Each of CenExel's research sites specializes in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well-respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have inpatient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Hourly Rate: $20.00 + 4 hours OT each shift (depending on experience, education, etc)
Schedule:
Must have open availability. 3 X 12-hour shifts.Shift (6:00 am - 6:00 pm) Must be able to work weekendsJob Summary:
Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
Creating and maintaining patient charts for all assigned studies.Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.Assisting Coordinators in assessments, including but not limited to, blood pressure, urine collection.Communicating with study participants, caregivers, third party vendors and laboratories as needed.Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.Aiding Coordinators in the facilitation of study monitoring visits.Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.Education/Experience/Skills:
California Medical Assistant Certification (Required)Interest in and knowledge of specific study indications.Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).Skilled in organization and record maintenance.Skilled in developing and maintaining effective working relationships with supervisors and co-workers.Strong personal initiative and attention to detail.Ability to react calmly and effectively in emergency situations.Ability to interpret, adapt and apply guidelines and procedures.Ability to clearly communicate both orally and verbally.Working Conditions:
Indoor, Office environment.Essential physical requirements include sitting, typing, standing, and walking.Lightly active position, occasional lifting of up to 20 pounds.Reporting to work, as scheduled, is essential.CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Read LessJob Category: Lab/Pharmacy
Requisition Number: LABTE003951
Location: Los Alamitos, CA 90740, USA
Job Details
DescriptionAbout Us:
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Hourly Range: $20.00 - $22.00/hr (Depending on education, experience, and skillset)
Schedule: 3:00 pm - 11:30 pm (Monday - Friday) + and be available to work every other weekend as part of your normal schedule
The first 2-3 weeks of training would require working an AM shift.
Essential Responsibilities and Duties:
Have full knowledge of laboratory procedures and processes per protocol, laboratory manual, shipping manual, etc.Assist the laboratory manager in site preparation for study conduct.Assist in the creation of laboratory documents (i.e. harvest logs, etc.)Assist in the preparation of collection tubes, vials, study supplies for visits.Monitor temperature of laboratory sample storage and address any excursions.Maintain harvest logs, chain of custody, laboratory sample manifest/inventory logs and/or memos.Pack and properly label all study materials for storage or return to sponsor upon study close out.Obtains samples per protocol and documents process in source documents.Processes samples according to protocol. Ensures centrifuge settings are appropriate for processing according to protocol.Performs regular inventory of supplies and orders as needed to ensure lab supplies are adequate and available for study visits.Stores samples in an upright position in appropriate shipping boxes in the freezer. Stores primary and secondary samples in separate shipping boxes.Ensures freezer/refrigerator temperature is within range for protocol and ensures appropriate logs are kept.Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.Education/Experience/Skills:
Must be able to effectively communicate verbally and in writing.Minimum: High School graduate or have GED equivalency.Blood draw experience or CPT Certification (Required)Motivated to work consistently in a fast-paced and rapidly changing environment.Working Conditions:
Indoor, Office environment.Indoor, Clinic environment.Essential physical requirements include sitting, typing, standing, and walking.Lightly active position, occasional lifting of up to 20 pounds.Reporting to work, as scheduled, is essential.CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
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