Senior Manager, Global Clinical Scientist (Cell Therapy)

Job Overview

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Compensation

Salary
Range $150,770.00 - $210,110.00
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Benefits

health coverage
wellbeing support
Financial well-being and protection
Paid Time Off
401(k) Plan
Life insurance
Disability insurance

Job Description

Bristol Myers Squibb is a leading global biopharmaceutical company committed to transforming patients' lives through innovative science. With a rich heritage rooted in pharmaceutical excellence and cutting-edge research, the company strives every day to create meaningful advances in the treatment of serious diseases, including cancer, cardiovascular conditions, immunology, and cell therapy. Recognized for its culture of inclusion, collaboration, and integrity, Bristol Myers Squibb offers employees the opportunity to grow professionally and make a significant impact at a global scale. The company values balance and flexibility, providing comprehensive benefits and resources to support both career ambitions and personal well-being.

The Senior Manager, Global Clinical Scientist role at Bristol Myers Squibb embodies the spirit of innovation and dedication to patient care. This position is centered on providing scientific expertise essential to designing and executing clinical studies and programs that support the company’s groundbreaking therapeutic advances, particularly in cell therapy. The role involves close collaboration with cross-functional clinical teams to oversee clinical trial activities, ensuring scientific rigor and compliance with regulatory standards. As a potential Clinical Trial Lead, the Senior Manager will lead or support clinical trial execution, co-lead study team meetings, and work alongside external thought leaders and key opinion leaders to drive research outcomes that positively influence patient therapies globally.

The position requires a keen ability to develop and present protocol documents, informed consent forms, and amendments to governance and development committees. Responsibilities extend to conducting literature reviews, preparing clinical trial documentation, monitoring data trends, and contributing to regulatory submissions and clinical study reports. The Senior Manager will also develop training materials for study investigators and clinical research associates, ensuring high-quality execution of clinical trials.

Candidates for this role are expected to hold a degree in life sciences, with qualifications such as MD, PhD, PharmD, MS, or RN preferred, and possess foundational knowledge of Good Clinical Practice (GCP), the drug development process, study design, statistics, and clinical operations. This position requires a detail-oriented approach, critical thinking, and the ability to adapt to shifting priorities in a fast-paced industry. Intermediate skills in medical writing, project management, and Microsoft Office applications, along with clinical data review tools, are essential.

This full-time position offers competitive compensation ranging approximately from $150,770 to $210,110 annually, depending on location and experience, alongside opportunities for additional incentives such as cash bonuses and stock options. Bristol Myers Squibb’s commitment to well-being is reflected in extensive benefits, including medical, pharmacy, dental, and vision coverage; wellbeing support programs; financial protection plans; and generous paid time off policies. The role may require domestic and international travel, providing exposure to diverse clinical environments and global research collaboration.

By joining Bristol Myers Squibb as a Senior Manager, Global Clinical Scientist, candidates have the chance to advance careers through uniquely challenging and rewarding work environments that emphasize scientific innovation, teamwork, and life-changing outcomes for patients worldwide. This role is pivotal in delivering clinical evidence that helps shape the future of medicine, with robust support to ensure employee growth and work-life balance in a dynamic biopharmaceutical setting.

Job Requirements

  • Degree in life sciences such as MD, PhD, PharmD, MS, RN or other scientific field
  • basic knowledge of GCP/ICH and drug development process
  • ability to understand assigned protocol(s) and their requirements
  • basic knowledge supporting program-specific data review and trend identification
  • intermediate medical writing skills and medical terminology
  • basic planning and project management skills
  • detail-oriented with commitment to quality
  • basic knowledge of disease area, compound, current clinical landscape
  • basic knowledge of data monitoring committees and independent response adjudication committees
  • intermediate critical thinking and problem-solving skills
  • adaptable and flexible with ability to adjust to multiple demands and shifting priorities
  • intermediate skills in Microsoft Word, Excel, PowerPoint and data review tools
  • willingness to travel domestically and internationally

Job Qualifications

  • Degree in life sciences such as MD, PhD, PharmD, MS, RN or other scientific field
  • basic knowledge of GCP/ICH and drug development process
  • ability to understand clinical protocols and requirements
  • intermediate medical writing skills and medical terminology knowledge
  • basic planning and project management skills
  • basic knowledge of disease area and current clinical landscape
  • intermediate critical thinking and problem-solving skills
  • intermediate skills in Microsoft Word, Excel, PowerPoint and clinical data review tools

Job Duties

  • Collaborate and liaise with external partners such as key opinion leaders
  • seek out and enact best practices with instruction
  • provide regular and timely updates to management
  • develop protocol and informed consent form documents and amendments and present these to governance committees
  • conduct literature review
  • submit clinical documents to the trial master file
  • develop site and CRA training materials and present these at site initiation visits and investigator meetings
  • review clinical narratives
  • monitor clinical data for specific trends
  • develop Data Review Plan in collaboration with Data Management
  • ensure case report form design supports data collection in alignment with protocol
  • submit clinical contributions to clinical study reports and clinical portions of regulatory documents

Job Criteria

Experience

Mid Level (3-7 years)


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