Apply for Clinical Research Associate Job at Bristol Myers Squibb, Mumbai. 2–3 years experience required. Life Sciences graduates preferred.
Company: Bristol Myers Squibb (BMS)
Job Title: Clinical Research Associate (CRA)
Location: Mumbai, Maharashtra, India
Employment Type: Full-Time
Experience Required: 2–3 Years
Education Qualification: Bachelor’s Degree in Life Sciences or equivalent field
Job Requisition ID: R1596192
Application Mode: Online
About Bristol Myers Squibb
Bristol Myers Squibb (BMS) is one of the world’s leading biopharmaceutical companies, driven by the powerful mission of “Transforming patients’ lives through science™.” The organization is recognized globally for its pioneering research in oncology, immunology, cardiovascular, and hematology, and for introducing innovative therapies that redefine the standards of patient care. Clinical Research Associate Job at Bristol Myers Squibb
At BMS, employees are not just part of a company — they are part of a community of innovators, scientists, and healthcare professionals who are committed to improving health outcomes across the world. The company offers a dynamic and inclusive work culture where your contributions matter and your career can reach new heights. Clinical Research Associate Job at Bristol Myers Squibb
Working at BMS means working on challenging, meaningful, and life-changing projects every single day. Whether you are in research, operations, or data management, your work helps improve the lives of patients globally. Clinical Research Associate Job at Bristol Myers Squibb
Position Summary
Bristol Myers Squibb is seeking an experienced and dedicated Clinical Research Associate (CRA) to join its Mumbai team.
As a Clinical Research Associate, you will serve as the primary point of contact at the site level for both internal and external stakeholders. You will be responsible for ensuring the quality, integrity, and regulatory compliance of clinical trial sites. This includes monitoring the conduct of clinical trials according to the study protocol, company Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) guidelines, and Good Clinical Practice (GCP) standards.
This role is ideal for professionals passionate about clinical research, data accuracy, patient safety, and compliance with global standards. Clinical Research Associate Job at Bristol Myers Squibb
Key Responsibilities
The Clinical Research Associate will perform a wide range of duties focused on clinical site management, documentation, compliance, and collaboration. Clinical Research Associate Job at Bristol Myers Squibb
1. Clinical Site Monitoring
- Conduct site qualification, initiation, monitoring, and close-out visits across all phases of clinical trials.
- Ensure that all trial activities comply with the Site Monitoring Plan, study protocol, and ICH-GCP guidelines.
- Verify the accuracy, completeness, and integrity of clinical data captured at the site level.
2. Data Verification and Documentation
- Review electronic and paper records to validate clinical data accuracy.
- Ensure data reliability by following ALCOA principles (Attributable, Legible, Contemporaneous, Original, and Accurate).
- Support site staff with documentation training and compliance audits.
3. Compliance and Quality Oversight
- Monitor adherence to ethical, scientific, and regulatory standards.
- Participate in sponsor and health authority audits as required.
- Develop and implement corrective and preventive actions (CAPA) following audit findings.
4. Stakeholder and Site Relationship Management
- Build and maintain professional relationships with investigators, site staff, vendors, and cross-functional teams.
- Act as the company’s representative during all site interactions.
- Motivate and influence clinical sites to meet recruitment, retention, and data submission goals.
5. Risk Management and Issue Resolution
- Identify and assess risks at the site and study levels.
- Proactively develop and execute mitigation strategies.
- Adjust monitoring approaches based on real-time data trends and performance indicators.
6. Data Review and Analytical Evaluation
- Analyze operational metrics and site performance data.
- Adjust monitoring plans using centralized, remote, and risk-based monitoring approaches.
- Collaborate with project managers and clinical leads to optimize study timelines and data quality.
7. Regulatory and Drug Accountability
- Oversee investigational product management, including labeling, reconciliation, and documentation.
- Support site staff with Ethics Committee submissions and informed consent form (ICF) reviews.
8. Technology and Systems Utilization
- Efficiently use BMS systems such as CTMS, eTMF, RBQM dashboards, and EDC systems.
- Maintain up-to-date and accurate records of site monitoring activities.
Required Qualifications
- Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field.
