Associate Director, External Data Acquisition

2 days ago

Princeton, New Jersey, United States Bristol-Myers Squibb Company Full time
Transforming Patients' Lives through Science

Bristol Myers Squibb is a global biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking an experienced Associate Director, External Data Acquisition to join our team.

Job Summary

The Associate Director, External Data Acquisition will be responsible for leading the acquisition and integration of external clinical trial data across multiple programs. This role will oversee a team of professionals in planning, set-up, acquisition, and integration of external clinical trial data.

Key Responsibilities
  • Provide leadership and oversight of external clinical data acquisition and integration activities
  • Drive data collection and integration strategies for vendor/partner-generated clinical trial data
  • Ensure adaptive management of a global team through effective resource deployment and streamlined processes
  • Manage the book of work for initial and post-production external clinical trial data activities
  • Assign resources to studies and initiatives and monitor workloads to avoid delays
  • Forecast future resource needs based on the book of work
  • Provide ongoing feedback, coaching, and career development to staff
  • Empower and hold staff to high-quality performance and delivery
  • Ensure procedural documents are reflective of industry standards and regulatory requirements
  • Contribute to the development and application of smart systems and optimal approaches to support data collection
  • Hold accountability to resolve complex issues and proactively develop solutions
  • Lead continuous improvement activities and implement changes to create industry-leading external data capabilities
  • Represent the function for Health Authority inspections and internal audits
  • Engage and energize employees through communication of goals, priorities, and business-critical information
  • Develop and promote a workplace culture that values diversity of thought, promotes integrity, and fosters accountability
  • Ensure effective quality oversight and management of external partners performing external data acquisition activities
  • Develop strong and productive working relationships with key stakeholders throughout GDM&CM, GCO, and BMS
  • Represent the Company in interactions with key external partners as part of any committee or industry group relating to external data
Requirements
  • Bachelor's degree required with an advanced degree preferred
  • At least 7 years of global clinical trial expertise with a focus on external clinical data acquisition and integration
  • Successful track record of leading through influence, working across complex, global organizational matrices, and effectively managing staff
  • Deep understanding of the drug development process and clinical trial start-up/execution
  • Proven expertise in external data acquisition and integration processes and technologies
  • Strong knowledge of industry-leading external data acquisition tools and well-versed in industry trends and emerging technologies supporting data acquisition
  • Strong knowledge of GCP/ICH guidelines
  • Proven record of proactively resolving complex issues, making decisions with an enterprise mindset, and driving significant initiatives to completion
  • Technical expertise, technical writing ability, and proficiency in Systems Development LifeCycle (SDLC) principles
  • Demonstrated partnership across various collaborative and industry forums
  • Diverse and sufficient technical expertise to be a credible interface to all global development and business partners
  • Influential leadership and communication capabilities with a proven ability to engage, manage, develop, and inspire a geographically diverse team

Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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