Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!
QPS has an immediate opening for Senior Specialist, Sample Management QC supporting our Translational Medicine Department. This role is 100% desk-based. All QC activities are performed through document review, data verification, and system‑based checks. No laboratory or hands‑on QC testing is involved. The position requires extreme attention to detail, organization, multi-tasking, and comfort interacting with people who might be junior or senior to the incumbent. The ideal candidate is someone who can share responsibilities and shift priorities when necessary to do what is needed in the moment – especially in a dynamic environment.
QPS's Sample Management Team ensures that client samples and other controlled materials are received, stored, distributed, tracked and returned safely, securely and without loss or damage. The process is regulated and vital to the success of clinical trials around the world. Our team is comprised of professionals from diverse backgrounds such as customer service, restaurant/retail, programming, data analysis, and various physical sciences. We work together to ensure that the biological samples received are stored, logged, tracked, distributed, and reported back to our sponsors per GLP regulations and internal & external SOP requirements.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged to achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
Create and maintain Sample Receipt notebooks from creation to archivalUse our LIMS (database) for tracking of samples through their life cycle at QPSPerform QC of Sample Receipt records against an electronic database to ensure they comply with FDA and GLP regulations, client protocol, and QPS SOPsEnsure all appropriate GLP paperwork is included with sample receipt packetEnsure shipped samples are received and reconciled per client protocol and shipping manifestEnsure any referenced client correspondence can be verifiedMonitor documentation of storage changes, disposal, return of samples as neededMaintain TLM Sample Receipt Table Request log and communicate any timeline issues internally to Principal InvestigatorCompile and/or perform QC on Sample Receipt tables prior to submission to QAQC QPS generated manifestQC various Data Management generated reports prior to submitting to Principal InvestigatorAssist SMT with general documentation questionsReconcile shipment packets against TLM DashboardCommunicate any new SOP revisions to the team and reconcile Employee Qualification Manuals annuallyUnderstand and abide by HIPPA & GDPR compliant privacy measuresWork Location
This job will be 100% QPS-office/facility basedRequirements
Combination of relevant education and experience that provides sufficient knowledge and skills to ensure incumbent's success in this role, such as:University/college degree in a relevant scientific discipline and/orDemonstrated experience in CRO, Clinical Research or another relevant fieldExperience in an FDA-related or other regulated industry laboratory is preferredOrganized, with good detail-orientationProficiency with MS Office, including ExcelGood interpersonal skillsWhy You Should Apply
Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.Structured Career Ladders that provide excellent growth based on your personal aspirations.Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability InsurancePark-like setting in Newark, DelawareInternal committees designed with the needs and enjoyment of QPS employees in mind.QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
Read LessDo you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! Mass Spec Services (MSS) ensures that all the mass spectrometers (55+ QqQ and Q-TOF), LC, SFC, and other related bioanalytical instruments are in good working order. The process is vital to the operational success of GBA and of preclinical, nonclinical, and clinical trials around the world. In this role, MSS personnel will maintain, troubleshoot, repair, help with installation, and perform IQ/OQ/PQ of bioanalytical equipment with minimum supervision, maintain a clean/safe lab, and ensure the smooth operation of the facility.
The GBA department’s expertise lies in the quantitation of small molecules, oligonucleotides, peptides, proteins, and biomarkers using various mass spec techniques. We have been pivotal in supporting most of the HIV/HBV/HCV, multiple ADCs, and 9 of the last 16 oligonucleotides therapeutics approved by FDA and EMA.
No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
Understand, evaluate, troubleshoot, and repair LC-MS/MS (QqQ) systems, LCs, and other associated bioanalytical equipment problems.Perform planned preventive maintenance, calibration, and maintenance of the LC-MS/MS, LC, and other associated bioanalytical equipment.Perform software (IQ/OQ/PQ) validations on all new equipment.Maintain inventory of spare parts for MS and LC systems.Requirements
Advance degree in LC-MS (Ph.D.) or M.S. plus ≥4 years or B.S. plus ≥10 years in relevant industry experienceHands-on experience in triple quadrupoles requiredExperience with UHPLC equipment required; Experience with Shimadzu UHPLC is a plus; Experience with SFC is a plusA background or education in Analytical Chemistry, Biochemistry, Pharmaceutical Chemistry, Pharmacology, Microbiology is considered added value.Work Location
This job will be 100% QPS-office/facility basedWhy You Should Apply
Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.Structured Career Ladders that provide excellent growth based on your personal aspirations.Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability InsurancePark-like setting in Newark, DelawareInternal committees designed with the needs and enjoyment of QPS employees in mind.QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
Read LessDo you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As a Part-time Housekeeper, you will be responsible for executing the daily duties required to establish and maintain a safe, hygienic, and aesthetically pleasing environment.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II – IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
Provide routine cleaning service to assigned areas by following established procedures and schedules.Meets all scheduling requirements and direction from supervisors to complete routine housekeeping services.Dust and wet mopping of floors, vacuuming, dusting, and damp wiping of surfaces, wall washing, trash collection and removal, cleaning of restrooms and patient areas, non-clinical areas, and all other assigned duties.Maintain an inventory of cleaning and toiletry supplies. Other tasks as requested by supervisor.Requirements
Minimum a high school diploma or GEDBilingual English and Spanish is preferred.Good communication skillsKnowledge of various cleaning products and when to use themAbility to clean and disinfect various surfacesAbility to lift and move at least 50 poundsGood organization skillsKnowledge of safety guidelines when working with chemical cleanersExcellent time-management skillsDemonstrate that is a team playerMust be flexible to work evenings, weekends, and holidays as needed.Why You Should Apply
Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performanceQPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Stage Clinical and Phase I IV Clinical Research services.
