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Clinical Data Manager
Ref No.: 15-05424
Location: Audubon, Pennsylvania
Position Type:Contract
Our client is hiring a Clinical Data Manager to be located in the greater Philadelphia area!
Submit resume for immediate consideration directly to Tara Brabham by clicking the link below. I can also be reached at 813-443-2363 with questions.
**We offer a lucrative referral bonus**

The Clinical Data Manager is responsible the coordination of internal and external data management activities and resources supporting the clinical trials data management activities by:
  • Conducting manual data review and coding for data management customers
  • Ensuring that study database is appropriately cleaned in accordance with agreed upon data management plan
  • Developing project specific edit check specifications
  • Carrying out data management UAT prior to release to the customer
  • Assisting in the development of and compliance to study/client specific data management plans
  • Managing clinical data reviewers for each assigned data management project
The Clinical Data Manager also ensures client satisfaction and data integrity by:
  • Working with data management team, and data management customers to assure that their data are effectively managed.    
  • In conjunction with reports programmers, develops project specific reports for metrics and database cleaning.
  • Working in conjunction with study team in developing forms package for use in the development of the study.
  • Ability to work in group setting and independently; ability to adjust to changing priorities.
  • Excellent attention to detail and orientation toward meticulous work.
  • Strong interpersonal and communication skills, both verbal and written.
  • Strong documentation and organizational skills.
  • Ability to project and maintain a professional and positive attitude.

  • Associate's degree required, Bachelor's preferred, in the life sciences or a related field.
  • 3+ years data management experience, preferably in a CRO or similar field.
  • Understanding of medical and/or clinical trial terminology required.
  • Proven ability in analyzing data.
  • Experience working with computer software including Word, Excel and Access preferred.
  • 2+ years experience working with clinical trials and/or within pharmaceutical environment preferred.