Are you searching for the latest Clinical Research Jobs in Hyderabad? Here’s an exciting opportunity to join one of the world’s leading biopharmaceutical companies. Bristol Myers Squibb (BMS) is hiring a Clinical Trial Support Specialist for its Hyderabad office. If you have a passion for clinical operations, regulatory documentation, and supporting global clinical trials, this role could be the perfect next step in your career.

Whether you’re an experienced professional or looking to strengthen your expertise in clinical trial support, this position offers exposure to international clinical development projects, industry-leading systems, and excellent career advancement opportunities.

📌 Job Overview

🏢 Company: Bristol Myers Squibb (BMS)

💼 Position: Clinical Trial Support Specialist

📍 Location: Hyderabad, Telangana, India

🕒 Job Type: Full-Time

🏠 Work Mode: On-site / Hybrid (Subject to company policy)

📅 Job Category: Clinical Research | Clinical Operations | Regulatory Documentation

🌍 About Bristol Myers Squibb

Bristol Myers Squibb is a globally recognized pharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that improve patients’ lives. With operations across multiple countries, the company focuses on advancing treatments in oncology, hematology, cardiovascular diseases, immunology, neuroscience, and other therapeutic areas.

Employees at BMS work in a collaborative, science-driven environment where innovation, integrity, and patient care remain at the core of every project.

Working at Bristol Myers Squibb provides professionals with opportunities to collaborate with global teams, gain exposure to advanced technologies, and contribute to meaningful healthcare advancements.

🔬 About the Clinical Trial Support Specialist Role

Clinical trials generate a significant amount of documentation that must meet strict regulatory standards. The Clinical Trial Support Specialist ensures that these records are accurate, complete, and compliant throughout the study lifecycle.

The selected candidate will support clinical submission activities, coordinate documentation, maintain trial management systems, and collaborate with multiple stakeholders to ensure smooth execution of global clinical research projects.

This role combines clinical operations, documentation management, regulatory compliance, and project coordination, making it an excellent opportunity for professionals interested in long-term careers within clinical research.

🎯 Key Responsibilities

As a Clinical Trial Support Specialist, your responsibilities may include:

Preparing and organizing clinical trial documentation for regulatory submissions.
Ensuring all required documents are accurate, complete, and submission-ready.
Supporting submission managers with document preparation and coordination.
Assisting in the creation of Clinical Study Report (CSR) appendices.
Managing site numbering for ongoing and new clinical studies.
Updating clinical trial milestones and regulatory approval information.
Maintaining investigational drug shipment records.
Performing reconciliation activities between Veeva eTMF and CTMS platforms.
Identifying documentation discrepancies and resolving operational issues.
Coordinating with internal departments and external stakeholders.
Following company SOPs, ICH-GCP guidelines, and regulatory standards.
Supporting additional clinical operations activities whenever required.

🎓 Educational Qualification

Candidates from the following educational backgrounds are encouraged to apply:

B.Pharm
M.Pharm
Pharm.D
B.Sc Life Sciences
M.Sc Life Sciences
Biotechnology
Microbiology
Biochemistry
Clinical Research
Biomedical Sciences
Other relevant Life Science disciplines

Relevant industry experience in clinical operations or trial documentation will be an added advantage.

💼 Required Skills

The ideal candidate should possess:

Excellent organizational skills
Strong documentation abilities
High attention to detail
Analytical thinking
Time management skills
Effective communication
Ability to manage multiple priorities
Problem-solving mindset
Team collaboration
Adaptability in a fast-paced environment

📚 Preferred Knowledge

Candidates familiar with the following areas may have an advantage:

Clinical Trial Documentation
Good Clinical Practice (GCP)
ICH Guidelines
Regulatory Submission Processes
Clinical Trial Management Systems (CTMS)
Electronic Trial Master File (eTMF)
Veeva Vault
Clinical Study Reports
Drug Development Lifecycle
Clinical Operations
Quality Documentation
Regulatory Compliance

🌟 Why Join Bristol Myers Squibb?

Working at Bristol Myers Squibb offers numerous professional benefits:

✅ Global exposure to clinical development projects

✅ Opportunity to work with experienced clinical research professionals

✅ Continuous learning and development programs

✅ Collaborative and inclusive work culture

✅ Exposure to modern clinical technologies

✅ Career advancement opportunities

✅ Stable and respected pharmaceutical organization

✅ Work that contributes directly to improving patient health worldwide

🚀 Career Growth Opportunities

Experience gained in this position can help professionals advance into roles such as:

Clinical Trial Associate (CTA)
Clinical Operations Associate
Clinical Project Coordinator
Clinical Operations Specialist
Regulatory Operations Specialist
Clinical Trial Manager
Clinical Project Manager
Global Clinical Operations Lead
Study Start-Up Specialist
Clinical Documentation Manager

The skills acquired in this role are highly valued across pharmaceutical companies, CROs, and biotechnology organizations.

📝 Resume Tips Before Applying

To improve your chances of getting shortlisted:

Update your resume with your latest educational qualifications and work experience.
Highlight any experience in Clinical Research or Clinical Operations.
Mention familiarity with GCP, ICH Guidelines, CTMS, or eTMF systems.
Showcase documentation management and project coordination experience.
Include certifications related to Clinical Research if applicable.
Carefully align your resume with the responsibilities mentioned in the job description.

👩‍🔬 Who Should Apply?

This opportunity is suitable for candidates interested in:

Clinical Research Jobs
Clinical Operations Careers
Regulatory Affairs
Trial Documentation
Clinical Trial Management
Drug Development
Pharmaceutical Industry
Biotechnology Careers
Life Sciences Jobs
Global Clinical Studies

Fresh graduates with relevant internships and experienced professionals looking to grow within clinical research are encouraged to explore this opportunity.

📢 Why This Role Matters

Clinical trials are essential for developing safe and effective medicines. Every successful study depends on accurate documentation, regulatory compliance, and seamless coordination between multiple teams.

As a Clinical Trial Support Specialist, you become an important part of this process by ensuring that critical study documentation is maintained according to global standards. Your work directly supports the successful execution of clinical research programs that can improve patient outcomes worldwide.

📌 How to Apply?

Interested candidates can apply directly through the official Bristol Myers Squibb careers portal.

👉 Apply Now

https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Hyderabad—TS—IN/Clinical-Trial-Support-Specialist_R1602785

Note: Please apply only through the official company website. Ensure your resume is updated before submitting your application.

⚠️ Disclaimer

Jobs On The Way shares job opportunities for informational and educational purposes only. We are not a recruitment agency and do not charge any fee for job applications. Recruitment decisions are made solely by the hiring organization. Candidates are advised to verify all job details on the official company careers page before applying.

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Bristol Myers Squibb Clinical Trial Support Specialist Jobs

Bristol Myers Squibb Hiring Clinical Trial Support Specialist in Hyderabad | Apply Now | Clinical Research Jobs 2026