At a Glance
- 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.
- Other info: High visibility role with flexible working and excellent career growth potential.
- Why this job: Join a vital role in advancing medical technology and improving patient outcomes.
- Qualifications: Experience in clinical research and familiarity with surgical environments required.
The predicted salary is between 36900 - 45100 £ 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 high-quality data collection and patient safety. Conduct regular site training and follow-up 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 operating-room 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 inspection-ready 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: Hands-on experience or familiarity with operating-room 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
- This is not a super-fast process; we are looking for someone with the right experience who can take on a high-visibility, 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: Full-time
Job function: Project Management
Industries: Pharmaceutical Manufacturing and Biotechnology Research
Clinical Research Associate/ Clinical Site Manager in England employer: Barrington James
Barrington James is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in Epidemiology and Real-World Evidence. With a strong emphasis on employee growth, we offer tailored development opportunities and the chance to lead impactful projects across diverse therapeutic areas in the dynamic UK/Europe market. Join us to be part of a team that values flexibility, creativity, and meaningful contributions to healthcare advancements.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate/ Clinical Site Manager in England
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We think you need these skills to ace Clinical Research Associate/ Clinical Site Manager in England
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Barrington James!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Barrington James that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Barrington James!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Barrington James, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Barrington James
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Barrington James that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
