Bristol-Myers Squibb

Executive Director, Global Trial Management

Bristol-Myers Squibb

Princeton, NJ, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Are you a seasoned leader with a passion for driving successful global clinical trials? Do you have experience managing complex projects and cross-functional teams? Bristol-Myers Squibb is seeking an Executive Director of Global Trial Management to join our dynamic team. In this role, you will play a critical role in overseeing and directing all aspects of global clinical trial execution, ensuring the timely and high-quality delivery of clinical trial data. We are looking for a driven and strategic individual who can thrive in a fast-paced environment and make a significant impact in the advancement of our pipeline. If you have a strong background in clinical trial management and a desire to make a difference in the lives of patients, we want to hear from you.

  1. Lead and oversee all aspects of global clinical trial execution, including study design, planning, implementation, and close-out.
  2. Manage and coordinate cross-functional teams to ensure efficient and effective clinical trial operations.
  3. Develop and implement strategic plans for global clinical trials, including timelines, budgets, and resource allocation.
  4. Drive the successful delivery of high-quality clinical trial data within specified timelines.
  5. Establish and maintain relationships with key stakeholders, including internal teams, external vendors, and regulatory agencies.
  6. Monitor and track progress of clinical trials, identifying potential risks and implementing mitigation strategies.
  7. Ensure compliance with all applicable regulations and guidelines, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) standards.
  8. Collaborate with other departments, such as Regulatory Affairs and Medical Affairs, to support the development and submission of clinical trial protocols and reports.
  9. Provide leadership and mentoring to team members, fostering a culture of continuous learning and development.
  10. Stay abreast of industry trends and best practices in clinical trial management and incorporate them into the company's processes and procedures.
  11. Effectively communicate updates and progress to senior management and other stakeholders.
  12. Represent the company at conferences, meetings, and other external events related to clinical trial management.
  13. Contribute to the development of departmental and company-wide strategies to support the advancement of the company's pipeline.
  14. Act as a role model for ethical and professional behavior, promoting a culture of integrity and compliance within the organization.
  15. Continuously assess and improve processes and procedures to enhance efficiency and quality in clinical trial management.
Where is this job?
This job is located at Princeton, NJ, USA
Job Qualifications
  • Advanced Degree In Life Sciences Or Related Field: A Minimum Of A Master's Degree In A Relevant Field Is Required For The Executive Director, Global Trial Management Role At Bristol-Myers Squibb. This Advanced Education Provides The Necessary Foundation And Knowledge For Overseeing Global Clinical Trials.

  • Extensive Experience In Clinical Trial Management: The Ideal Candidate Should Have At Least 10 Years Of Experience In Managing Global Clinical Trials, Including Experience In Both Early And Late-Stage Trials. This Experience Should Include A Strong Track Record Of Successful Trial Execution And Management Of Cross-Functional Teams.

  • Strong Leadership Skills: The Executive Director, Global Trial Management Will Be Responsible For Leading And Managing A Team Of Clinical Trial Professionals, Therefore Strong Leadership Skills Are Essential. This Includes The Ability To Effectively Communicate With Team Members, Motivate And Inspire Others, And Make Tough Decisions When Necessary.

  • In-Depth Knowledge Of Regulatory Requirements: A Deep Understanding Of Global Regulatory Requirements And Guidelines Is Crucial For This Role. The Executive Director Must Have A Strong Understanding Of The Regulatory Environment And Be Able To Navigate And Interpret Complex Regulations In Order To Ensure Compliance With All Applicable Laws And Regulations.

  • Strategic Thinking And Business Acumen: The Executive Director, Global Trial Management Will Play A Critical Role In Developing And Executing The Company's Clinical Trial Strategy. Therefore, The Ideal Candidate Should Possess Strong Strategic Thinking Skills And Business Acumen. They Should Be Able To Identify And Anticipate Potential Challenges And Opportunities And Develop Innovative Solutions To Drive Success.

Required Skills
  • Strategic Planning

  • Project Management

  • Contract Negotiation

  • Budget management

  • Leadership

  • Team Building

  • Risk assessment

  • Regulatory compliance

  • Stakeholder engagement

  • Cross-Functional Collaboration

  • Clinical Trial Operations

Soft Skills
  • Communication

  • Emotional Intelligence

  • Leadership

  • Time management

  • Interpersonal Skills

  • creativity

  • Critical thinking

  • Teamwork

  • Adaptability

  • Problem-Solving

Compensation

According to JobzMall, the average salary range for a Executive Director, Global Trial Management in Princeton, NJ, USA is $200,000 - $250,000 per year. However, this can vary depending on the specific company, industry, and level of experience of the individual.

Additional Information
Bristol-Myers Squibb is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedMay 21st, 2024
Apply BeforeMay 10th, 2026
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About Bristol-Myers Squibb

Bristol-Myers Squibb Co. operates as a biopharmaceutical company, which engages in the discovery, development, licensing, manufacturing, marketing, distribution, and sale of biopharmaceutical products. It includes chemically-synthesized drugs or small molecules and products produced from biological processes called biologics.

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