WhatsApp Group Join Now
Telegram Group Join Now

Bristol Myers Squibb Hiring for Clinical Trial Manager


Bristol Myers Squibb Hiring for Clinical Trial Manager (CTM) in Mumbai. Apply online for full-time pharma clinical research jobs.


About Bristol Myers Squibb

Bristol Myers Squibb (BMS) is a global biopharmaceutical leader dedicated to transforming patients’ lives through science. With operations in over 60 countries, BMS combines cutting-edge innovation, patient-centric research, and a mission-driven approach to deliver breakthrough therapies in oncology, immunology, cardiovascular diseases, and hematology. Bristol Myers Squibb Hiring for Clinical Trial Manager

The company fosters a culture that values inclusion, collaboration, and excellence — ensuring employees grow personally and professionally while contributing to life-changing advancements in healthcare. Bristol Myers Squibb Hiring for Clinical Trial Manager

If you’re a professional looking for a challenging, meaningful, and rewarding career in clinical research, this opportunity as a Clinical Trial Manager (CTM) in Mumbai could be your next big step. Bristol Myers Squibb Hiring for Clinical Trial Manager


Job Overview – Clinical Trial Manager (CTM)

Position: Clinical Trial Manager (CTM)
Company: Bristol Myers Squibb (BMS)
Location: Mumbai, Maharashtra, India
Employment Type: Full-time
Experience: Minimum 4 years
Job ID: R1596303
Posted On: October 28, 2025

This full-time position offers an opportunity to join one of the world’s most respected pharmaceutical companies, where you’ll be responsible for managing end-to-end clinical trial operations at the country level. Bristol Myers Squibb Hiring for Clinical Trial Manager


Role Summary

The Clinical Trial Manager (CTM) plays a critical role in overseeing the operational aspects of clinical trials across India. The CTM ensures that all trials are executed efficiently, adhering to strict timelines, budgets, and quality standards. Bristol Myers Squibb Hiring for Clinical Trial Manager

The role demands effective coordination with both internal and external stakeholders, including investigators, vendors, and regulatory authorities. You will serve as the primary country-level point of contact for study operations and be accountable for operational excellence, compliance, and quality delivery. Bristol Myers Squibb Hiring for Clinical Trial Manager

READ THIS  Hetero Biopharma Hiring for Production

Key Responsibilities

As a Clinical Trial Manager at Bristol Myers Squibb, you will be responsible for managing and supervising various aspects of clinical research projects. Your primary duties include: Bristol Myers Squibb Hiring for Clinical Trial Manager

  1. Project Coordination and Oversight
    • Serve as the main point of contact for the country in communication with global study teams.
    • Coordinate local cross-functional teams to ensure study goals and timelines are achieved.
    • Implement the country and site feasibility process, validating study targets as endorsed by country leadership.
  2. Study Start-Up and Execution
    • Develop and execute study start-up timelines and activities in collaboration with the Global Trial Acceleration Centre (GTAC).
    • Lead country and site-level patient recruitment strategies and ensure enrollment targets are met.
    • Assess and manage local vendors during the study start-up period.
  3. Operational Management
    • Monitor and maintain data accuracy within the Clinical Trial Management System (CTMS).
    • Ensure complete documentation in the Electronic Trial Master File (eTMF) and manage country-level data integrity.
    • Validate study-related materials such as protocols, informed consent forms (ICFs), and patient information documents.
  4. Quality Assurance and Compliance
    • Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
    • Maintain readiness for inspections and audits.
    • Drive Corrective and Preventive Action (CAPA) processes and ensure timely implementation of audit findings.
  5. Stakeholder and Site Management
    • Build strong relationships with investigators, clinical sites, and vendors.
    • Coordinate site monitoring visits, investigator meetings, and issue resolution.
    • Act as a local point of contact for site-level queries and communications.
  6. Regulatory and Ethics Submissions
    • Prepare and submit documents to Health Authorities and Ethics Committees for protocol and amendment approvals.
    • Collaborate with the regulatory and central teams to coordinate responses to Ministry of Health queries.
  7. Reporting and Documentation
    • Maintain up-to-date records in CTMS, eDC, and eTMF systems.
    • Coordinate database locks and manage query follow-ups.
    • Support financial activities such as vendor invoice resolution and patient compensation claims.

