Clinical Trial Manager

The Opportunity

Description

We're looking for a Clinical Trial Manager, working in Pharmaceuticals and Medical Products industry in 269 E Grand Ave, South San Francisco, California, 94080, United States.

Develop and contribute to study-related documents and materials (e.g. protocols, consent forms, monitoring plans, eCRF design and completion guidelines, vendor requirements, etc.)

Perform and oversee study monitoring activities, including review of monitoring reports, protocol deviations, and data listings to ensure data quality.

Manage operational aspects of clinical studies from study start-up through database lock.

Our Client

Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.

Experience Required for Your Success

Bachelors degree in health or life science, or equivalent practical experience (Advanced degree preferred)

Minimum of 6 years in clinical research project management

Strong experience with FDA regulations for clinical trials and GCP

Ability to work effectively in teams and independently

Ability to manage multiple projects at a time in a fast-moving, nimble environment

Diagnostic and/or medical device (including software as a medical device) experience

Mental health and developing digital health tools 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?