We're looking for a Clinical Records Associate, working in the Biotechnology/Medical Devices industry in Foster City, California, United States.
Maintain a minimal understanding of GCP, ICH and GLP regulations associated with the maintenance and retention of clinical trial documentation and preclinical study records.
Participate in continued security and maintenance of the Trial Master File (TMF) Room.
Participate in offsite storage activates.
Create and maintain study-specific file structures for client's clinical, biometrics, and preclinical documents and file documents accordingly.
Ensure record filing is kept up to date and is performed accurately.
The pay range we're offering is 40 to 43 per hour. This position may present an opportunity to go permanent.
Our client is a people driven staffing company. Growing fast - 33% annually!
How? Building trusting relationships with top candidates. Like you! You’ll get one-on-one time focused on your skills, needs, and discovering opportunities in which you’ll thrive. The goal is to place you in the right position for you and your goals.
Where? Top IT and telecommunications companies. You’ll make a difference and grow in Technology, Government Services, Professional Services, or Engineering.
Helping you achieve your goals! It’s the right way and the only way to succeed in staffing.
Experience Required for Your Success
TMF experience (Paper)
Knowledge of 1572 form
MS Excel experience
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.