Bristol Myers Squibb (BMS) is hiring for a Clinical Trial Support Specialist position in Hyderabad, Telangana. The role is part of the company’s clinical development operations and involves supporting clinical trial submissions, document management, site setup, regulatory information, and clinical trial systems.
The position is offered on a full-time basis and requires professionals with a background in life sciences and relevant pharmaceutical, biotechnology, CRO, or clinical drug development experience.
The role involves close coordination with Submission Managers, outsourced partners, protocol and program teams, and multifunctional stakeholders across the oncology portfolio.
BMS Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Bristol Myers Squibb |
| Position | Clinical Trial Support Specialist |
| Job Location | Hyderabad, Telangana |
| Employment Type | Full Time |
| Job Requisition ID | R1606882 |
| Qualification | Bachelor’s Degree in Life Sciences |
| Experience | Approximately 4 Years Pharmaceutical/Biotech Experience |
| Relevant Clinical Experience | At least 2 Years in Pharma, Biotech or CRO Environment |
| Functional Area | Clinical Trials / Clinical Development |
| Therapeutic Area | Oncology Portfolio |
| Work Model | As assigned by BMS |
| Salary/CTC | Not Disclosed |
About Bristol Myers Squibb
Bristol Myers Squibb is a global biopharmaceutical company focused on developing medicines for serious diseases.
The Clinical Trial Support Specialist role supports operational activities associated with clinical trials, including preparation of submission documents, maintenance of clinical trial information, document management, site setup, regulatory milestones, and clinical trial technology systems.
Clinical Trial Support Specialist Job Description
The Clinical Trial Support Specialist will work with Submission Managers and other clinical development stakeholders to support the end-to-end management of clinical trial documents and submission activities.
The role requires strong organizational, analytical, communication, and project management capabilities. The selected candidate will also work with clinical trial systems such as Veeva Vault eTMF/CTMS and other technology platforms used to support clinical development.
Clinical Trial Submission and Documentation
Key responsibilities include:
- Support the end-to-end process for clinical trial documents and submissions.
- Prepare clinical trial submission documents in accordance with applicable regulatory requirements.
- Coordinate with Submission Managers on document creation and submission timelines.
- Support preparation of CSR appendices and Financial Disclosure Tables.
- Prepare related regulatory and clinical submission documents.
- Ensure documents are appropriately formatted.
- Check documents to ensure they meet Submission Ready Compliant (SRC) requirements.
- Follow applicable BMS procedures and document management requirements.
- Work with document templates and systems such as Core Template.
Clinical Trial Site and Regulatory Data Management
The role also involves maintaining important clinical trial information.
Responsibilities include:
- Coordinate with outsourced partners to create site numbers for new and ongoing clinical trials.
- Enter site milestones and regulatory approval dates.
- Maintain accurate trial information.
- Monitor the quality and completeness of assigned trial data.
- Ensure drug shipment addresses are entered accurately.
- Support the flow of shipment address information to SAP for investigational product supply to clinical sites.
Veeva and Clinical Trial Systems
The selected candidate will work with clinical trial technology and document management systems.
Key activities include:
- Reconcile Veeva information to maintain accurate clinical trial data.
- Work with Veeva Vault eTMF and CTMS where applicable.
- Support document management activities.
- Use clinical trial enabling technologies and databases.
- Work with MS Office and SharePoint.
- Maintain accurate information across relevant clinical systems.
Experience with Veeva Vault Clinical is preferred.
Regulatory and Compliance Responsibilities
The position requires knowledge of clinical research regulations and industry standards.
Candidates should understand:
- ICH guidelines
- Good Clinical Practice (GCP)
- Pharmaceutical regulatory requirements
- Clinical trial submission requirements
- Clinical drug development processes
- Protocol-related documentation
- Regulatory and operational requirements
The role requires assessing operational feasibility in the context of applicable GCP, ICH, and regulatory requirements.
Project Management and Problem Solving
The Clinical Trial Support Specialist will also contribute to efficient project execution.
Responsibilities include:
- Identify operational problems proactively.
- Apply critical thinking to complex issues.
- Develop mitigation and resolution approaches.
- Respond to assigned action items within required timelines.
- Manage multiple priorities.
- Assess risks associated with assigned activities.
- Escalate issues when appropriate.
- Support process improvement initiatives.
- Adapt to changing business and project requirements.
Cross-Functional Collaboration
The position involves interaction with multiple stakeholders across the clinical development organization.
The selected candidate may collaborate with:
- Submission Managers
- Protocol teams
- Program teams
- Clinical development teams
- Regulatory stakeholders
- Outsourced service providers
- Multifunctional teams
- Oncology portfolio stakeholders
The role requires the ability to work effectively within a global, multicultural, matrix environment.
