site.
Shift: Monday-Friday normal work hours
Location: Onsite Pllymouth Meeting, PA
FLSA Classification: Non-Exempt
Compensation: $25 to $36 per hour
ESSENTIAL JOB FUNCTIONS:
Execute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs.Obtain informed consent per federal regs, GCP, and IRB requirements.Ethically recruit qualified subjects to meet enrollment timelines.Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies.Schedule and conduct visits per protocol timelines.Protect confidentiality per HIPAA and all confidentiality agreements.Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor.Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy.Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies.Represent Flourish professionally in all interactions.Additional duties as assigned by management.Requirements
Bachelor's degree preferred, but not requiredMust have oncology clinical research experienceMinimum of two years of clinical research experienceClinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injectionsFamiliar with e-source reporting via an electronic platformA clear understanding of ICH, FDA, and GCP regulationsImpeccable organizational skills and attention to detailExcellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sourcesAn ethical compass that compels the candidate to be honest, detail-oriented, and self-drivenHigh-level critical thinking skillsWorking knowledge of medical terminology and lab collection/processing/storage proceduresProficiency with computers and Microsoft Office SuiteFlourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!
Benefits
Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Read LessValkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading Oncology multi-site clinical research network with expertise in Oncology research. VCT approaches clinical research with a deep sense of humanity, compassion, and sincere kindness. VCT was founded by leading Clinical Oncologist, Dr. David Berz, and has multiple sites spanning California in Century City, Panaroma City, and Murrieta, and has recently expanded to Denver, Colorado.
Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
We are actively hiring a Sub-Investigator to support our Valkyrie Clinical Trials Denver, Colorado site.
LOCATION: Onsite
FLSA: Exempt
HOURS: Monday to Friday, Day Shift, 40 hours per week
COMPENSATION: $130,000 to $150,000 per year (depending on experience)
ESSENTIAL JOB FUNCTIONS:
Represent Flourish Research in a professional and courteous manner (verbal, written, and in appearance) during all interactions with sponsors, physicians, physicians' office personnel, participants, Flourish Research employees, contract personnel, as well as any other person(s) when carrying out tasks and responsibilities. Ensure the maintenance of confidentiality of participant information by team members as appropriate and as bound by Confidentiality Agreements with Flourish Research, between Flourish Research and sponsors/CROs, and between Flourish Research and other entities while abiding by HIPAA regulations. Assume overall responsibility for the success of Flourish Research under the direction of, as applicable, the CEO, General Manager, Site Director, and Medical Director. Possess a thorough knowledge and understanding of the requirements of each study protocol. Determine whether inclusion/exclusion criteria are applicable to the study population. Follow each study's randomization procedures. Maintain protocol compliance, including implementing only protocol deviations or changes approved by the sponsor/CRO and IRB (except to eliminate immediate hazards to the participant). Review the inclusion/exclusion criteria, procedures, scheduled visits, end point criteria, and investigational product use with the research team. Ensure that a qualified physician is responsible for all trial-related medical decisions. Assess participant compliance with protocol requirements and follow-up visits. Assess participant response to therapy. Evaluate adverse experiences and determine severity and relationship to the investigational product. Ensure that medical care is provided to a participant for any adverse event(s). Document and report all serious adverse events immediately, and within 24hrs of becoming aware of the event to the sponsor/CRO and IRB. Obtain signed and dated informed consent from the study participant or participant's legal representative prior to initiating any study-related procedures. Inform the participant or legal representative about all aspects of the clinical trial. Document that informed consent has been obtained from the participant or legal representative. Always consider participant safety and welfare the priority. Ensure the accuracy, completeness, legibility, and timeliness of case report forms (CRFs). Explain any discrepancies between source documents and case report forms (CRFs). Endorse changes or corrections to a case report form (CRF). Review and sign data management queries and case report forms (CRFs) in a timely manner. Document deviations from the approved protocol. Document and explain premature unblinding of the investigational product(s). Conduct, when necessary, clinical interviews and administer a variety of psychological tests, clinical rating scales, and/or diagnostic assessments. Evaluate results through scoring and documented findings in participants’ medical records and Flourish Research CTMS, eDocs, Source/EMR. Ensure validity and reliability when