We intend to achieve our objectives through our team of highly skilled, accomplished professionals who share a determination to meaningfully improve the diagnosis and treatment of patients with prostate cancer. If you thrive in an entrepreneurial, stimulating environment where initiative and individual contributions are valued and rewarded, we would like to hear from you.
Note to Recruiters
Third party recruiters and search agencies are important to staffing efforts at Progenics, and we value our partnerships. All staffing vendors must have a written agreement in place in order to receive compensation for any candidate referrals. Progenics does not accept unsolicited resumes from third party agencies for open positions.
If you have questions about our recruiting policies or practices, please contact the Progenics HR team. Progenics is an Equal Opportunity/Affirmative Action Employer M/F/D/V.
The Lead Clinical Research Associate (LCRA) is responsible for the performance of assigned Field Based Clinical Research Associates (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and federal regulations. The LCRA acts as a primary liaison between Field Based CRAs and the Clinical Trial Manager (CTM).
The Clinical Project Manager (CPM) assists in the planning and execution of clinical trials while adhering to budget, scope and timelines. The CPM is responsible for managing all aspects of a clinical trial or multiple clinical trials including CRO & vendor selection and oversight to ensure patient safety, adherence to the contract, protocol and appropriate safety regulations and data integrity. The CPM will lead planning and communication with cross-functional study teams to ensure proper execution and conduct of the trial. Serves as primary contact and resource for vendors and the LCRA or CRO monitors.