operations
Posted May 13Clinical Operations Coordinator
at Fortrea
On-site
Responsibilities
- Support study documentation activities , including preparing, reviewing, and quality‑checking study‑specific and participant‑facing documents, and ensuring documentation is accurate, complete, and correctly used during live trial activity.
- Oversee and coordinate live clinic activity across the full participant journey , from participant check‑in through to the last participant visit, ensuring that clinic workflows follow the approved protocol and SOPs.
Requirements
- Step in when required to perform basic clinical tasks , such as taking vitals, to support the team during peak study activity. QUALIFICATIONS/
- EXPERIENCE Fortrea may consider relevant and equivalent experience in lieu of educational
- requirements . University/college degree in life science, pharmacy or related subject, or certification in a related allied health profession (e.g. nursing). In lieu of a degree, typically 3 years’
- experience in a related field will be considered. To succeed in this job, you will bring: 2 years´
- experience working in clinical trials , on a CRO, Phase I unit, hospital research setting or similar .
- Backgrounds that translate well into this role include: Research Technicians, Clinical Operations Staff, Study Support roles, etc. Practical understanding of clinical trial protocols and procedures , and how these translate into site‑level execution in line with SOPs and GCPs.
- Experience managing multiple studies or workstreams in parallel, remaining organised and effective in a fast‑paced, live clinical research environment.
- Willingness and ability to step in to perform basic clinical tasks when required, such as taking vitals, following appropriate training and delegation Strong attention to detail and organisational skills , particularly when supporting study documentation and ensuring information is accurate and complete Strong written communication skills in English , particularly when working with clinical documentation and protocol‑driven materials.
Benefits
- These will be compensated with extra pay or flexi time.