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Clinical Data Manager

  • Job type: Permanent
  • Location: San Francisco
  • Salary: $130000 - $145000 per annum, Benefits: Commuter Benefits; Food provided On-site;
  • Job reference: 0314GB18
  • Sector: Clinical Development, Clinical, Clinical Operartions, EPM Scientific
  • Date posted: 14/04/2018
The clinical data manager will be joining the fast-paced Clinical Data Management and Bio-statistics team. With a new group coming together and a clear goal for study direction, you will be providing support for everyday clinical data functions in order to push study timelines across and ultimately create a product that has the potential to completely change the Biotech Industry

The company is looking to grow fast and reach global status, and in doing so, you will be working with the top professional coming from both the pharmaceutical and medical device industries. The diverse backgrounds of everyone on the team illustrate a genuine and pure biotech culture bent on making huge advancements in health care. 

Responsibilities:
  • Manage data activities for Phase I-IV clinical trials as well as the design, review, and validation of the clinical database to deliver data for analysis and submission as part of a regulatory filing.
  • Design case report forms (CRF's) as well as data edit checks and aggregate check specifications with CRO's.
  • Be the primary liaison with CRO's for any data management related activities.
  • Participate in cross-functional team meetings (bio-statisticians and programmers)
  • Work closely with the clinical operations team to drive results in fast-paced, start-up environment
  • Manage multiple and varied tasks, prioritize workload with attention to detail
Qualifications:

  • 5+ years of clinical data management experience 
  • Bachelor's Degree is required 
  • Previous experience with managing Vendors and CROs
  • Strong understanding of EDC and clinical trial processes
  • Experience with data programming tools and/or data viewing tools (J-Review, SAS JMP.etc).

Preferred: 
  • Medical device or Pharmaceutical industry experience
  • Global trial experience 
  • High attention to detail 
  • A degree of flexibility for taking on non-traditional CDM functions (very important in a start-up environment)
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