Looking for the latest Clinical Trial Support Specialist jobs in Hyderabad? Bristol Myers Squibb (BMS) has announced a new opportunity for professionals interested in clinical operations, regulatory documentation, and clinical trial support. This full-time position offers an opportunity to work with one of the world’s leading biopharmaceutical companies supporting global clinical trials.

If you have experience in clinical research, clinical trial documentation, CTMS, eTMF, Veeva Systems, GCP, ICH Guidelines, and regulatory submissions, this could be an excellent opportunity to build your career in the pharmaceutical industry.

Job Overview

About Bristol Myers Squibb

Bristol Myers Squibb (BMS) is a globally recognized biopharmaceutical company committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company offers excellent career growth, global exposure, competitive compensation, and opportunities to work on life-changing clinical research programs.

Clinical Trial Support Specialist Job Responsibilities

The selected candidate will support global clinical trial operations by managing documentation, regulatory submissions, and operational activities.

Key Responsibilities

• Prepare clinical trial submission documents according to regulatory requirements.
• Ensure all documents are Submission Ready Compliant (SRC).
• Partner with Submission Managers for document preparation and submission timelines.
• Create and maintain Clinical Study Report (CSR) appendices.
• Prepare Financial Disclosure Tables and regulatory documentation.
• Support clinical trial document management using Veeva platforms.
• Coordinate creation of site numbers for new and ongoing studies.
• Maintain clinical trial milestones and regulatory approval records.
• Ensure accurate drug shipment information for SAP integration.
• Reconcile Veeva eTMF and CTMS data for accuracy.
• Resolve operational issues using critical thinking.
• Support compliance with company SOPs and global regulatory requirements.
• Collaborate with cross-functional teams across oncology and other therapeutic areas.
• Assist in document management throughout the clinical trial lifecycle.
• Perform additional clinical operations support activities as assigned.

Required Skills

Candidates with experience in the following areas will have an advantage:

• Clinical Trial Management
• Clinical Operations
• Clinical Documentation
• Regulatory Submissions
• CTMS
• eTMF
• Veeva Vault
• Good Clinical Practice (GCP)
• ICH Guidelines
• Clinical Study Reports (CSR)
• Financial Disclosure Documentation
• SAP
• Regulatory Compliance
• Project Management
• Problem Solving
• Pharmaceutical Industry Knowledge
• Cross-functional Collaboration

Preferred Qualifications

BMS has not specified mandatory educational qualifications in the job posting. However, candidates from the following backgrounds are generally suitable:

• B.Pharm
• M.Pharm
• Pharm.D
• BSc Life Sciences
• MSc Life Sciences
• Biotechnology
• Clinical Research
• Biomedical Sciences
• Nursing
• Related Healthcare or Life Science disciplines

Relevant experience in clinical research, clinical operations, or clinical documentation will be preferred.

Why Join Bristol Myers Squibb?

Working at Bristol Myers Squibb offers several benefits including:

• Competitive salary package
• Performance-based incentives
• Global career opportunities
• Hybrid work environment
• Professional development programs
• Exposure to international clinical trials
• Inclusive workplace culture
• Learning and leadership development
• Comprehensive employee benefits
• Opportunity to contribute to life-changing medicines

Expected Salary

Based on similar Clinical Trial Support Specialist positions in Hyderabad, the estimated annual salary is:

₹8,00,000 – ₹15,00,000 per annum (CTC)

Actual compensation depends on experience, skills, and interview performance.

Location

Hyderabad, Telangana, India

How to Apply

Application Link