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Clinical Trial Associate, Clinical Operations

Bristol Myers Squibb
Remote - United States, United States, United StatesRemotefull_timeVerifiedPosted 12 Sept 2025
💰 $85,756/yr($70,769/yr$85,756/yr)

About the role

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Summary

The Clinical Trials Associate (CTA) is an integral part of the study team and provides project system, tracking, and administrative support to the study team(s) through all phases of clinical study activities (feasibility, start-up, maintenance, and close-out) under the direction of the Head of Clinical Operations.

Job Responsibilities

Essential duties and responsibilities include the following.  Other duties may be assigned.

  • Work closely with the study execution team to provide project system, tracking and administrative support in executing all of RayzeBio clinical studies from study start-up, conduct and close-out phases.
  • Maintain and manage the study Trial Master File (TMF) in compliance with ICH-GCP and company SOPs.
  • Maintain study team SharePoint sites, study trackers and other databases, which may include data entry and filing of electronic documents.
  • Track and manage study and site essential documents.
  • Support vendor and site contract tracking and maintain contracts in applicable RayzeBio systems
  • Support organization and management of the study execution team meetings, including meeting coordination, agenda preparation and minutes.
  • Communicate effectively with all internal and external stakeholders in a positive and professional manner.
  • Participate in internal audits and inspection readiness activities.
  • Participate in teleconference calls and meetings as requested.
  • Up to 10% travel required

Education and Experience

  • Minimum 1-2 years clinical trial experience
  • Bachelor’s degree required. Life sciences or related field is preferred.

Skills and Qualifications

  • Independent professional who proactively communicates frequently and effectively.
  • Organized and able to work to on multiple projects with tight deadlines.
  • High energy level; positive attitude; works well under stress; assertive and effective communicator.
  • Hands-on, action-oriented, and able to implement effectively.

Physical Demands

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 15 pounds. Specific vision abilities required by this job include close vision and distance vision. 

Work Environment

The noise level in the work environment is usually moderate.

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If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Compensation Overview:

Remote - United States - US: $70,769 - $85,756

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee’s work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. 

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit

Company

Bristol Myers Squibb

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