administering tests/scales/assessments by complying with established standards for administering all testing and per sponsors’ protocols. Ascertain and document the reason for a participant’s premature study withdrawal. Comply with written procedures to document changes to data and/or case report forms (CRFs). Read the current investigator’s brochure, product insert, or other source information. Develop thorough knowledge and familiarity with the use of the investigational product(s). Collaborate closely with pharmacy, nursing, administration, and all study personnel to ensure excellence in study conduct and patient care. Attend Investigator meetings, SIVs, monitoring visits, and industry conferences as needed. Perform other administration duties as needed or directed by, as appropriate, the General Manager, Site Director, or Medical Director.Requirements
PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:
Work is normally performed in a typical interior clinical/office work environment. Exposure to human bodily fluids; Laboratory procedures to obtain specimens and processing of specimens; Participant/Patient Care; Daily computer use; Local travel required to ensure coverage at all sites, if multiple local locations; Occasional travel for meetings and conferences; Ability to properly lift thirty-five pounds and occasionally more than thirty-five pounds.MINIMUM REQUIREMENTS:
Education: Medical (M.D.) degree, Doctor of Osteopathy (D.O.), Doctor of Nursing Practice (D.N.P.), Physician’s Assistant (P.A.), Advanced Practice Nurse Practitioner (APRN), Doctor of Psychology (PsyD).
Experience: A minimum of 2 years’ experience in performing physicals, assessing, and treating patients. 1-3+ years' experience within the field of oncology clinical research; early phase oncology clinical trial experience preferred.
Knowledge and Skills:
Strong supervision, interpersonal, and communication skills. Able to make good, sound decisions under stressful situations and time constraints. Must be able to make sound medical judgments on the health and safety of subjects during their participation in a clinical research study. Maintain professional and technical knowledge by attending educational workshops in other activities to maintain continuing medical education requirements. Review professional publications. Must possess exceptional organizational and planning skills and good documentation skills. Must have good conflict resolution skills and be committed to quality and honesty. In-depth knowledge of the clinical research process, including Good Clinical Practices.Benefits
Flourish Research offers an excellent comprehensive benefits package to include: Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
This is an excellent opportunity for those with clinical experience who want to enter the clinical research industry!
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
We are actively hiring Clinical Research Coordinator Assistants at our Clinical Trials of Texas site in San Antonio!
The Clinical Research Coordinator Assistant is critical in supporting the Clinical Research Coordinators and the research team in providing an impeccable patient experience in every interaction. Your role will include a variety of tasks, from patient recruitment, source documentation, data entry, and direct patient interaction during site visits.
Shift: Monday-Friday, 8:30 AM - 5 PM
Location: 5430 Fredericksburg Rd., Suite 200, San Antonio, TX 78229
RESPONSIBILITIES
Requirements
Bachelor's degree preferred but not requiredMust have either clinical research experience OR clinical skills, such as taking vitals, phlebotomy, EKGs, etcImpeccable organizational skills, attention to detail, and people skills, as you will be interacting directly with patientsExcellent communication and interpersonal skills to effectively interact with the Principal Investigator, CRCs, other members of the research team, Study Sponsor/CROs, potential subjects, and referral sourcesAn ethical compass that compels the candidate to be honest, detail-oriented, and self-drivenHigh-level critical thinking skillsWorking knowledge of medical terminology and lab collection/processing/storage proceduresProficiency with computers and Microsoft Office SuiteFlourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!
Benefits
Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 company holidays.
Flourish Research is where clinical trials thrive.
Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, oncology and vaccines.
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
We are actively seeking a Sub-Investigator Nurse Practitioner for our Leesburg, Florida site.
Shift: Monday-Friday, normal business hours
Location: Onsite
FLSA Classification: Exempt
Compensation: $125,000 - $140,000 annual salary (depending on experience)
Responsibilities
A. Represent Flourish Research in a professional and courteous manner (verbal, written, and in appearance) during all interactions with sponsors, physicians, physicians' office personnel, participants, Flourish Research employees, Flourish Research contract personnel, as well as any other person(s) when carrying out tasks and responsibilities.
B. Ensure the maintenance of confidentiality of participant information by team members as appropriate and as bound by Confidentiality Agreements with Flourish Research, between Flourish Research and sponsors/CROs, and between Flourish Research and other entities while abiding by HIPAA regulations.
