Bristol Myers Squibb (BMS) is a global biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a mission to transform patients’ lives through science, BMS fosters a culture of passion, innovation, urgency, accountability, inclusion, and integrity.
Working at BMS means engaging in uniquely interesting and life-changing work every day. From cutting-edge cell therapy breakthroughs to optimizing clinical trials, BMS employees contribute to advancements that redefine patient care worldwide.
Job Description
Position Summary
As a Global Trial Specialist (GTS) at Bristol Myers Squibb, you will play a crucial role in the operational execution of global clinical trials. You will collaborate with cross-functional teams to ensure smooth study conduct from protocol development to final clinical study reporting. This role involves managing study-level documentation, supporting trial management systems, and ensuring compliance with regulatory standards.
Key Responsibilities
- Assist in the operational execution of clinical studies, supporting complex global trials.
- Contribute to study planning, including timelines, documentation, and regulatory submissions.
- Manage country planning, protocol-level attributes, and milestones in Clinical Trial Management Systems (CTMS).
- Ensure accuracy and completeness of the electronic Trial Master File (eTMF).
- Coordinate global setup of non-clinical trial supplies.
- Facilitate vendor payments and regulatory submissions.
- Participate in study team meetings, capturing minutes, and tracking action items.
- Identify risks, develop mitigation strategies, and escalate issues as needed.
Qualifications & Experience
- Education: BA/BS or Associate degree in a relevant discipline.
- Experience:
- Prior experience in clinical research or related fields.
- Familiarity with Clinical Trial Management Systems (CTMS) and Trial Master File (TMF) systems is a plus.
- Global clinical trial exposure is advantageous.
- Skills:
- Basic knowledge of ICH/GCP and regulatory guidelines.
- Understanding of clinical research budgets and vendor payments.
- Strong communication, collaboration, and problem-solving abilities.
Why Join Bristol Myers Squibb?
- Impactful Work: Contribute to life-changing therapies for patients worldwide.
- Career Growth: Access to unparalleled professional development opportunities.
- Flexible Work Environment: Hybrid work options for eligible roles.
- Inclusive Culture: A workplace that values diversity, equity, and inclusion.
