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 Clinical Data Manager (CDM) will be responsible for all data management activities from study start up to database lock. The CDM will work on studies independently or will manage CROs & interact with outside vendors. The CDM will perform medical dictionary coding. The CDM is also responsible for creating databases and providing programming support as required.
The Clinical Trial Manager (CTM) 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. Additional responsibilities include tracking CRO activities and project status, reviewing clinical data profiles, implementing enrollment and recruitment strategies, and preparing study documents and tools. The CTM is also responsible for Investigator compliance, Investigator Site File (ISF) inspection readiness, oversight of monitoring visit scheduling, site and monitoring performance metrics, issue escalation and corrective actions. The CTM will develop study tools for sites and CRA use, review trip reports, review and track protocol deviations, and support other objectives for the clinical operations department.
This is a temporary to permanent employment opportunity as a Regulatory Affairs Specialist.
The Associate Director of Biometrics designs the statistical sections of protocols for the Company’s clinical trials. The incumbent writes or oversees the writing of statistical analysis plans. The Associate Director of Biometrics is responsible for project management and supporting the clinical group’s statistical needs with regard to data analysis; for interacting with CROs or internal programmers, and for interactions with the Drug Safety and Data Management groups. In addition, this person will be responsible for preparing statistical analyses of study-level data as required for presentations and submissions.
The Clinical Trial Assistant (CTA) is responsible for supporting the clinical project team in daily study activities and clinical trial conduct by providing administration and project tracking support.