C. Possess a thorough knowledge and understanding of the requirements of each study protocol including any amendment changes, as applicable.
D. Work closely under the Primary Investigator to manage the safety of study participants, assess inclusionary and exclusionary study criteria, monitor laboratory results, ensure appropriate follow up as necessary, and maintain adherence to study protocol and procedures.
E. Perform study-related procedures, injections, physical examinations, clinical interviews, clinical rating scales, psychological testing, and neurological assessments. Interpret laboratory results, facilitate participant care, and ensure appropriate follow up per protocol.
F. Maintain protocol compliance, including following schedule of assessments, implementing only protocol deviations or changes approved by the sponsor/CRO and IRB (except to eliminate immediate hazards to the participant).
G. Acquire thorough knowledge of the inclusion/exclusion criteria, procedures, scheduled visits, end point criteria, and investigational article use and share relevant information with the research team to include information in the current investigator’s brochure, product insert, or other source information, as well as other information about the investigational product(s).
H. Assess participant compliance to investigational product. Evaluate adverse experiences and determine severity and relationship to the investigational product.
I. Ensure that medical care is provided to a participant for any adverse event(s) as needed.
J. Document and report all serious adverse events to the sponsor/CRO and IRB within 24 hours of the site’s knowledge of the event.
K. Obtain signed and dated informed consent from the study participant or participant's legal representative prior to initiating any study-related procedures.
L. Inform the participant or legal representative about all aspects of the clinical trial.
M. Document that informed consent has been obtained from the participant or legal representative.
N. Always consider participant safety and welfare the priority.
O. Ensure the accuracy, completeness, legibility, and timeliness of source documentation and case report forms (CRFs) as applicable.
P. Review and sign data management queries and case report forms (CRFs) in a timely manner as applicable.
Q. Document and explain premature unblinding of the investigational product(s) when necessary.
R. Evaluate results and documented findings in participants’ medical records and Flourish Research CTMS, eDocs, Source.
S. Ensure validity and reliability when administering tests/scales/assessments by complying with established standards for administering psychometric testing and per sponsors’ protocols.
T. Ascertain the reason for a participant’s premature study withdrawal.
Requirements
PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:
A. Work is normally performed in a typical interior clinical/office work environment.
B. Participant Care
MINIMUM REQUIREMENTS:
Education: Medical (M.D.) degree, Doctor of Osteopathy (D.O.), Doctor of Nursing Practice (D.N.P.), Advanced Practice Registered Nurse (A.P.R.N.), Physician’s Assistant (P.A.), Doctor of Psychology (PsyD).
Experience: A minimum of 2 years’ experience in performing physicals, assessing, and treating patients. 1-3+ years' experience within the field of clinical research or biological research preferred; however, is not required.
Knowledge and Skills:
A. Possess strong supervision, interpersonal and communication skills.
B. Be able to make good, sound decisions under stress and time constraints.
C. Be able to make sound medical judgments on the health and safety of subjects during their participation in a clinical research study.
D. Maintain professional and technical knowledge by attending educational workshops in other activities to maintain continuing medical education requirements.
E. Review professional publications.
Possess exceptional organizational and planning skills and good documentation skills.
F. Have good conflict resolution skills and be committed to quality and honesty.
G. Possess in-depth knowledge of the clinical research process, including Good Clinical Practices.
Benefits
Flourish Research offers an excellent comprehensive benefits package to include:
Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Read LessAbout Us
Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
About the Job:
We are actively hiring a Research Assistant to support our North Miami, Florida site.
Shift: Monday-Friday regular business hours
Location: Onsite
FLSA Classification: Non-Exempt
Compensation: $21 to $23 per hour
Essential Job Functions:
Physical Requirements And/or Environmental Factors:
Requirements
Bachelor's degree preferred, but not requiredClinical research experience is required, and oncology clinical research experience is preferredMinimum of two years of clinical research experienceClinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injectionsFamiliar with e-source reporting via an electronic platformA clear understanding of ICH, FDA, and GCP regulationsImpeccable organizational skills and attention to detailExcellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sourcesAn ethical compass that compels the candidate to be honest, detail-oriented, and self-drivenHigh-level critical thinking skillsWorking knowledge of medical terminology and lab collection/processing/storage proceduresProficiency with computers and Microsoft Office Suite.Benefits
Flourish Research offers an excellent comprehensive benefits package to include:
Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
Read LessValkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading Oncology multi-site clinical research network with expertise in Oncology research. VCT approaches clinical research with a deep sense of humanity, compassion, and sincere kindness. VCT was founded by leading Clinical Oncologist, Dr. David Berz, and has multiple sites spanning California in Century City, Panaroma City, and Murrieta, and has recently expanded to Denver, Colorado.
Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
We are actively hiring a Senior Clinical Research Coordinator to support our Valkyrie Clinical Trials Denver, Colorado site.
LOCATION: Onsite
FLSA: Non-Exempt
HOURS: Monday to Friday, Day Shift, 40 hours per week
COMPENSATION: $34-$39 per hour (depending on experience)
Requirements
ESSENTIAL JOB FUNCTIONS:
Read, understand, and ensure the completion of all protocol required patient visits and procedures Clearly and concisely document patient assessments, treatments, observations, test results and other study related information per federal regulations, protocol requirements and GCP Guidelines. Obtain patient informed consent, and reconsent as required, according to federal regulations, GCP and IRB requirements while educating patients on study requirements, timelines, and visit expectations. As Senior CRC, lead and mentor other research staff and serve as an escalation point and SME. Is diligent in enrolling qualified study participants into appropriate protocols within the sponsor’s timeline while following regulations and rules governing medical ethics, IRB, GCP and ICH guidelines. Complete all required training in a timely manner. Schedule and conduct patient visits according to protocol requirements and timelines. Maintain written source documentation of patient visits and protocol related activities per ALCOA guidelines Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets and respond to queries generated by the sponsor in a timely manner Maintain confidentiality of all patient and protocol activities and information as appropriate and as bound by Confidentiality Agreements with Valkyrie/Flourish Research, between Valkyrie/Flourish and sponsors, and between Valkyrie/Flourish and other entities, as well as HIPAA regulations. Promptly document and report adverse events to supervisor and/or Principal Investigator/Sub-Investigator as deemed necessary. Report Serious Adverse Events (SAEs) to sponsor within 24 hours of becoming aware of the SAE. Also report the SAE to the supervisor, Principal Investigator and/or Sub-Investigator immediately. Account for clinical trial materials (i.e., CRFs, study drug, lab supplies, and/or other required items) and ensure availability of appropriate amounts for the conduct of the study. Maintain ongoing communication with Team Lead I; Team Manager/Research Manager; Principal Investigator; Sub-Investigators and other people assisting with the trial and documenting these communications according to protocol requirements and Valkyriepolicies. Attend required training courses/conferences in order to stay abreast of current and changing federal regulations and Valkyrie policies. Pursue educational opportunities to increase knowledge of the research process and associated rules and regulations governing clinical research. Attend Investigator Meetings, SIVs, team meetings, and/or other trainings as directed. Perform all study-related duties in a time- and cost-effective manner in adherence with Valkyrie, policies. Represent Valkyrie, Clinical Trials in a professional and courteous manner (verbal, written and in appearance) when interacting with Valkyrie staff, sponsors, IRBs, patients/participants, nursing and medical staff members of various clinics, hospitals, and physician’s offices. Additional duties as assigned by management.PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS:
Work is normally performed in a typical interior/office work environment.Travel required but minimal.Exposure to human bodily fluids. Laboratory processing procedures.Participant care.Daily computer use.Occasional night and weekend work schedules.The ability to properly lift thirty-five pounds and occasionally more than thirty-five pounds.The ability to drive, and daily availability of an automobile.
MINIMUM REQUIREMENTS:
Experience:
Education: Bachelor's degree preferred; however, is not required. Clinical research certification is a plus Experience: A minimum of 3 years’ experience as an oncology CRC, with at least 1 year of experience in early phase oncology research preferred.
Knowledge and Skills:
Benefits
Flourish Research offers an excellent comprehensive benefits package to include: Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, employee referral program, employee assistance program, life insurance, disability insurance, and a generous PTO plan covering vacation, sick, personal days and 8 paid holidays.
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
