What are the responsibilities and job description for the Clinical Trial Assocaite position at Redbock - an NES Fircroft company?
CLINICAL TRIAL ASSOCIATE (12-month, Possibility of extension and/or conversion)
SUMMARY:
Clinical Trial Assistant needed for consultant assignment supporting TMF and audit activities for cutting-edge biotech innovator
DUTIES & RESPONSIBILITIES:
* Electronic Trial Master File management and quality control
* Clinical document quality review and organizing
* Support vendor contracting and documentation
* Tracker and Database support
* Additional Clinical Trial and Clinical Operations support, as needed
QUALIFICATIONS & REQUIREMENTS:
* 2 years of relevant Clinical Operations experience as a Clinical Trial Associate, Clinical Trial Assistant, Clinical Project Coordinator, or equivalent for pharmaceutical sponsor companies
* Proven experience managing and QC-ing eTMFs and related electronic and paper clinical documents
* Excellent attention to detail
* Excellent written, verbal and interpersonal communication skills, and computer skills, including Microsoft Office
LOCATION:
Work will be performed onsite in the greater San Francisco Bay Area. Professionals who live outside the area, but have proven experience working successfully from home, may be considered for remote work.