We welcome individuals who want to be part of our growing organization. QPS is an innovative, dynamic organization that strives to employ talented, caring and committed employees who will work collaboratively towards achieving our mission of improving human health and the quality of life. QPS offers challenging and rewarding work in its four core business areas and support functions. Underpinning the operation is a culture that values diversity, innovation and accountability. Employees are encouraged to take responsibility and achieve their best, both as individuals and as team members.
The Clinical Pharmacist works closely with Principal Investigators and Clinical Operations leadership to support the safe and compliant conduct of clinical research studies. This role is responsible for the receipt, storage, preparation, dispensing, documentation, and accountability of investigational products used in clinical trials.
The Clinical Pharmacist ensures compliance with study protocols, FDA regulations, ICH/GCP guidelines, USP standards, and applicable state and local requirements. This position also supports pharmacy operations through inventory management, study drug tracking, documentation, and subject safety monitoring.
What you will doReceive, inspect, document, and maintain accountability for investigational products.Prepare, dispense, and reconcile study medications according to protocol requirements and applicable regulations.Maintain accurate records of study drug inventory, storage conditions, temperature monitoring, and accountability logs.Manage investigational product inventory, including retention and storage of study medications from completed studies as required.Support occasional compounding activities in accordance with protocol requirements and applicable USP standards.Follow study-specific randomization procedures and ensure proper dispensing of investigational products.Monitor, document, and communicate adverse events and medication-related concerns to the Principal Investigator and study team.Participate in protocol training and provide pharmacy-related training to research staff as needed.Assist with SOP maintenance and ensure pharmacy operations remain inspection-ready.Support sponsor visits, monitoring visits, audits, and regulatory inspections.Collaborate with clinical operations, investigators, sponsors, and other study personnel to support successful study execution.Report protocol deviations, compliance concerns, or pharmacy-related issues promptly to Clinical Operations leadership and the Principal Investigator.Execute clinical trials in compliance with study protocols, Good Clinical Practice (GCP), FDA regulations, QA/QC procedures, OSHA guidelines, and applicable state and local regulations.What we seekActive State Registered Pharmacist license required.Clinical research experience preferred.Experience in a hospital, clinical, or research pharmacy environment preferred.Knowledge of FDA, ICH, GCP, and applicable pharmacy regulations.Strong attention to detail and documentation practices.Excellent communication and organizational skills.Ability to work effectively in a collaborative clinical research environment.Flexibility to support occasional weekend, holiday, or on-call study activities as needed.Why QPS?At QPS, you will have the opportunity to contribute directly to clinical research that helps bring new therapies to patients. We offer a collaborative work environment, meaningful career opportunities, and the chance to work alongside experienced clinical research professionals dedicated to advancing human health.
Location: Missouri (On-site)
EEO Minorities/Females/Protected Veterans/Disabled
QPS is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. QPS prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. QPS conforms to the spirit as well as to the letter of all applicable laws and regulations.
