We are looking for a Clinical Data Coordinator, working in the Pharmaceuticals & Medical Products industry in Woodcliff Lake, New Jersey, United States.
Performs QC, reconciliation of different study files and reports, reconciliation of EDC and IRT user access against training records, and other tasks as needed.
Uploads clinical study documents to TMF Systems.
Performs CIOMS redaction
Performs QC of various documents
Verifies and reconciles EDC & IRT access
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
Bachelor's degree in Sciences, Computer Sciences or other fields
Knowledge of TMF, EDC, or proficient in operating basic computer systems
Ability to learn new computer systems
Knowledge and understanding of the clinical development process is a plus
Knowledge and understanding of GCP 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.