Pharmaceutical Data Manager:

Princeton New Jersey

Our client is looking for a Manager, of Pharmaceutical Data Management who will maintain a project-level perspective on data management issues, activities and deliverables. You will oversee the Contract Research Organization (CRO) and third-party vendor processes involved in developing data collection systems, data cleaning and providing data deliverables conforming to global CDISC standards.

Successful candidates will have:

  • Bachelor's degree
  • 3 years' of Pharma data management (i.e., clinical data)
  • 3+ years' Project Management experience and skills
  • Strong understanding of medical concepts and terminology
  • Experience providing expert review and assistance in the development of CRF/eCRF/eSource design specifications, validation specifications and report design, etc.
  • Esource experience, nice to have but other comparable experience will be helpful
  • Knowledge of CDISC and industry standards
  • Strong working knowledge of data management practices and applicable global regulatory requirements
  • Strong working knowledge of electronic data capture systems, eSource and familiarity with regulatory guidelines on use of electronic systems.
  • Strong computer skills with demonstrated experience in working with the Microsoft suite of programs.
  • Ability to determine how/when to apply organizational policy or procedures to a variety of situations.
  • Excellent written and verbal communication/presentation skills.

The position is WFH (Eastern Time zone) during the Covid crisis; however candidates will be work in Princeton, NJ (post Covid). This is a long-term consulting assignment-initial contract of 12 months, with extensions likely. Compensation is DOE.

Please advise if you or someone you know is interested.

No subcontracting allowed.

All the Best,