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CTA Job at Bristol Myers Squibb | Remote Clinical Trial Associate Opportunity, Apply Online

CTA Job Opportunity at Bristol Myers Squibb | Apply Now

CTA job opportunities continue to attract clinical research professionals looking to advance their careers in clinical operations. Bristol Myers Squibb (BMS), through its subsidiary RayzeBio, is hiring a Clinical Trial Associate for a remote position in the United States. This exciting role offers the chance to support innovative oncology clinical trials while working with a leading biotechnology company focused on developing transformative radiopharmaceutical therapies for cancer patients.

  • Job Position: Clinical Trial Associate, Clinical Operations
  • Company: Bristol Myers Squibb (BMS) – RayzeBio
  • Location: Remote – United States
  • Job ID: R1603279
  • Salary Range: $70,769 – $85,756 annually

About the Company

CTA job seekers interested in oncology research will find an exciting opportunity with Bristol Myers Squibb and RayzeBio. RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is a dynamic biotechnology company headquartered in San Diego, California. The company focuses on improving survival outcomes for people living with cancer by harnessing the power of targeted radioisotopes. RayzeBio develops innovative therapies targeting solid tumors and aims to become a global leader in radiopharmaceuticals.

As part of the broader BMS careers network, employees benefit from the resources, expertise, and global reach of one of the world’s leading oncology innovators while working in a highly collaborative and entrepreneurial environment.

CTA job Description

CTA job responsibilities involve providing project system, tracking, and administrative support across all phases of clinical study activities. The Clinical Trial Associate (CTA) serves as an integral member of the Clinical Operations team and supports clinical studies through feasibility, start-up, maintenance, and close-out activities. The role ensures compliance with Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, FDA regulations, and other applicable requirements. This remote job offers the opportunity to contribute directly to the successful execution of clinical trials that may help transform cancer treatment.

Qualifications

CTA job applicants should possess relevant clinical trial experience and strong organizational skills.

Education

Experience

  • Minimum of 1–2 years of clinical trial experience.

Skills 

  • Strong organizational and multitasking abilities.
  • Ability to work on multiple projects with tight deadlines.
  • Excellent verbal and written communication skills.
  • High energy level and positive attitude.
  • Action-oriented and capable of effective implementation.
  • Ability to work independently while collaborating across teams.
  • Experience using AI tools to enhance productivity and quality of work.

CTA job – Key Responsibilities

CTA job duties include supporting study teams and maintaining critical trial documentation throughout the clinical trial lifecycle.

  • Support study execution teams during study start-up, conduct, and close-out phases.
  • Maintain and manage the Trial Master File (TMF) in compliance with ICH-GCP and company SOPs.
  • Manage study trackers, SharePoint sites, databases, and essential study documents.
  • Track vendor and site contracts and maintain records in RayzeBio systems.
  • Coordinate study meetings, agendas, and meeting minutes.
  • Communicate effectively with internal and external stakeholders.
  • Assist with audits, inspection readiness activities, and team meetings.
  • Travel up to 10% as required.

CTA job – Conclusion

CTA job opportunities at Bristol Myers Squibb and RayzeBio provide an excellent pathway for clinical research professionals looking to build a successful career in clinical operations. With a competitive salary, strong benefits package, remote flexibility, and the chance to contribute to innovative oncology research, this position represents an outstanding opportunity within the growing clinical research industry.

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