Bristol Myers Squibb Hiring Clinical Research Associate

Bristol Myers Squibb Hiring Clinical Research Associate | CRA Jobs in Mumbai for Life Sciences Professionals

Bristol Myers Squibb (BMS) is hiring for Clinical Research Associate (CRA) roles in Mumbai under its Clinical Research and Development division. This is a full-time opportunity for candidates with 2–3 years of clinical research experience, offering exposure to global clinical trials, regulatory compliance, and advanced drug development processes. The role plays a critical part in ensuring patient safety, data integrity, and successful execution of clinical studies.

Company Overview

Bristol Myers Squibb is a globally recognized biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for serious diseases. With strong expertise in oncology, immunology, cardiovascular, and cell therapy, BMS is known for transforming patient outcomes through cutting-edge research and clinical innovation.

The company collaborates with global clinical sites, regulatory authorities, and research partners to accelerate drug development and bring life-saving therapies to market. Working at BMS provides professionals with exposure to high-impact clinical trials, global regulatory frameworks, and a culture focused on scientific excellence and patient-centric innovation.

Job Role & Responsibilities

As a Clinical Research Associate (CRA), you will act as the primary point of contact for clinical trial sites, ensuring compliance, monitoring, and quality execution of studies.

• Conduct site qualification, initiation, monitoring, and close-out visits
• Ensure compliance with ICH-GCP guidelines, SOPs, and regulatory requirements
• Verify clinical data accuracy, completeness, and integrity (ALCOA principles)
• Monitor site performance, patient safety, and protocol adherence
• Prepare monitoring reports and maintain documentation
• Support audit and inspection readiness for regulatory authorities
• Build relationships with investigators, sites, and cross-functional teams
• Analyze site metrics and identify risks, implementing mitigation strategies
• Support site selection, feasibility assessments, and regulatory submissions
• Manage clinical systems such as CTMS, eTMF, and EDC platforms
• Oversee investigational product (IMP) handling and documentation

This role is essential in ensuring successful clinical trial delivery, regulatory compliance, and advancement of new therapies in the healthcare ecosystem.

Eligibility / Qualifications

Candidates must meet the following criteria:

• Bachelor’s degree in Life Sciences, Pharmacy, or related field
• 2–3 years of experience as a Clinical Research Associate or similar role

Relevant courses include: B.Pharmacy, M.Pharmacy, BSc Life Sciences, MSc Clinical Research, MSc Biotechnology, Pharm.D, Life Sciences

Key skills required:

• Strong understanding of clinical trial processes and ICH-GCP guidelines
• Experience in site monitoring and clinical operations
• Knowledge of regulatory requirements and audit processes
• Proficiency in CTMS, eTMF, and EDC systems
• Analytical thinking and problem-solving ability
• Strong communication and stakeholder management skills

Location & Salary

• Location: Mumbai, Maharashtra
• Work Mode: On-site / Hybrid (as per project requirements)
• Salary: Approximately ₹10 LPA – ₹18 LPA (based on industry benchmarks for CRA roles in India)

Application Process

Interested candidates can apply through the official BMS careers portal:

Apply Here: https://jobs.bms.com/careers/job/137480624971

Ensure your resume highlights your clinical trial monitoring experience, regulatory knowledge, and hands-on exposure to clinical systems to improve your chances of selection.

Frequently Asked Questions (FAQs)

1. What experience is required for this role?
Candidates need 2–3 years of clinical research experience.

2. What is the main responsibility of a CRA?
The role focuses on site monitoring, regulatory compliance, and clinical trial execution.

3. What qualifications are required?
A degree in Life Sciences or Pharmacy is required.

4. Is travel required in this role?
Yes, site visits and monitoring activities may require travel.

5. What systems will I work on?
You will use CTMS, eTMF, and EDC systems for clinical trial management.

Summary Table

Company	Bristol Myers Squibb
Vacancies	Clinical Research Associate (CRA)
Required Education	B.Pharmacy, M.Pharmacy, BSc Life Sciences, MSc Clinical Research, MSc Biotechnology, Pharm.D
Experience	2–3 Years

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