Bristol Myers Squibb Hiring Clinical Trial Support Specialist - Hyderabad
Are you seeking high-paying BMS Careers Hyderabad or Clinical Trial Support Specialist vacancies? Leading global biopharmaceutical firm Bristol Myers Squibb (BMS) has announced recruitment for a Clinical Trial Support Specialist at its Hyderabad facility. This is a full-time, hybrid (Site-by-Design) position.
Selected candidates will manage documentation, coordinate regulatory submissions, track study milestones, and work with advanced Veeva systems. To make sure your profile is updated correctly, read our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Position | Clinical Trial Support Specialist |
| Company | Bristol Myers Squibb (BMS) |
| Location | Hyderabad, Telangana, India |
| Work Model | Site-by-Design (Hybrid as per company policy) |
| Employment Type | Full-Time |
| Job ID | R1602785 |
| Department | Clinical Operations |
| Experience Required | Relevant clinical operations, eTMF, or clinical trials documentation experience preferred (Open to various experience levels) |
| Education Background | B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotech, Clinical Research |
| Estimated Salary | ₹8.0 - ₹15.0 LPA (Based on experience) |
💼 Clinical Trial Support Specialist Key Responsibilities
- Prepare, verify, and manage clinical trial regulatory submission documents to ensure quality standards.
- Ensure all clinical documents are Submission Ready Compliant (SRC) prior to delivery.
- Partner with Submission Managers to monitor document preparation timelines and deliverables.
- Create and maintain Clinical Study Report (CSR) appendices for submission.
- Prepare Financial Disclosure Tables and related trial documentation.
- Maintain and manage clinical trial databases using Veeva Vault platforms.
- Coordinate creation of site numbers for new and ongoing research trials.
- Track study milestones, regulatory approvals, and record archives.
- Verify drug shipment data for integration into SAP platforms.
- Perform reconciliation of data between Veeva eTMF and CTMS tools.
- Apply critical thinking and problem-solving to resolve operational trial issues.
- Ensure compliance with standard operating procedures (SOPs) and global regulatory rules.
If you want to compare pharmacovigilance and drug safety salaries in private sectors, read our detailed analysis on Pharmacovigilance Salary: India vs USA.
🎓 Qualifications & Experience Requirements
BMS has not specified mandatory educational qualifications, but candidates with the following profiles are highly suitable:
- Eligible Backgrounds: B.Pharm, M.Pharm, Pharm.D, B.Sc / M.Sc Life Sciences, Biotechnology, Clinical Research, Biomedical Sciences, Nursing, or related scientific fields.
- Experience: BMS has not specified a strict number of years of experience in the official posting. However, candidates with prior experience, internships, or training in clinical trial operations, documentation management (eTMF, CTMS), or study coordination are highly preferred.
For pharmacy graduates mapping their growth paths between administrative government roles and corporate drug development careers, read our comparison guide on B.Pharm Careers: India vs USA.
Required Core Skills
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines.
- Familiarity with clinical documentation platforms (Veeva Vault, CTMS, eTMF).
- Experience in creating Clinical Study Reports (CSR) or Financial Disclosure forms.
- Familiarity with SAP or integrated supply tracking systems.
- Excellent written/verbal communication and cross-functional collaboration.
- Strong problem-solving and project management skills.
💰 Salary & Employee Benefits
- Estimated annual salary package of ₹8,00,000 – ₹15,00,000 CTC depending on skills and experience.
- Professional exposure to global clinical trials and international research frameworks.
- Hybrid working environment under the BMS Site-by-Design model in Hyderabad.
- Structured learning and leadership development programs.
- Comprehensive corporate health and employee benefits package.
To compare database jobs and clinical trials data workflows with healthcare IT operations, check our analysis on Healthcare IT vs Clinical Healthcare.
🌟 Why Join Bristol Myers Squibb?
- BMS is a leading global biopharmaceutical company dedicated to building life-saving drugs.
- Provides a highly collaborative work culture with modern, advanced data tools like Veeva Vault and SAP.
- Clear career pathways from operations to study management and regulatory affairs.
📑 Resume Tips for BMS Clinical Operations Roles
- Highlight your specific experience in eTMF, CTMS, and Veeva databases.
- Detail your role in document QC, CSR compilation, or submission timeline tracking.
- Keep your resume layout clean, organized with headers, and ATS-friendly.
🎯 BMS Clinical Trial Support Specialist Interview Questions
- What is the difference between a CTMS and an eTMF system, and how do they interact?
- What does "Submission Ready Compliant" (SRC) mean when preparing clinical study documents?
- Explain your experience in compiling and reconciliating CSR appendices.
- How do you prioritize multiple document submissions with tight regulatory deadlines?
- Describe a situation where you identified a data discrepancy between databases and how you resolved it.
To learn more about clinical research coordinators and trial management operations, check our comprehensive Clinical Research Coordinator (CRC) Guide.
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through Bristol Myers Squibb's official Workday jobs portal using the link below. For step-by-step guidance on setting up your online application profile, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. Who is eligible to apply?
Graduates from B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Clinical Research, Biomedical Sciences, or Nursing fields with relevant clinical research experience.
Q. What is the work model for this role?
This is a full-time position located in Hyderabad, under a hybrid (Site-by-Design) model.
Q. What platforms will the specialist work on?
The specialist will primarily use Veeva Vault (eTMF/CTMS) and SAP systems.
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