We're looking for an Associate Director of Clinical Data Management, working in the Biotechnology/Medical Devices industry in Alameda, California, United States.
Oversees, develops and manages clinical data management activities while collaborating and coordinating with other departments.
Oversees the evaluation, integration and implementation of new clinical systems and technologies for clinical trial management activities including electronic data capture and documentation systems.
Provides a high level of expertise in data management to support clinical studies, including areas such as: Case Report Form (CRF) design, database design, data management plans, edit checks/quality review plans, query resolution processes, data transfers, SAE/AE reconciliation, thesaurus coding processes, and database lock.
Manages time and resource constraints across multiple projects.
Develops and implements new or improved processes for data management.
We are offering Competitive Compensation and Benefits.
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
BS/BA degree in related discipline and 13 years of related experience; or, MS/MA degree in related discipline and 11 years of related experience; or, PhD in related discipline and 8 years of related experience, or; equivalent combination of education and experience, may require certification in assigned area
Minimum of 14 years of experience in clinical data management
Minimum of 7 years of line management experience is required
Demonstrated experience leading data management teams is required
Experience participating in regulatory submissions and inspections is required
Oncology experience is a must
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.