We're looking for a Clinical Trial Management Associate, working in the Pharmaceuticals & Medical Products industry in Irvine, California, United States.
Supports study feasibility activities and performs database/web searches for sites as needed.
Works closely with the Site Start Up (SSU) and ensures all study related regulatory and financial documents are collected and reviewed in support of study activation.
Organizes and maintains project working files and tracks critical documents.
Reports discrepancies to the appropriate clinical team member in a timely manner.
Tracks and assists with processing site/vendor payments.
We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
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
Associate degree or higher preferred.
1-2 year relevant experience in pharmaceutical industry or CRO (Clinical Research Organization).
Experience supporting clinical trials preferred.
Basic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plus.
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.