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For Companies At a Glance
- Tasks: Monitor clinical trial sites and ensure compliance with protocols and regulations.
- Company: Join a growing CRO known for quality and collaboration in clinical trials.
- Benefits: Enjoy competitive pay, remote work flexibility, and potential long-term projects.
- Why this job: Be part of a supportive team that values your expertise and input.
- Qualifications: 2+ years CRA experience, life sciences degree, and strong GCP knowledge required.
- Other info: Opportunity to travel regionally and work on diverse clinical trials.
Now Hiring: Freelance Clinical Research Associate (CRA) – Remote (UK-Based)
Contract | Competitive Hourly Rate | Flexible Schedule
I'm working with a growing, full-service CRO that’s looking to bring an experienced Freelance CRA on board to support upcoming clinical trials. This is a great opportunity for someone who enjoys working independently, values flexibility, and wants to be part of a collaborative team environment.
About the CRO:
This is a small but expanding CRO that partners with biotech and pharma companies on early- to late-phase clinical trials. They’re known for being responsive, thorough, and committed to quality. As their study portfolio grows, they’re adding freelance CRAs to their network who can jump in and take ownership of site monitoring activities.
What You'll Be Doing:
- Monitor clinical trial sites across various stages—site selection, initiation, routine monitoring, and close-out
- Ensure sites are following protocol, GCP, and all applicable regulations
- Review source data, CRFs, and site documentation for accuracy and completeness
- Identify and follow up on any site issues or deviations
- Build strong working relationships with site staff
- Prepare and submit clear and timely visit reports
- Work closely with the internal clinical project team to keep things moving smoothly
What We're Looking For:
- At least 2 years of recent CRA experience in the U.K (independent or CRO-based)
- Strong understanding of GCP, FDA regulations, and clinical trial processes
- Background in life sciences, nursing, or a related field (Bachelor’s degree required)
- Able to work independently and manage multiple sites
- Comfortable with EDC systems and remote monitoring tools
- Based in the U.K. with ability to travel regionally as needed (up to ~60%)
Nice to Have:
- Experience with women's health, Neurology and Medical device
- Previous work with smaller CROs or sponsor teams
- A flexible, problem-solving approach
Why This Role?
- Competitive hourly pay
- Full remote flexibility + site travel
- Ongoing projects with potential for long-term collaboration
- A tight-knit team that values your input and expertise
Contact Detail:
Green Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience with smaller CROs. Attend industry events or webinars to connect with potential colleagues and learn about opportunities that may not be advertised.
✨Tip Number 2
Familiarise yourself with the specific therapeutic areas mentioned in the job description, such as women's health and neurology. This knowledge can help you stand out during interviews and demonstrate your genuine interest in the role.
✨Tip Number 3
Showcase your ability to work independently by highlighting any previous experiences where you successfully managed multiple sites or projects. Prepare examples that illustrate your problem-solving skills and flexibility in challenging situations.
✨Tip Number 4
Research the CRO's values and recent projects to tailor your conversations during interviews. Understanding their commitment to quality and responsiveness will allow you to align your answers with their expectations and culture.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate. Focus on your understanding of GCP, FDA regulations, and any specific clinical trial processes you've worked with.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your ability to work independently. Mention your experience with site monitoring and how you can contribute to the CRO's success.
Highlight Relevant Skills: In your application, emphasise skills that are crucial for the role, such as your familiarity with EDC systems, your problem-solving approach, and your ability to build strong relationships with site staff.
Proofread Your Application: Before submitting, carefully proofread your application materials. Ensure there are no typos or grammatical errors, as attention to detail is vital in clinical research.
How to prepare for a job interview at Green Life Science
✨Showcase Your CRA Experience
Make sure to highlight your previous experience as a Clinical Research Associate, especially any roles that involved site monitoring. Be prepared to discuss specific trials you've worked on and the challenges you faced, as well as how you overcame them.
✨Demonstrate Knowledge of GCP and Regulations
Since the role requires a strong understanding of Good Clinical Practice (GCP) and FDA regulations, brush up on these topics before the interview. Be ready to answer questions about how you ensure compliance during clinical trials.
✨Emphasise Your Independent Working Skills
This position values independence, so be sure to provide examples of how you've successfully managed multiple sites or projects on your own. Discuss your time management strategies and how you stay organised while working remotely.
✨Build Rapport with the Interviewer
Since the company values collaboration, try to establish a connection with the interviewer. Ask insightful questions about their team dynamics and express your enthusiasm for contributing to a supportive work environment.