#LI-DNI
Read LessDo you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! As a Facilities Support Associate, you will be responsible for maintaining a clean, sanitary, safe, and orderly environment throughout the facility. This role performs routine cleaning, housekeeping, and maintenance support tasks to ensure all assigned areas meet cleanliness and safety standards.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of services, including Early Phase Clinical and Phase II – IV Clinical Research services. The QPS location in Miami, Florida is a multi-specialty research center employing clinical research professionals, including board-certified physicians, in a 32,000 square foot space. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
Clean all areas under the inpatient/outpatient suites including all restrooms, patient areas, offices, nurses’ stations and laboratory.Operate cleaning equipment like auto floor scrubbers and restock cleaning supplies as needed.Responsible for maintaining linen and other miscellaneous supplies and empty all trash.Check to replace toilet paper, paper towels and hand soap as needed. Before leaving, they review their list of priorities to make sure they completed all their tasks.Respond to and resolve minor facility issues, including unclogging toilets and drains when appropriate.Replace light bulbs and perform other basic maintenance tasks as assigned.Move and rearrange furniture, equipment, and supplies as needed for operational or event requirements.Help maintain the overall appearance, cleanliness, and functionality of the facility.Identify and report maintenance concerns, safety hazards, or repair needs to management in a timely manner.Other tasks as requested by the supervisor.Requirements
Minimum a high school diploma or GEDGood communication skillsKnowledge of various cleaning products and when to use themAbility to clean and disinfect various surfacesAbility to lift and move at least 50 poundsGood organization skillsKnowledge of safety guidelines when working with chemical cleanersExcellent time-management skillsDemonstrate that is a team playerMust be flexible to work evenings, weekends, and holidays as needed.Why You Should Apply
Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability InsuranceQPS is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
The Senior Specialist, Lab Trainer is a junior member of the Training (TRN) support unit within the Department of Translational Medicine (TLM) and is responsible for all daily activities that support the smooth operation and regulatory compliance of TLM. This is a non-production, oversight role.
The Senior Specialist Lab Trainer is an individual who assists in the training of staff on items including but not limited to technical aspects of the laboratory and associated analytical practices. These functions are guided by the principles of Good Clinical Practices (GCPs), Good Documentation Practices (GDPs), and Good Laboratory Practices (GLPs) (21 CFR Parts 11, 50, 56, 58) as well as related guidance from the Organization for Economic Co-operation and Development (OECD), European Medicines Agency (EMA) and (Clinical Laboratory Improvement Amendments (CLIA) as appropriate. Detailed responsibilities include, but are not limited to, support of these objectives:
Staff are skilled, trained and available to support new business.Staff are developed and trained in an ongoing manner.The facility, devices and material under their control is safe, proper, secure, correctly documented, cleaned, inspected, maintained, calibrated, validated and sufficient for their assigned tasks.Computer systems are suitable for their intended purpose and are validated and maintained.Materials and records are retained, archived and maintained under conditions that ensure their integrity and continued access.The Senior Specialist, Lab Trainer spends a majority of their time on the Laboratory floor as a mentor, technical guide and process monitor. Among the expected roles are aiding senior training staff in the following:
Onboarding new hires with technical laboratory training with regards to ligand binding assays and other areas as appropriate.Re-train existing staff to improve their laboratory techniques as requested.Development and training of junior staff both technically and in the soft skills needed for advancement in a fast-paced CRO environment.Essential Functions
Real- Time Staff StewardshipMaintain TLM-DE operational capacity by orienting, on-boarding and training new staff.Organize, author and administer recurring staff training in compliance with corporate SOPs.Coordinate with leadership on issues which impact laboratory services.Real-Time Laboratory StewardshipHelp to, and direct lab staff in best habits to keep the laboratories and all the devices clean, operational and presentable.Interact with support teams for maintenance and qualification issues.Provide input to management on future needs including formulating and executing strategies, renovations, and infrastructure for adequate manning, space, and facilities.Maintain laboratory equipment performance by developing and executing operations, quality, and troubleshooting procedures.Govern safety checks of laboratories, including biohazards.Maintain inventory of reagents and consumables; anticipate supply needs; place and expedite orders for supplies; verify receipt of supplies.CommunicationRespond to every communication, internal and external, in real-time.If this is not possible, respond within a few hours, preferably before close of business (COB) for that day.If the response requires examination or coordination with others, immediately reply as such, and set a time to provide a resolution, preferably within a business day.Immediately update superiors and/or internal stakeholders regarding lapses in timelines, assay performance, data, or reports and work with them to effectively address any issues that may arise.Assist in communicating issues to stakeholders clearly and completely and list potential solutions.Work Location
This job will be 100% QPS-office/facility basedRequirements
Education / Experience
Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as: University/College Degree in relevant Scientific discipline, and/or Demonstrated experience in CRO, Clinical Research, or other relevant field. Experience in a Regulated industry laboratory preferred.Why You Should Apply
Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.Structured Career Ladders that provide excellent growth based on your personal aspirations.Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability InsurancePark-like setting in Newark, DelawareInternal committees designed with the needs and enjoyment of QPS employees in mind.QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! Our compliance with applicable regulatory guidelines and requirements is critical to our pharmaceutical clients. In the Quality Assurance role, you will put your scientific education, experience and on-the-job training to work by performing protocol, raw data, and report audits for compliance with regulatory requirement (GLP, GCP & Part 11), SOPs, and protocol, reporting all findings from the audits and inspections to Study Directors, Principal Investigators, Test Site Management, Test Facility Management and Operational Management and scientific personnel.
