Job Title: Document Coordinator - Clinical Trials
Location: [Insert Location]
Category: Clinical Research
Job ID: [Insert Job ID]
Position Summary:
As a Document Coordinator at Bristol Myers Squibb, you will play a vital role in managing clinical trial-related documents across all phases of global clinical trials. This includes the collection, compilation, review, and approval of essential documents, as well as addressing site monitoring reports, issue escalation, and follow-up. You will serve as the main point of contact for clinical documentation, regulatory submissions, and support for the study team throughout the trial lifecycle.
Key Responsibilities:
Qualifications & Experience:
Company Overview:
At Bristol Myers Squibb, we are united by a vision of transforming patients' lives through science. Our work goes beyond the ordinary, empowering employees to bring their unique talents and perspectives to an inclusive culture, where diversity in clinical trials is celebrated. Our core values of passion, innovation, urgency, accountability, inclusion, and integrity drive us to achieve our highest potential.
On-site Protocol:
BMS has a diverse occupancy structure. Depending on your role, you may be required to work onsite, in a hybrid model, or remotely. The nature of the role will dictate your work location type.
Equal Opportunity Statement:
Bristol Myers Squibb is committed to creating an inclusive environment and ensuring equal employment opportunities for all individuals. We encourage applicants from all backgrounds and offer accommodations to those who need them during the recruitment process.
How to Apply:
Learn more and apply through the Bristol Myers Squibb careers portal: BMS Careers.
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