Qualifications and Eligibility Criteria

Educational Qualification:

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or a related field.
READ THIS  Hetero Drugs Walk-In Drive for Quality Control Job

Experience:

  • Minimum 4 years of industry-related experience in clinical trial management or clinical research operations.
  • Experience leading or being part of cross-functional teams or global project initiatives.

Core Competencies Required:

  • Strong understanding of GCP, ICH Guidelines, and country-specific regulations.
  • Excellent knowledge of clinical research processes, data management, and quality systems.
  • Proven organizational, problem-solving, and decision-making skills.
  • Effective communication and leadership abilities to coordinate with stakeholders across multiple levels.
  • Proficiency in CTMS, eDC, eTMF, and Microsoft Office Suite.

Key Skills and Attributes

  • Exceptional planning and time management skills.
  • Ability to handle multiple priorities under tight deadlines.
  • Strong analytical mindset and attention to detail.
  • Commitment to quality, ethics, and compliance.
  • Ability to adapt to dynamic project requirements.
  • Fluency in English and local language preferred.

Software Proficiency

Candidates must be proficient in the following tools and platforms: Bristol Myers Squibb Hiring for Clinical Trial Manager

  • Microsoft Office Suite (Excel, Word, PowerPoint)
  • Clinical Trial Management Systems (CTMS)
  • Electronic Data Capture (eDC) systems
  • Electronic Trial Master File (eTMF)

Travel Requirements

  • Occasional local travel may be required (less than one month per quarter) for site visits, investigator meetings, or audits.

Work Environment and Benefits

Bristol Myers Squibb is known for its flexible and inclusive work environment. Depending on the nature of the role, employees may work: Bristol Myers Squibb Hiring for Clinical Trial Manager

  • On-site,
  • Hybrid (site-by-design), or
  • Field-based/Remote-by-design arrangements.

Employee Benefits Include:

  • Competitive salary and performance-based incentives.
  • Health, wellness, and insurance programs.
  • Professional development and global career growth opportunities.
  • Access to cutting-edge research and technology.
  • Supportive, collaborative, and inclusive company culture.

Equal Employment Opportunity

BMS is committed to providing equal employment opportunities to all qualified applicants. The company promotes a transparent recruitment process and provides reasonable workplace accommodations for individuals with disabilities. Bristol Myers Squibb Hiring for Clinical Trial Manager

READ THIS  USV Pharma Hiring for API Production Jobs

For accommodation requests, candidates can contact:
📧 adastaffingsupport@bms.com


Why Join Bristol Myers Squibb?

At Bristol Myers Squibb, every employee plays an essential role in achieving the company’s mission — Transforming patients’ lives through science.

As a Clinical Trial Manager, you will:

  • Be part of life-changing medical innovations.
  • Lead high-impact clinical trials that advance global healthcare.
  • Collaborate with world-class researchers and experts.
  • Grow your career in a dynamic, science-driven environment.

This is more than a job; it’s an opportunity to make a lasting difference in patients’ lives while building a rewarding career. Bristol Myers Squibb Hiring for Clinical Trial Manager


How to Apply

Interested and qualified candidates can apply online through the official Bristol Myers Squibb careers portal:

Ensure your application includes:

  • Updated Resume
  • Educational and Professional Certificates
  • Relevant Experience Details

Application Link


Important Notes

  • All applicants must comply with local COVID-19 guidelines.
  • The company encourages full vaccination and booster updates for all employees.
  • Applicants with prior arrests or convictions will be considered in compliance with local laws.
  • Personal data collected during the recruitment process will be handled in accordance with BMS privacy regulations.

Conclusion

The Clinical Trial Manager (CTM) position at Bristol Myers Squibb offers a rare opportunity to contribute to transformative healthcare research while developing a rewarding career in one of the world’s most reputable pharmaceutical organizations.

If you’re passionate about clinical research, regulatory compliance, and making a difference in patients’ lives, don’t miss this chance. Bristol Myers Squibb Hiring for Clinical Trial Manager

Apply now and take your first step toward a life-changing career at BMS.

For verified pharma job updates, visit PharmaJobHub.in  India’s trusted pharma career portal.

Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.


India's Trusted Pharma Job Website
for delivering Latest Genuine Pharma Job Updates.
WhatsApp Group Join Now
Telegram Group Join Now

Leave a Comment

×
WhatsApp Icon Fast Jobs Alert Join
Resume Icon Make Your Best Resume Start