Bristol Myers Squibb (BMS) is a global biopharmaceutical leader committed to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a mission to transform patients’ lives through science, BMS fosters a culture of passion, innovation, and inclusion. Employees at BMS engage in meaningful work that drives advancements in healthcare, from optimizing production lines to pioneering breakthroughs in cell therapy.
BMS offers a dynamic work environment with competitive benefits, career growth opportunities, and a commitment to work-life balance. The company values diversity and encourages employees to push boundaries in their careers.
Job Openings at BMS Hyderabad
1. Real-World Data Analyst I
Job Requisition ID: R1589796
Job Description:
The Real-World Data (RWD) Analyst will play a crucial role in analyzing real-world healthcare data to generate insights that support clinical research, market access, and regulatory decision-making. This position involves working with large datasets from electronic health records (EHRs), claims databases, and registries to improve patient outcomes.
Key Responsibilities:
- Collaborate with researchers, clinicians, and market access teams to define data needs.
- Clean, preprocess, and analyze real-world data (RWD) for quality and consistency.
- Apply statistical techniques (propensity score matching, survival analysis, regression models) to derive insights.
- Conduct observational studies, comparative effectiveness research (CER), and patient outcomes analysis.
- Develop data analysis plans and interpret findings through reports and visualizations.
- Ensure compliance with regulatory requirements for RWD analysis.
Skills & Qualifications:
- Bachelor’s/Master’s in Biostatistics, Epidemiology, Health Informatics, or related field.
- 2-3 years of experience in real-world data analysis (pharma/healthcare preferred).
- Proficiency in R, SAS, SQL; familiarity with Tableau/Power BI is a plus.
- Strong analytical, problem-solving, and communication skills.
2. eTMF Specialist
Job Requisition ID: R1587048
Job Description:
The eTMF (Electronic Trial Master File) Specialist ensures proper documentation management for BMS clinical trials. This role involves uploading, reviewing, and maintaining trial-related documents in compliance with regulatory standards.
Key Responsibilities:
- Upload and quality-check clinical trial documents in the eTMF system.
- Ensure documents meet ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate).
- Collaborate with study teams to manage document completeness and compliance.
- Track essential records and resolve discrepancies in documentation.
- Support clinical trials from start-up to close-out phases.
Skills & Qualifications:
- Bachelor’s degree in Life Sciences, Business Administration, or related field.
- 1-2 years of experience in clinical trial documentation management.
- Knowledge of ICH/GCP guidelines and experience with Veeva Vault Clinical preferred.
- Strong organizational, communication, and stakeholder management skills.
3. Clinical Trial Support Specialist
Job Description
The Clinical Trial Support Specialist plays a key role in ensuring efficient clinical trial documentation, submissions, and compliance with regulatory standards. This position involves collaborating with Submission Managers, regulatory teams, and outsourcing partners to streamline trial processes and maintain accurate records.
Key Responsibilities
✔ Document Preparation & Compliance:
- Prepare Clinical Trial Submission documents (CSR appendices, Financial Disclosure Tables, etc.) in line with ICH/GCP guidelines.
- Ensure documents are Submission Ready Compliant (SRC) and properly formatted.
✔ Trial Management & Data Accuracy:
- Assign site numbers for new and ongoing trials.
- Track regulatory approval dates and maintain trial health records.
- Ensure accurate drug shipment addresses for Investigational Product (IP) supply.
✔ System & Process Optimization:
- Perform Veeva (eTMF/CTMS) reconciliations to ensure data accuracy.
- Utilize MS Office, SharePoint, and Veeva Vault Clinical for document management.
- Identify process improvements and mitigate risks proactively.
✔ Cross-Functional Collaboration:
- Work with senior-level teams (Oncology, Regulatory, Clinical Operations).
- Support global drug development processes with compliance expertise.
Skills & Qualifications
✅ Education: Bachelor’s degree in Life Sciences, Pharmacy, or related field.
✅ Experience: 2-4 years in clinical trial documentation, regulatory submissions, or clinical operations.
✅ Technical Skills:
- Proficiency in Veeva Vault Clinical, CTMS, MS Office, SharePoint.
- Knowledge of eTMF, ICH/GCP, and clinical trial regulations.
✅ Soft Skills: - Strong project management, problem-solving, and analytical skills.
- Ability to collaborate with global teams and manage multiple priorities.
Why Join Bristol Myers Squibb?
🔹 Impactful Work: Contribute to life-saving therapies and patient-centric research.
🔹 Career Growth: Opportunities for professional development in a global biopharma leader.
🔹 Inclusive Culture: Work with diverse, high-performing teams.
🔹 Hybrid Work Options: Flexible arrangements for eligible roles.
How to Apply
Application Link for Real World Data Analyst I
Application Link for eTMF Specialist
Application Link for Clinical Trial Support Specialist
