Clinical Trial Job at Bristol Myers Squibb, Hyderabad | Apply Now for Global Trial Acceleration Associate Role
Join Bristol Myers Squibb as a Global Trial Acceleration Associate in Hyderabad, where you will contribute to life-changing clinical research. This Job at Bristol Myers Squibb involves managing centralized activities that support global clinical trials, emphasizing clinical documentation, regulatory submissions, and collaboration with cross-functional teams. Take part in transforming patient lives through science while building a rewarding career in global clinical operations.
Job Details:
- Position: Global Trial Acceleration Associate
- Location: Hyderabad, Telangana, India
- Company: Bristol Myers Squibb (BMS)
- Employment Type: Full-time
- Category: Clinical Operations / Global Trials
- Experience Required: Minimum 3 years in clinical development or operations (Pharma/Biotech/CRO)
About the Company:
Bristol Myers Squibb (BMS) is a global biopharmaceutical leader dedicated to transforming patients’ lives through science. At BMS, you’ll experience meaningful, challenging, and life-changing work that drives innovation and scientific excellence. The company fosters a culture of collaboration, inclusion, and accountability, offering opportunities for personal and professional growth while contributing to advancements in healthcare and medicine worldwide.
Educational Requirements for this Clinical Trial Job:
- Bachelor’s degree in Life Sciences, Business Administration, or Legal Studies (or equivalent).
- Advanced degree is considered an advantage.
- Minimum 3 years of relevant experience in clinical development or operations within the pharmaceutical, biotechnology, or CRO sectors.
Key Responsibilities for this Clinical Trial Job:
- Manage and execute centralized activities supporting global clinical trials, focusing on clinical documentation.
- Serve as the primary contact for essential document management and regulatory submissions.
- Support outsourcing, vendor management, and contracting for outsourced studies.
- Initiate and manage start-up documentation activities for global clinical trials.
- Oversee country/site activation, document review, and quality control of start-up processes.
- Maintain and update clinical systems such as CTMS, eTMF, and vendor systems.
- Coordinate translation, review, and distribution of study-level documentation.
- Ensure ongoing maintenance and collection of essential documentation across study phases.
- Collaborate with study teams and stakeholders to ensure compliance and efficiency in clinical operations.
Skills Required for this Clinical Trial Job:
- Strong knowledge of ICH/GCP guidelines and regulatory standards.
- Hands-on experience with regulatory submissions, IRB/IEC documentation, and clinical trial start-up processes.
- Experience using CTMS, eTMF, Veeva Vault, MS Office, and SharePoint.
- Effective communication and stakeholder management skills.
- Excellent organizational, analytical, and decision-making abilities.
- Proven ability to manage cross-functional, multicultural teams.
- Adaptability and time management skills in a dynamic environment.
How to Apply for this Clinical Trial Job at BMS?
Interested candidates can apply through the official Bristol Myers Squibb Careers page. Candidates are encouraged to review the job requirements carefully and submit an updated resume for consideration.
