Lead and manage data management activities for assigned products, initiatives and/or clinical trials
Design clinical trial databases, including CRF Development, Database Validation, and Data Review tools
Oversee external data management vendors
Optimize data management and collection activities
Maintain current knowledge of relevant issues related to data management
Propose, draft, and maintain relevant Standard Operating Procedures
Act in accordance with Company policies

Bachelor’s degree in a scientific, medical, computer science or related field; Master’s degree preferred
A minimum of 5 years’ management level experience in a pharma or biotech environment
Strong experience in data management-related activities
Thorough understanding of the clinical trial process and regulatory requirements, including CDISC
Strong experience in design and validating EDC databases and performing data review
Familiar with safety laboratory data management and dictionary coding for adverse events and medications
Experience in CNS, pediatric rare disease area and e-diary database design and implementation are preferred
Experience in CRO management
Ability to be hands-on with database cleaning
Excellent leadership and interpersonal skills
Proven ability to collaborate in high performing teams
Ability to travel up to 10%, both domestically and internationally.

Senior Manager, Data Management

Key skills