The PCCTC Is Expanding Its Trial Management Capabilities

June 12, 2018 | Media Relations

To better meet the needs of our partners the PCCTC is expanding its infrastructure. Our central management team is now seeking an experienced Research Project Coordinator, Clinical Research Data Manager, Research Project Manager, and Administrative Project Coordinator to help fulfill our mission to design, implement and complete hypothesis-driven early phase trials in prostate cancer, translating scientific discoveries to improved standards of care. Follow the links in the titles below for full job descriptions and application information.

 

Research Project Coordinator
As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the Research Project Coordinator is responsible for providing support to the Clinical Operations team for multi-center clinical trial activities from concept to close-out.

 

Clinical Research Data Manager
The Data Manager provides requirements specifications for instrument design (eCRFs/databases, edit checks) for data acquisition for clinical trials performs data cleaning activities to review, analyze and validate data to ensure completeness, integrity and accuracy. Commitment to accuracy, high attention-to-detail, and ability to work independently are critical competencies for the role.

 

Research Project Manager (IRONMAN)
The Research Project Manager is responsible for providing support to the Clinical Operations Program Manager and Chief Executive Officer for multi-center clinical trial activities specific to the IRONMAN Registry.

 

Administrative Project Coordinator
The Administrative Project Coordinator is responsible for providing support to the Clinical Operations (CO), Clinical Data Management (CDM), Business Operations (BO), Editorial, Regulatory/Quality and Chief Executive Officer (CEO) for multi-center clinical trial activities from concept to close-out.

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Our services translate scientific discoveries into improved standards of care, ensuring efficient trial selection, reporting, site management, clinical operations and data analyses.