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Associate Global Trial Manager

2+ years
Not Disclosed
10 Aug. 14, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Description

Working with Us

At Bristol Myers Squibb, we don’t just offer jobs—we offer opportunities for impactful and transformative work. Every role here contributes to groundbreaking advancements, from enhancing production processes to pioneering cell therapy breakthroughs. Join us to be part of a team where your work not only transforms patients' lives but also shapes your career in ways you never imagined.

We value balance and flexibility, offering a range of competitive benefits and programs to support your career and personal goals. Discover more about working with us at careers.bms.com/working-with-us.

Position: Associate Global Trial Manager

Division: Research and Development

Position Summary

As an Associate Global Trial Manager at Bristol Myers Squibb, you will play a crucial role in overseeing the operational aspects of complex, global clinical trials. From inception through to the final report, you will manage various phases of clinical trials, ensure adherence to project management standards, and collaborate with internal and external stakeholders to deliver results.

Key Responsibilities

  • Project Management:

    • Support study execution using performance metrics and quality indicators.
    • Oversee clinical monitoring quality and adherence to established processes.
    • Manage study deliverables and timelines, making data-driven decisions.
    • Identify and address potential risks, ensuring timely and effective solutions.
    • Maintain and implement project management tools and documentation.
  • Study Planning and Conduct:

    • Oversee the set-up and quality review of study documents and TMF.
    • Provide operational input into study documents and plans.
    • Support site feasibility, recruitment strategies, and protocol adherence.
    • Manage vendor relations, review invoices, and handle budget matters.
  • Leadership and Team Collaboration:

    • Encourage cross-functional teamwork and maintain a focus on project objectives.
    • Provide guidance to Global Trial Specialists and foster a collaborative environment.
    • Adapt to changing business needs and motivate team members.

Qualifications

  • Education: Bachelor’s degree in a relevant field. Master’s degree preferred.
  • Experience: Minimum 2 years in clinical study management or related experience, with demonstrated project management skills in the pharmaceutical or healthcare industry. Familiarity with CTMS systems is a plus.
  • Skills:
    • Strong knowledge of ICH/GCP, regulatory guidelines, and clinical research processes.
    • Proficiency in Microsoft Office Suite.
    • Ability to manage multiple priorities, adapt to shifting demands, and foster teamwork.
    • Excellent interpersonal, problem-solving, and communication skills.

Additional Information

  • On-site Protocol: The role may require on-site presence based on the nature of the job. Roles may be site-essential, site-by-design, field-based, or remote-by-design.
  • Diversity and Inclusion: We are committed to providing reasonable accommodations and support for all applicants. If you need assistance during the recruitment process, please contact adastaffingsupport@bms.com.

At Bristol Myers Squibb, every role contributes to our mission of transforming patients' lives through science. We encourage you to apply, even if your experience doesn't align perfectly with the role, as you might be just the person we’re looking for.

For more information and to apply, visit careers.bms.com.