$80K/yr – $90K/yr
You'll complete your application on the employer's website.
Job type
Salary
$80K/yr – $90K/yr
Sector
Posted
27 days ago
Fortrea is hiring Clinical Research Associates through its Monitoring Excellence Academy for oncology, CAR T, and ophthalmology clinical trials. The role monitors and manages study sites, protects participants, ensures protocol and regulatory compliance, reviews clinical data, and supports clinical project coordination while requiring substantial travel.
Tags
Health Care
Life Science
Pharmaceutical
Artificial Intelligence (AI)
Accounting
Human Resources
Healthcare
Publishing
Biopharma
Bookkeeping and Payroll
Employment
Freelance
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 repo11s, 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, eg. 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
Preferred
Oncology or Ophthalmology experience is strongly desired
CAR T a plus
Benefits
Remote work arrangement
AI-powered talent hiring platform for life sciences, pharma, and IT.
London, England, GBR
https://lifelancer.com
Total Funding
$0.68M
2025-03-01
Pre Seed· $0.24M
2024-03-01
Pre Seed· $0.11M
2023-03-01
Pre Seed· $0.12M
Leadership Team
Jayesh Pandya
Co-Founder & CEO
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Qualifications
strong, Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2+ years of current experience
Must have 2+ years of Oncology, CAR T or Ophthalmology experience as a CRC or research nurse
French Speaking candidates
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
2+ years as a Study Coordinator or Research Nurse in specified therapeutic areas
Strong, Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2+ years of current experience
Oncology or Ophthalmology experience is strongly desired
CAR T a plus
strong, Oncology or Ophthalmology Clinical Research Coordinators or Research Nurses with 2+ years of current experience.
Must have 2+ years of Oncology, CAR T or Ophthalmology experience as a CRC or research nurse.
Required skills
Clinical Trial Site Monitoring, Oncology, Ophthalmology, CAR T Therapy, Clinical Research Coordination, Research Nursing, Serious Adverse Event Reporting, Informed Consent Procedures, Clinical Trial Protocol Compliance, Case Report Form (CRF) Review
Preferred skills
Oncology or Ophthalmology experience is strongly desired, CAR T a plus
Experience
2+ years
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