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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.

Senior Director, Process Chemistry & Manufacturing

The Senior Director will be responsible for process development of Progenics’ novel radiopharmaceutical therapeutic and imaging products. The individual will also responsible for manufacture of radiopharmaceuticals and active pharmaceutical ingredients at external Contract Manufacturing Organizations (CMOs). This is a key leadership position that will interface with various functions at Progenics as well as Progenics’ partners to ensure timely and cost-effective development and manufacturing of radiopharmaceutical drugs for clinical supply and commercial launch.

Director, Biostatistics

The Director of Biostatistics will be responsible for providing leadership and statistical input into all of the clinical development programs. He/she will be responsible for managing simultaneous projects and must have a proven track record to be flexible, proactive, and collaborate skillfully and effectively with other functional areas. He/she will oversee the programming and data management staff and must possess the ability to provide clear direction and mentorship. A hands-on approach is necessary to support the clinical group’s statistical needs with regard to data analysis, for interacting with CROs, and for preparing study-level analyses as required for presentations and submissions. He/she must have excellent writing skills and the ability to explain complex statistical results in a clear and concise manner.