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- Tasks: Conduct on-site and remote oversight for clinical trials, ensuring compliance and data integrity.
- Company: Join a dynamic team focused on colorectal cancer research and patient safety.
- Benefits: Enjoy flexible part-time hours and the opportunity to travel across the UK and EU.
- Why this job: Make a real impact in clinical research while gaining valuable experience in a supportive environment.
- Qualifications: Must have CRA experience, strong GCP knowledge, and excellent communication skills.
- Other info: This role is currently in the pipelining stage, with engagement expected soon.
The predicted salary is between 36000 - 60000 £ per year.
Job Title: Clinical Research Associate (CRA) – Part-Time Consultant / ContractorLocation: United Kingdom (with regional travel to study sites in the UK and EU)Contract Type: Part-Time Consultancy / Freelance ContractStudy Area: Colorectal CancerOverviewWe are seeking an experienced Clinical Research Associate (CRA) level consultant to provide supplemental on-site and remote oversight in addition to CRO monitoring activities. This role will act as an extension of the sponsor’s team, ensuring compliance with protocol, Good Clinical Practice (GCP), and applicable regulatory requirements.The position will focus on targeted, high-value oversight activities at clinical sites to safeguard data integrity, patient safety, and study compliance.Key Responsibilities• Perform targeted on-site visits to verify protocol adherence, data accuracy, and correct handling of biological samples, with emphasis on high-risk procedures and critical endpoints.• Observe study conduct and review source documentation to confirm appropriate sample processing and chain-of-custody.• Escalate potential compliance or data quality risks to the sponsor in real time.• Act as a liaison between site staff, the sponsor, and CRO monitors to facilitate timely issue resolution.• Apply lessons learned from prior studies to proactively identify and mitigate operational risks.• Document all oversight activities in accordance with sponsor quality management procedures.• Contribute to ongoing risk assessments throughout the course of the study.Preliminary Study Details• UK Sites: 3 to 4• Enrollment: 3 to 5 patients per siteRequirements• Proven experience as a CRA, ideally with both on-site and remote monitoring exposure in the EU and UK.• Strong working knowledge of ICH GCP, clinical trial regulations, and sponsor oversight practices.• Excellent communication skills in English, including written, spoken, and reading comprehension.• Ability to work independently while maintaining a high level of communication with the sponsor team.• Flexible to occasionally work US East Coast hours to align with the sponsor’s team.• Willingness and ability to travel regionally within the UK and EU.• Experience in colorectal or similar therapeutic areas is preferred.Contract Details• Part-time, time and materials basis.• Travel up and down the UK• Engagement length and hours to be agreed upon based on study needs.NoteThis role is currently in the pipelining stage. We are confident that feedback will be received in the coming weeks, enabling engagement with suitable talent promptly thereafter.
Freelance Clinical Research Associate employer: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Freelance Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field, especially those who have experience as a CRA. Attend industry conferences or local meetups to connect with potential colleagues and learn about job opportunities that may not be advertised.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to clinical trials, particularly ICH GCP. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Consider reaching out to previous employers or colleagues for references or recommendations. A strong endorsement from someone in the industry can significantly enhance your chances of landing the role.
✨Tip Number 4
Stay updated on current trends and developments in colorectal cancer research. Being knowledgeable about the specific study area will help you engage in meaningful conversations during interviews and showcase your expertise.
We think you need these skills to ace Freelance Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience as a Clinical Research Associate, particularly any on-site and remote monitoring roles. Emphasise your knowledge of ICH GCP and clinical trial regulations.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the job description. Mention your experience in colorectal cancer studies and how you can contribute to safeguarding data integrity and patient safety.
Showcase Communication Skills: Since excellent communication is crucial for this role, provide examples in your application that demonstrate your ability to liaise effectively with site staff, sponsors, and CRO monitors.
Highlight Flexibility and Travel Willingness: Clearly state your willingness to travel regionally within the UK and EU, and your flexibility to work US East Coast hours. This shows your commitment to meeting the study's needs.
How to prepare for a job interview at LinkedIn
✨Showcase Your Experience
Be prepared to discuss your previous roles as a Clinical Research Associate, especially any experience with on-site and remote monitoring. Highlight specific projects you've worked on, particularly in colorectal cancer or similar therapeutic areas.
✨Demonstrate Knowledge of Regulations
Familiarise yourself with ICH GCP guidelines and clinical trial regulations. During the interview, be ready to explain how you ensure compliance and data integrity in your work, as this is crucial for the role.
✨Communication is Key
Since the role requires liaising between site staff, sponsors, and CRO monitors, practice articulating your thoughts clearly. Prepare examples of how you've effectively communicated in past roles, especially in resolving issues.
✨Be Ready to Discuss Travel Flexibility
As the position involves regional travel within the UK and EU, be honest about your availability and willingness to travel. Mention any previous experiences that required travel and how you managed your time effectively.