- Experience: 2–3 years of relevant experience in clinical research, preferably as a Clinical Research Associate.
- Preferred: Experience with pharmaceutical or biotech sponsors and familiarity with the drug development process.
- License: A valid driver’s license, as local travel may be required.
Skills and Core Competencies
BMS seeks professionals who combine scientific expertise with integrity, adaptability, and analytical thinking. Clinical Research Associate Job at Bristol Myers Squibb
Technical and Regulatory Knowledge
- In-depth understanding of clinical research methodologies and regulatory frameworks.
- Working knowledge of ICH-GCP, local regulations, and ethical guidelines.
- Strong grasp of the drug development lifecycle and clinical data management systems.
Analytical and Problem-Solving Skills
- Ability to assess clinical site data, detect inconsistencies, and implement effective solutions.
- Experience using data visualization or risk-based monitoring tools to drive decisions.
Communication and Relationship Building
- Excellent written and verbal communication in English (and local language, if required).
- Ability to build strong relationships with investigators, clinical teams, and regulatory bodies.
- Skilled at managing multiple studies and prioritizing under tight deadlines.
Adaptability and Growth Mindset
- Openness to learning new technologies and evolving methodologies.
- Proactive approach to professional development and self-improvement.
Software Proficiency
- Microsoft Office Suite
- Clinical Trial Management Systems (CTMS)
- Electronic Data Capture (eDC) Systems
- Electronic Trial Master File (eTMF)
- Risk-Based Monitoring (RBM) tools such as Veeva, Medidata, and CluePoints
Work Environment and On-Site Protocol
Bristol Myers Squibb follows a structured workplace model to support productivity, collaboration, and flexibility. Clinical Research Associate Job at Bristol Myers Squibb
- Site-Essential Roles: Require 100% on-site presence.
- Site-by-Design Roles: Hybrid model with at least 50% on-site work.
- Field-Based or Remote Roles: Require travel for monitoring and stakeholder meetings.
For this CRA role, on-site presence and field travel are essential to oversee study sites and ensure clinical data compliance.
Employee Benefits and Work-Life Balance
BMS believes that employees perform best when their professional and personal goals are balanced. The company offers: Clinical Research Associate Job at Bristol Myers Squibb
- Competitive salary and performance-based bonuses.
- Health, dental, and vision insurance plans.
- Flexible work options and paid time off.
- Employee training and development programs.
- Inclusive and diverse workplace culture that values innovation and integrity.
Bristol Myers Squibb is also committed to diversity, accessibility, and disability inclusion. The company provides reasonable accommodations to support employees and applicants during the recruitment process and beyond. Clinical Research Associate Job at Bristol Myers Squibb
Why Work at Bristol Myers Squibb
At BMS, you’re not just joining a company — you’re joining a purpose-driven global team committed to advancing science and improving patient outcomes. Every project is backed by collaboration, innovation, and compassion. Clinical Research Associate Job at Bristol Myers Squibb
By joining as a Clinical Research Associate, you’ll gain:
- Exposure to cutting-edge clinical research projects.
- Direct collaboration with leading investigators and healthcare institutions.
- Opportunities to contribute to global clinical development programs.
- A workplace that fosters professional growth, ethical practice, and scientific excellence.
If you are ready to take your clinical research career to the next level, BMS offers the perfect platform to do so. Clinical Research Associate Job at Bristol Myers Squibb
How to Apply
Interested candidates are encouraged to apply through the official Bristol Myers Squibb careers portal:
👉 https://careers.bms.com
If the Clinical Research Associate role aligns with your passion for clinical trials and data integrity — even if your experience doesn’t match every requirement — BMS encourages you to apply. You could be one step away from a career that transforms lives, including your own. Clinical Research Associate Job at Bristol Myers Squibb
Conclusion
The Clinical Research Associate position at Bristol Myers Squibb is an exceptional opportunity for professionals in clinical research who want to grow within a world-class biopharmaceutical organization. This role offers not only competitive compensation and global exposure but also the satisfaction of working on projects that genuinely impact patient health worldwide. Clinical Research Associate Job at Bristol Myers Squibb
Join BMS today and become part of a company where science meets purpose, and careers become life-changing.
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