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- Tasks: Support clinical trials by planning, organising, and conducting monitor visits across the UK.
- Company: Dynamic company in the pharmaceutical and biotech sectors with a diverse team.
- Benefits: Flexible home office options, modern offices, and support from experienced professionals.
- Why this job: Make a real difference in patients' lives while working on exciting projects.
- Qualifications: Relevant medical qualification and strong communication skills; CRA experience is a plus.
- Other info: Join a diverse team with flat hierarchies and opportunities for growth.
The predicted salary is between 36000 - 60000 £ per year.
You support project management in the planning, organisation, and implementation of national and international clinical trials in phases II to IV. You conduct monitor visits (initiation, monitoring of ongoing trial activities, and close-out) in accordance with SOPs and applicable guidelines across the UK. You work closely with the trial centers and the relevant departments of the sponsor.
You prepare study-related documents (e.g., for authorities and ethics committees) and project plans, select potential trial centers, prepare training courses and presentations, and conduct these independently.
You are a scientist, physician, or have a relevant qualification in the medical field. It would be advantageous if you already have professional experience as a CRA or have successfully completed basic CRA training. You have strong communication skills and fluency in English. Additional excellent language skills and knowledge of ICH-GCP guidelines are an advantage but not a requirement.
You are flexible when the role requires. You are organised, punctual, have great interpersonal skills and happy to work with the team. You have an entitlement to work in the UK. You have a UK drivers licence.
We ensure you a thorough introduction and support from a team of experienced natural scientists. We offer exciting and varied projects from the pharmaceutical, biotech and medical production sectors. We guarantee fast decision-making processes due to flat hierarchies and “open doors” culture. We love diversity! Our teams are diverse, cross-generational and we work and learn with and from each other. We have modern, well-equipped offices. We provide flexible home office options with a minimum of 1 day per week in the office.
We invite you to join us in making a lasting difference in the lives of countless patients. Every day anew. We are looking forward to your application.
Clinical Research Associate (CRA) / Monitor (f/m/d) in Guildford employer: FGK Clinical Research GmbH
Contact Detail:
FGK Clinical Research GmbH Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate (CRA) / Monitor (f/m/d) in Guildford
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that CRA role.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP guidelines and recent developments in clinical trials. We want you to shine when discussing your experience and how it aligns with the job!
✨Tip Number 3
Showcase your organisational skills! During interviews, share examples of how you've managed multiple tasks or projects. We love hearing about your ability to juggle responsibilities effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. We’re excited to see what you bring to the table!
We think you need these skills to ace Clinical Research Associate (CRA) / Monitor (f/m/d) in Guildford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Clinical Research Associate role. Highlight any relevant qualifications, especially in the medical field, and don’t forget to mention your communication skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical trials and how your background makes you a great fit for our team. Keep it engaging and personal!
Showcase Your Experience: If you’ve got experience as a CRA or have completed CRA training, make sure to highlight that! Even if you haven’t, any related project management or clinical trial experience can set you apart.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity with StudySmarter!
How to prepare for a job interview at FGK Clinical Research GmbH
✨Know Your Clinical Trials
Familiarise yourself with the phases of clinical trials, especially II to IV, as well as the specific guidelines and SOPs relevant to the role. Being able to discuss recent trials or advancements in the field will show your passion and knowledge.
✨Showcase Your Communication Skills
Since strong communication is key for a CRA, prepare examples of how you've effectively communicated with teams or trial centres in the past. Practice articulating your thoughts clearly and confidently, as this will be crucial during the interview.
✨Demonstrate Organisational Skills
Be ready to discuss how you manage multiple tasks and projects simultaneously. Share specific strategies or tools you use to stay organised, as this role requires juggling various responsibilities from planning to monitoring.
✨Emphasise Teamwork and Flexibility
Highlight your ability to work collaboratively within a team and adapt to changing circumstances. Prepare anecdotes that illustrate your flexibility and how you’ve contributed positively to team dynamics in previous roles.
