Job Description

Clinical Research Associate - Oncology Research - Full Time

SUMMARY: Accountable for assisting investigators in screening patients for potential study enrollment, assists in the scheduling of patients for study visits as per the study protocol, creating study documents, extrapolating data and completing electronic data submissions. Prepares for and participates in monitoring and auditing activities. Responsible for processing, filing and maintaining protocol regulatory documents. Coordinates in the collection and shipment of specimens, imaging documents and other items per the study protocol. Collaborates and participates in identifying and addressing quality assurance issues and developing departmental standards. Assures compliance with the IRB (Local or CIRB) Policies, institutional policies, Good Clinical Practice and regulatory authorities inclusive of State and Federal regulations for the conduct of cancer research funded by the National Cancer Institute and other sponsors. May attend a Children's Oncology Group (COG) conference on a rotation schedule.

REQUIREMENTS: This position requires a Bachelor's Degree or equivalent experience. Certified Clinical Research Professional (CCRP) is preferred. Minimum one (1) year experience in data management, COG, and/or research is preferred. Computer literate with Microsoft Office is required. Medical office experience and/or hospital experience, medical terminology and strong written and verbal skills required.

POSITION DETAILS: Full time 80 hours per pay period, day shift.


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