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- 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 for long-term projects.
- Why this job: Be part of a supportive team while making an impact in healthcare research.
- Qualifications: 2+ years CRA experience, life sciences degree, and knowledge of GCP and FDA regulations.
- Other info: Ideal for those who thrive in independent roles and enjoy problem-solving.
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 UK (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.S. 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
Clinical Research Associate employer: Green Life Science
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 more about the company culture.
✨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 discussions and demonstrate your genuine interest in the role.
✨Tip Number 3
Prepare to discuss your experience with EDC systems and remote monitoring tools in detail. Be ready to share specific examples of how you've successfully used these tools in past roles to enhance site monitoring.
✨Tip Number 4
Showcase your problem-solving skills by preparing examples of challenges you've faced in previous CRA roles and how you overcame them. This will highlight your ability to adapt and thrive in a flexible work environment.
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, especially your understanding of GCP and FDA regulations. Include specific examples of your work with clinical trials and any experience with EDC systems.
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 commitment to quality.
Highlight Relevant Skills: In your application, emphasise skills that are particularly relevant to the role, such as problem-solving, relationship-building with site staff, and your ability to manage multiple sites effectively.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at Green Life Science
✨Showcase Your CRA Experience
Make sure to highlight your relevant experience as a Clinical Research Associate, especially any specific projects you've worked on. Discuss your familiarity with GCP and FDA regulations, as well as your ability to manage multiple sites effectively.
✨Demonstrate Your Problem-Solving Skills
Since the role requires a flexible, problem-solving approach, prepare examples of challenges you've faced in previous roles and how you overcame them. This will show your potential employer that you can handle the demands of the job.
✨Familiarise Yourself with EDC Systems
As comfort with EDC systems and remote monitoring tools is essential, be ready to discuss your experience with these technologies. If you have specific examples of how you've used them to improve site monitoring, share those during the interview.
✨Build Rapport with the Interviewer
Since this role involves building strong relationships with site staff, it's important to demonstrate your interpersonal skills during the interview. Engage with the interviewer, ask questions, and show genuine interest in their team and projects.
