Clinical Trial Associate

Bristol Myers Squibb
$70,769 - $85,756Remote

About The Position

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on our patients. RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals. 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) according to and in compliance with corporate and program Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines and other applicable federal (FDA) and state regulations.

Requirements

  • Minimum 1-2 years clinical trial experience
  • Bachelor’s degree required.
  • 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.
  • Uses AI tools to enhance individual productivity and quality of work

Nice To Haves

  • Life sciences or related field is preferred.

Responsibilities

  • 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.

Benefits

  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
  • Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and RayzeBio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
  • Based on eligibility, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
  • All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
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