Bristol Myers Squibb is Hiring a Clinical Trial Manager!

Location: Field-Based – United States (Hybrid)
Schedule: Full Time
Employment Type: Regular
Pay Range: $103,560 – $125,495 per year

Overview

Join Bristol Myers Squibb (BMS) and be part of a global biopharmaceutical leader transforming patients’ lives through science. As a Clinical Trial Manager (CTM), you’ll oversee clinical study operations at the country level — ensuring each trial meets timelines, budget, and quality standards.

This role is ideal for experienced clinical research professionals who thrive in complex, cross-functional environments. You’ll serve as the key point of contact between global study teams and local site operations, ensuring that every study milestone is achieved with excellence.

At BMS, you’ll be part of uniquely interesting work that’s challenging, meaningful, and life-changing.

Responsibilities

• Act as the primary contact for global and local study teams, vendors, and investigators.

• Lead and coordinate country-level clinical operations, ensuring compliance with GCP, ICH, and regulatory standards.

• Plan and manage study startup activities, site feasibility, and patient recruitment strategies.

• Oversee site monitoring, data quality, issue resolution, and inspection readiness.

• Ensure accurate documentation in CTMS, eDC, and eTMF systems.

• Participate in investigator meetings and coordinate database lock activities.

• Support regulatory and ethics submissions, amendments, and approvals.

• Drive CAPA implementation, risk management, and process improvements.

• Mentor peers and provide expertise in systems, therapeutic areas, and best practices.

Requirements

• Bachelor’s or Master’s degree in Life Sciences or a related field.

• Minimum 4 years of industry-related experience in clinical operations or trial management.

• Strong understanding of GCP, ICH, and regulatory frameworks.

• Proficiency in Microsoft Suite, CTMS, eDC, and eTMF systems.

• Excellent communication, organizational, and leadership skills.

• Ability to manage multiple projects and competing priorities effectively.

• Occasional local travel required (<1 month per quarter).

Preferred Qualifications

• Experience as a Subject Matter Expert (SME) in therapeutic areas, systems, or processes.

• Prior mentorship or training responsibilities in cross-functional teams.

• Familiarity with evolving country-level clinical research regulations.

Benefits

• Medical, Dental, and Vision Insurance

• 401(k) with Company Match and Financial Well-being Programs

• Paid Vacation, Sick Leave, and Holidays (including Global Shutdown Days)

• Parental Leave, Adoption, and Family Care Benefits

• Employee Assistance and Wellness Programs

• Tuition Reimbursement and Career Development Support

• Stock and Incentive Opportunities

• Hybrid Work Flexibility and Ergonomic Home Office Support