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- Tasks: Support clinical trials from start to finish, ensuring compliance and smooth operations.
- Company: Join a leading Biotech making waves in groundbreaking clinical research.
- Benefits: Enjoy a hybrid work model with remote flexibility and a dynamic team environment.
- Why this job: Be part of innovative research that shapes the future while developing your skills.
- Qualifications: Previous experience as a Clinical Trial Associate or similar role is essential.
- Other info: Work in London office 2 days a week; the rest is remote!
The predicted salary is between 36000 - 60000 £ per year.
Are you a passionate and skilled Clinical Trial Associate looking for a flexible, dynamic role? Join a leading Biotech as a Freelance Clinical Trial Associate and contribute to groundbreaking clinical research while enjoying a hybrid work arrangement!
Role Overview: As a Freelance Clinical Trial Associate (CTA), you'll play a key role in supporting the management and execution of clinical trials. You’ll work with a talented team, ensuring the smooth progress of studies, from start-up through to close-out, all while adhering to regulatory standards.
Location: London Office (2 days per week) Work remotely the rest of the time!
Key Responsibilities:- Assist in the preparation and submission of study documents.
- Support the management of clinical trial sites and vendors.
- Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
- Maintain study-related documentation and databases.
- Coordinate and communicate with stakeholders, including monitors, investigators, and clinical teams.
- Previous experience as a Clinical Trial Associate (CTA) or similar clinical role.
- Knowledge of clinical trial processes and GCP.
- Strong organizational and communication skills.
- Ability to work independently and as part of a team.
- Availability to be in the office in London for 2 days per week.
Interested? Apply now and be part of an innovative team shaping the future of clinical research!
Freelance Clinical Trial Associate employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Freelance Clinical Trial Associate
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry events or webinars to connect with current Clinical Trial Associates and learn about their experiences. This can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, especially Good Clinical Practice (GCP). Being knowledgeable about current standards will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Prepare to discuss specific examples from your previous experience that highlight your organisational and communication skills. Think of scenarios where you successfully managed multiple tasks or coordinated with various stakeholders, as these are crucial for a Freelance CTA.
✨Tip Number 4
Showcase your adaptability and ability to work independently. Since this role involves a hybrid work arrangement, be ready to explain how you manage your time and stay productive while working remotely, as well as how you collaborate effectively with a team.
We think you need these skills to ace Freelance Clinical Trial Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience as a Clinical Trial Associate or in similar clinical roles. Emphasise your knowledge of clinical trial processes and Good Clinical Practice (GCP) to align with the job requirements.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your ability to work both independently and as part of a team. Mention specific examples from your previous roles that demonstrate your organisational and communication skills.
Highlight Flexibility: Since this role offers a hybrid work arrangement, mention your adaptability and willingness to work in the London office two days a week. This shows you are ready to meet the company's needs while enjoying the flexibility they offer.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical trial management.
How to prepare for a job interview at Barrington James
✨Showcase Your Experience
Be prepared to discuss your previous experience as a Clinical Trial Associate or in a similar role. Highlight specific projects you've worked on, focusing on your contributions and the outcomes achieved.
✨Demonstrate Knowledge of GCP
Familiarise yourself with Good Clinical Practice (GCP) guidelines and be ready to discuss how you have applied these in your past roles. This will show your understanding of regulatory standards and compliance.
✨Emphasise Communication Skills
Since the role involves coordinating with various stakeholders, be sure to highlight your communication skills. Prepare examples of how you've effectively communicated with team members, monitors, and investigators in previous positions.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's clinical trials and their approach to research. This not only shows your interest in the role but also demonstrates your proactive attitude towards understanding the company’s goals.
