Research Associate
About The Position
The Cancer Clinical Trials CRC I supports the research team in conducting clinical trials in accordance with Good Clinical Practice under direct supervision. Mentored by an experienced Clinical Research Coordinator II or Senior Clinical Research Coordinator, this position is responsible for primary collection and management of patient clinical information related to clinical-trial participation. The role ensures timely collection and shipment of protocol-related samples. It obtains informed consent for non-interventional studies and supports investigators during the informed-consent process for interventional trials. The Research Associate collects, maintains, organizes, compiles, registers, and submits study information as required by sponsors. Clinic attendance may be needed for research activities such as recruitment support and questionnaire administration.
Requirements
- Bachelor's degree required.
Nice To Haves
- Master's degree preferred.
- ACRP or SOCRA certification preferred.
- Bachelor's degree in life science or public health preferred.
- Medical degree or foreign equivalent preferred.
Responsibilities
- Collect and record study data and enter information into databases.
- Support clinical research activities, including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agencies, and administering lifestyle questionnaires.
- Maintain source documents and subject files in accordance with hospital procedures.
- Review charts to ensure accurate and complete compilation of subject data.
- Under direct supervision and as assigned, coordinate SFV and SIV activities and monitor scheduling, including remote-access setup, for multiple studies.
- Secure, deliver, and ship clinical specimens as required by study protocols.
- Ensure timely collection and shipment of protocol-related samples.
- Obtain informed consent for non-interventional studies and support investigators in the informed-consent process for interventional trials.
- Collect, maintain, organize, compile, register, and submit study information as required by sponsors.
- Attend clinic as needed to support recruitment activities and administer questionnaires.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