No visa sponsorship (e.g. H‑1B, L‑1, E) will be provided for this active position, now or in the future. Applicants must currently be authorized to work in the U.S. on a permanent or unrestricted basis.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
Audit scientific data for various clinical and nonclinical study records and reports to ensure proper study conduct and to ensure raw data results reflect the requirements specified in the respective protocol, SOP(s), validated method, study plan, lab manual and analytical procedure.Inspect lab work in situ to ensure compliant study procedures, facilities, equipment, personnel training, computer systems and respective raw data documentation. Audit and inspect the Quality Management System to identify any quality improvements necessary to maintain compliant quality systems.Identify areas of noncompliance and formulate recommendations for corrective and preventative actions necessary to improve quality and compliance.Issue audit reports to responsible scientists, personnel and Management for them to formally respond to Quality Assurance findings and recommendations.Verify audit report follow-up responses in order to close each audit issued.Assist with client and government audits and any department goals as directed by line management. After hours incentive work potential.Work Location
This job will be 100% QPS-office/facility basedRequirements
Bachelor’s degree in a related scientific discipline such as Biology, Biochemistry, Immunology, Analytical Chemistry preferred. Lab experience and/or experience working within GLP, GCP or GMP Quality Assurance preferred but not required.
Why You Should Apply
Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.Structured Career Ladders that provide excellent growth based on your personal aspirations.Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability InsurancePark-like setting in Newark, DelawareInternal committees designed with the needs and enjoyment of QPS employees in mind.QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
Read LessSince its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Stage Clinical and Phase I IV Clinical Research services. We welcome individuals who want to be part of our growing organization. QPS is an innovative, dynamic organization that strives to employ talented, caring and committed employees who will work collaboratively towards achieving our mission of improving human health and the quality of life. QPS offers challenging and rewarding work in its four core business areas and support functions. Underpinning the operation is a culture that values diversity, innovation and accountability. Employees are encouraged to take responsibility and achieve their best, both as individuals and as team members.
Description:
The position of Clinical Operations Specialist/Phlebotomist will be working PRN in our Clinical Operations Department performing phlebotomy, obtaining vital signs, sample collection, customer service and completing documentation. Our phlebotomists are responsible for performing venipuncture and accurate organization, recording, and processing of blood samples in accordance with SOPs/PRCs and protocol specifications. This position must be able to work with other clinical staff to ensure procedures are completed in a coordinated manner and in accordance with the processes and procedures that ensures compliance with applicable rules and regulations relative to human subjects in research.
This position's working hours are dictated by study activity and could include working hours on weekends/evenings.
Responsibilities:
Read and understand the guidelines of the study protocols. Perform venipuncture Label and QC specimen containers according to protocol specificationsMaintain ability to work effectively with other people including both participants and other members of the clinical team Record specimen collection accurately Process samples according to protocol specifications Patch assessment evaluationsQUALIFICATIONS:
Must have current high school diploma or General Education Degree (GED) or equivalent relevant work experience.1 year experience as a phlebotomistExperience performing vitals sign checks is preferredOutstanding customer service skillsComfortable working in a fast-paced environmentOutstanding customer service skillsConsistently demonstrate dependability and punctualityDisclaimer
The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed.
EEO Minorities/Females/Protected Veterans/Disabled
QPS is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. QPS prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. QPS conforms to the spirit as well as to the letter of all applicable laws and regulations.
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! If you have a Bachelor’s degree in MIS or Computer Science, or a high school diploma and demonstrated database experience, along with a desire to develop your skills, this may be the job for you. Leveraging the QuickBase platform, this staff member will develop, test, release and maintain applications in a development environment, including architecture, data integration, and the dashboard used by many of QPS’ operations groups.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
Please visit our website (www.qps.com) for more information and to see all current openings.
The Job
Manage and implement database security and user accounts.Assist with the design and development of data models.Assist with training and problem solving as needed, educating users on portals, protocols, policies, procedures, and services to enhance the overall user experience.Provide technical support on QuickBase, as well as basic QuickBase development.Define and implement application architecture including relational data structures, user interfaces, role and permission-based data access.Assist in QuickBase application development and implementation.Assist in developing QuickBase platform featuresRequirements
Bachelor’s degree in MIS, Computer Science, or related discipline preferred≥ one (1) year database experienceExperience in QuickBase preferred, but not requiredAnalytical thinkingCritical information seekingWhy You Should Apply
Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.Structured Career Ladders that provide excellent growth based on your personal aspirations.Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability InsurancePark-like setting in Newark, DelawareInternal committees designed with the needs and enjoyment of QPS employees in mind.QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
