We're looking for a Clinical Research Associate II, working in the Biotechnology/Medical Devices industry in Pleasanton, California, United States.
Ensures site compliance with regulations and study protocol.
Ensures accurate and complete study management/data collection and transfer to data management.
Manages material logistics for the studies.
Reviews study protocols, reports and manuscripts and contributes technical and clinical operations expertise for documents.
Works with Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites.
We're 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
Bachelor's degree in scientific discipline or related field.
2 plus years of experience in clinical study coordination, clinical site monitoring or clinical study management is required.
Prior experience with current Good Clinical Practices (cGCP) and Code of Federal Regulations (CFR) is preferred.
A background in biomedical/healthcare services with laboratory experience preferred.
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.