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- Tasks: Manage and support clinical trials across Europe, ensuring compliance and data accuracy.
- Company: Leading pharmaceutical company focused on innovative clinical research.
- Benefits: Competitive salary, travel opportunities, and professional development in a dynamic field.
- Why this job: Join a high-impact role that combines travel with cutting-edge medical technology.
- Qualifications: Experience in clinical research and familiarity with surgical environments required.
- Other info: Flexible work environment with excellent career growth potential.
The predicted salary is between 36000 - 60000 ÂŁ per year.
We are seeking an experienced Clinical Research Associate (CRA) or Site Manager to manage and support the execution of clinical trials across multiple sites in Europe, including the UK, Spain, Italy, Germany, France, and Netherlands. The role will involve high travel, site management, data collection, and protocol setup across a variety of surgical settings, with a strong focus on data management and clinical operations.
Location: Europe (UK-based with high travel to sites in Spain, Italy, Germany, France, Netherlands)
Travel Requirement: High (to 5-6 sites across Europe)
Key Responsibilities
- Site Management & Monitoring: Oversee the execution and monitoring of clinical trials at 5-6 sites across Europe, ensuring trial compliance with GCP, regulatory guidelines, and clinical protocols. Manage site startup activities, monitor progress, and perform regular site visits to ensure highâquality data collection and patient safety. Conduct regular site training and followâup visits to ensure adherence to study protocols.
- Data Management: Oversee and ensure accurate data entry into relevant databases, including data verification and video management from sites. Assist with the setup of clinical protocols, monitoring data quality, resolving discrepancies, and collaborating with the data management team to ensure data accuracy, completeness, and compliance. Prepare and assist with data demo sessions as needed.
- Clinical Research & Medical Tech Experience: Demonstrate knowledge of medical technology, particularly operatingâroom settings, including laparoscopic and robotic surgery. Experience in colorectal surgery, soft tissue, general surgery, and gynaecology. Familiarity with laparoscopy, minimally invasive techniques, and robotic surgery is essential. No orthopaedic or catheter lab experience required.
- Regulatory Compliance & Support: Work closely with clinical teams to ensure regulatory compliance, patient safety, and trial integrity across all study sites. Support preparation of required documentation, including protocol amendments and clinical trial reports. Ensure sites remain inspectionâready with a proactive approach to quality control and audit preparation.
Skills & Experience
- Clinical Research Experience: Previous experience as a CRA, Site Manager, or similar role in clinical research and trial management. Experience with data management, including data entry, quality control, and study setup. Background in medical technology or clinical trials involving medical devices is a plus.
- Surgical & OR Experience: Handsâon experience or familiarity with operatingâroom environments, specifically in laparoscopic, robotic surgery, and other minimally invasive techniques. Experience in colorectal surgery, soft tissue, general surgery, and gynaecology is highly desirable.
- Language & Communication Skills: English proficiency required for communication with sites across Europe. Knowledge of Japanese would be an asset but is not essential.
- Flexibility & Travel: High travel across European sites; flexibility and independent workload management are essential. Ability to take ownership of trial progress with minimal supervision.
Additional Information
- Other Details: This is not a super-fast process; we are looking for someone with the right experience who can take on a highâvisibility, highly flexible role. The role will primarily involve data management, with the opportunity to demonstrate clinical tech in surgical environments. Budget is available for the right candidate, but the timeline is not short, allowing careful selection. We prefer a gentle approach to avoid overwhelming sites.
Seniority level: Associate
Employment type: Fullâtime
Job function: Project Management
Industries: Pharmaceutical Manufacturing and Biotechnology Research
Clinical Research Associate/ Clinical Site Manager in London employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice đ¤Ť
We think this is how you could land Clinical Research Associate/ Clinical Site Manager in London
â¨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online forums. We all know that sometimes itâs not just what you know, but who you know that can help you land that CRA or Site Manager role.
â¨Tip Number 2
Prepare for those interviews by brushing up on your knowledge of GCP and regulatory guidelines. We want you to be able to discuss your experience with data management and site monitoring confidently. Practice common interview questions and have examples ready to showcase your skills!
â¨Tip Number 3
Donât forget to tailor your approach! When applying through our website, make sure your CV and cover letter highlight your specific experience in surgical settings and data management. We want to see how your background aligns with the role of Clinical Research Associate or Site Manager.
â¨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the position. We recommend reiterating your interest in the role and mentioning something specific from the interview to keep you fresh in their minds.
We think you need these skills to ace Clinical Research Associate/ Clinical Site Manager in London
Some tips for your application đŤĄ
Tailor Your CV: Make sure your CV is tailored to the role of Clinical Research Associate or Site Manager. Highlight your relevant experience in clinical trials, data management, and any surgical settings you've worked in. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your skills make you a great fit for our team. Don't forget to mention your flexibility and willingness to travel across Europe â it's a big part of the job!
Showcase Your Communication Skills: Since you'll be working with sites across Europe, it's crucial to demonstrate your communication skills in your application. Whether it's through your CV or cover letter, let us know how you've effectively communicated in past roles, especially in high-pressure environments.
Apply Through Our Website: We encourage you to apply directly through our website. Itâs the best way for us to receive your application and ensures youâre considered for the role. Plus, it shows us that you're proactive and keen to join our team at StudySmarter!
How to prepare for a job interview at Barrington James
â¨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials, especially those related to surgical settings. Be prepared to discuss your previous experiences managing trials and how you ensured compliance with GCP and regulatory guidelines.
â¨Showcase Your Data Management Skills
Since data management is a key part of this role, be ready to talk about your experience with data entry, quality control, and resolving discrepancies. Bring examples of how you've collaborated with data management teams in the past.
â¨Familiarise Yourself with Surgical Environments
Given the focus on laparoscopic and robotic surgery, itâs crucial to demonstrate your understanding of these techniques. If you have hands-on experience, share specific instances where you applied your knowledge in an operating-room setting.
â¨Prepare for High Travel Discussions
With high travel requirements, be ready to discuss your flexibility and how you manage workloads independently. Highlight any previous roles that involved significant travel and how you maintained productivity while on the move.
