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Astera Cancer Care · 1 day ago

Clinical Research Coordinator

East Brunswick, NJ

Full-time

Onsite

Entry Level

1+ years exp

Astera Cancer Care is dedicated to providing excellence in patient care and research within the communities of New Jersey and Pennsylvania. As an Oncology Clinical Research Coordinator, you will manage clinical trial activities, recruit participants, and ensure compliance with regulatory standards for successful study management.

Clinical TrialsHealth CareHealth DiagnosticsHospitalOncology

Responsibilities

Provide overall coordination of study-related activities for patients enrolled in cancer research studies through the Astera research program

Coordinate with Principal Investigators, Supervisor and study sponsors and CROs to ensure that clinical research activities are performed in accordance with local and federal regulations and adhere to policies and procedures of Astera and the sponsors and CROs

Assist in the coordination of tests and visits for patients and collaborate with the Astera study team to maximize work efficiency and productivity

Assist in IRB submissions and interact with the Supervisor to maintain regulatory documents and administrative files for each protocol

Work with research nurses, treating physicians, and Principal Investigators to confirm that each patient meets eligibility criteria specified for protocols and enrollment into clinical trials

Maintain patient and regulatory research records

Confer with all members of the clinical team to confirm appropriateness and timeliness of tests

Collect follow-up data on patient’s post-treatment as required by the protocol

Submit weekly reports to Supervisor, tracking patient screening/enrollment and subject status

Enter research data into a centralized database as per protocol requirements

Attend investigator meetings as required or requested by the Principal Investigator

Prepare other study materials as requested by the Principal Investigator such as informed consent documents, case report forms, enrollment logs and drug/device accountability logs

If applicable, able to prepare blinded and unblinded study drugs

If applicable, act as primary coordinators for unblinded team

Qualification

Clinical research experienceOncology experiencePharmacy Technician certificationEDCIWRS experiencePatient recruitment skillsMicrosoft applicationsCommunicationTime management skills