BMS Clinical Trial Support Specialist Job Opening, Apply Online
Bristol Myers Squibb (BMS) is a global biopharmaceutical company headquartered in New York City, dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. Established through the 1989 merger of Bristol-Myers Company and Squibb Corporation, BMS focuses on therapeutic areas such as oncology, immunology, cardiovascular, and fibrotic diseases.
Experience uniquely interesting work that is challenging, meaningful, and life-changing at Bristol Myers Squibb. We value diversity and offer opportunities uncommon in scale and scope. Join us to help transform patients’ lives through science.
Job Posting: Clinical Trial Support Specialist
- Time type: Full time
- Posted on: Posted Yesterday
- Job requisition id: R1590578
Position Responsibilities:
- Streamlining the Clinical Trial documents process in collaboration with the Submission Manager
- Preparing submission documents in adherence to regulatory guidelines
- Creating site numbers for new and ongoing clinical trials
- Ensuring accuracy of data in Veeva (eTMF/CTMS)
- Managing interactions with multifunctional teams across the oncology portfolio
Experience Requirements:
- 2-4 years of relevant experience in clinical trial documentation management
- Demonstrated knowledge of ICH/GCP and regulatory guidelines
- Experience with industry Clinical Trial Master File Systems or equivalent
If you come across a role that intrigues you but
doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.On-site Protocol:
BMS offers various occupancy types, ensuring roles are performed effectively based on responsibilities. On-site roles require 100% onsite presence, while hybrid roles may have at least 50% on-site work.
BMS is dedicated to ensuring equal employment opportunities and supports workplace accommodations for people with disabilities. Vaccination against Covid-19 is strongly recommended for all employees.
If you have any inquiries or require workplace accommodations, contact [email protected].
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