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Global Document Manager

2 weeks ago

Hyderabad, Telangana, India Bristol-Myers Squibb Full time

We are seeking a highly organized and detail-oriented Global Document Manager to join our Clinical Development team at Bristol-Myers Squibb. In this role, you will be responsible for managing and executing start-up documentation activities for global clinical trials, developing and maintaining collaborative working relationships with clinical investigator sites, and supporting outsourcing activities by interfacing with operational teams, support groups, and service providers.

Responsibilities
  • Initiate and manage start-up documentation activities for global clinical trials
  • Generate, process, track, and distribute Confidential Disclosure Agreements (CDAs)
  • Provide input into the creation of feasibility questionnaires, distribution, and tracking

You will serve as the single point of contact for the study team for centralized activities during study start-up, ongoing maintenance, and tracking of essential documentation, collection of updated outstanding documentation, and submission to Regulatory as required.