Educational Qualification
The basic educational requirement is:
- Bachelor’s degree in Life Sciences
An advanced degree is considered an advantage.
Experience Requirements
The vacancy indicates:
- Approximately 4 years of pharmaceutical or biotechnology experience in a clinical drug development environment.
- At least 2 years of experience in a pharmaceutical, biotechnology, or CRO organization.
Relevant experience in clinical trial operations, submission support, clinical documentation, or clinical development can be applicable.
Required Skills and Competencies
Candidates should demonstrate:
- Knowledge of pharmaceutical clinical development
- Understanding of GCP and ICH requirements
- Knowledge of regulatory guidelines
- Clinical trial document management
- Strong organizational skills
- Time-management ability
- Analytical thinking
- Decision-making skills
- Risk assessment
- Problem-solving ability
- Project management skills
- Strong written communication
- Strong verbal communication
- Ability to manage multiple priorities
- Ability to work independently
- Cross-functional collaboration
- Adaptability in changing environments
- Ability to work effectively within a matrix organization
Technology and System Knowledge
Experience with the following technologies is beneficial:
- Veeva Vault Clinical
- Veeva Vault eTMF
- Veeva CTMS
- Clinical Trial Master File systems
- Microsoft Office
- SharePoint
- Clinical trial databases
- Clinical trial portals
- Other clinical development technology platforms
Understanding of Drug Development
Candidates should have a broad understanding of the different components of global pharmaceutical development, including:
- Non-clinical development
- Clinical development
- Safety
- Efficacy
- Labeling
- Regulatory requirements
- Business considerations
- Ethical requirements
- Product lifecycle activities
The role may require understanding how these factors influence clinical trial and program activities.
Work Location and Work Model
The position is based in Hyderabad, Telangana, India.
The posting explains that BMS uses different work models depending on the responsibilities of each position. The specific assigned model should be confirmed through the official job posting and recruitment process.
Salary / CTC
The salary or CTC for the Hyderabad Clinical Trial Support Specialist position has not been disclosed in the available vacancy details.
Candidates should confirm the compensation package and employment terms during the recruitment process.
Selection Process
The source vacancy does not provide a detailed selection process.
Candidates should refer to BMS recruitment communication for information regarding screening, interviews, assessments, or other hiring stages.
How to Apply
Interested and eligible candidates can apply through the official Bristol Myers Squibb careers page.
Candidates should highlight relevant experience in clinical trials, clinical development, regulatory submissions, Veeva systems, eTMF/CTMS, clinical documentation, GCP, ICH, and pharmaceutical/biotech operations in their resume.
Important Details Before Applying
- Position: Clinical Trial Support Specialist
- Company: Bristol Myers Squibb
- Location: Hyderabad, Telangana
- Employment: Full Time
- Requisition ID: R1606882
- Minimum qualification: Bachelor’s degree in Life Sciences
- Approximately 4 years of pharmaceutical/biotech experience is specified.
- At least 2 years should be in a pharmaceutical, biotech, or CRO environment.
- Experience with clinical trial systems is important.
- Veeva Vault Clinical experience is preferred.
- Knowledge of ICH and GCP is required.
- Strong organizational and project management skills are expected.
- The role supports clinical trial activities within the oncology portfolio.
- Salary/CTC has not been disclosed.
Frequently Asked Questions
1. What position is BMS hiring for?
Bristol Myers Squibb is hiring for a Clinical Trial Support Specialist position.
2. Where is the job located?
The position is based in Hyderabad, Telangana, India.
3. What qualification is required?
A Bachelor’s degree in Life Sciences is specified as the minimum educational qualification.
4. How much experience is required?
The vacancy specifies approximately 4 years of pharmaceutical or biotechnology experience in a clinical drug development setting, with at least 2 years in a pharmaceutical, biotech, or CRO environment.
5. Is Veeva experience required?
Experience with clinical trial master file systems or equivalent is expected, while Veeva Vault Clinical experience is specifically preferred.
6. What clinical systems are relevant to the role?
The position involves systems such as Veeva Vault eTMF, Veeva CTMS, clinical trial databases, portals, SharePoint, and other clinical trial technologies.
7. What regulatory knowledge is required?
Candidates should understand ICH, GCP, applicable regulatory guidelines, and the global pharmaceutical drug development process.
8. Does the role involve clinical trial submissions?
Yes. The position supports preparation, formatting, quality checking, maintenance, and submission-related activities for clinical trial documents.
9. Does the role involve oncology?
Yes. The job description specifically refers to interaction with multifunctional teams across the oncology portfolio.
10. What is the salary for this position?
The salary or CTC has not been disclosed in the available job posting.
Important Note
Job responsibilities, eligibility requirements, work model, compensation, and recruitment conditions may change during the hiring process. Candidates should verify the latest information on the official BMS Careers page before applying.