Remote Oncology CAR‑T CRA Lead (Sr. CRA)

Fortrea; Michigan; On-site; USD 105,000 - 145,000; Full time

Benefits offered by this job

Medical, Dental, Vision, Life, STD/LTD

401(K)

Paid time off (PTO) – Flex Plan

Employee recognition awards

Multiple ERG’s

Job summary

Fortrea is seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team, working with various sponsors. 1+ year of independent CRO/sponsor monitoring required; CAR‑T desired. Open to major hub locations across the US with 60-70% travel and 8-10 DOS per month.

You will monitor sites, manage data integrity, ensure regulatory compliance, and support registry activities. The role emphasizes teamwork, adaptability, and strong clinical judgment in a fast-paced environment.

Qualifications

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure).
• 1+ years of Clinical Monitoring experience.
• Oncology experience is desired.
• Open to various hub locations.

Responsibilities

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.
• Responsible for all aspects of site management as prescribed in the project plans.
• General On-Site Monitoring.
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.
• Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document monitor data for missing or implausible data.
• Responsible for all aspects of registry management as prescribed in the project plans - undertake feasibility work when requested.
• Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
• Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management.
• Assist with training of new employees, e.g., co‑monitoring.
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned.
• Perform other duties as assigned by management.

Skills

1+ years Clinical Monitoring

Oncology experience

Education

University or college degree, or certification in allied health

Job description

Fortrea is seeking Experienced Oncology CRAs to lead and support our Full Service Outsourcing team, working with various sponsors. 1+ year of independent CRO/sponsor monitoring required; CAR‑T desired. Open to major hub locations across the US with 60-70% travel and 8-10 DOS per month.

You will monitor sites, manage data integrity, ensure regulatory compliance, and support registry activities. The role emphasizes teamwork, adaptability, and strong clinical judgment in a fast-paced environment.