We are looking for a Clinical Scientist, working in the Pharmaceuticals & Medical Products industry in Pearl River, New York, United States.
To become familiar with trial related materials and reporting systems.
Reads redacted clinical serious adverse events reports and scanned medical charts documents and compared against information in an electronic case report form.
Submits electronic queries to site staff related to key discrepancies.
Reviews site staff responses to see if adequate.
Facilitates the reporting of unreported safety events or infections as per trial protocol.
Meets with clinical scientist/medical monitor to review and oversee work performed.
The pay we are offering is 28 per hour. 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
Clinical training such as medicine or nursing required to allow for understanding and interpretation of clinical documents
Must have data review experience
No license to practice in US required
Past experience in clinical data review and clinical trials a plus but not required
Basic computer skills to facilitate learning key study-specific data systems
Minimum education experience required:
BA/BS Degree in science or health-related field
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.