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For Companies At a Glance
- Tasks: Oversee clinical trials, train staff, and support live procedures with medical devices.
- Company: Join a leading organisation dedicated to advancing medical research and technology.
- Benefits: Enjoy flexible working options, travel opportunities, and a chance to make a real impact.
- Why this job: Be part of a collaborative team that values innovation and patient care in healthcare.
- Qualifications: Bachelor's degree in life sciences; experience in clinical trials and proctoring preferred.
- Other info: Willingness to travel 60-80% within the EU is required.
The predicted salary is between 36000 - 60000 £ per year.
The position includes a diverse set of duties. In addition to your critical role in overseeing and managing clinical trials, you will take on advanced proctoring responsibilities. As a Clinical Specialist, you will train study site staff on the correct use of the study device and provide input during live cath lab procedures. Periodic technical case support at investigator sites is also expected to ensure safe and effective use of the medical technology, meeting study protocols. If you are a proactive, collaborative, service-minded, and detail-oriented individual with a passion for advancing medical research and a proven track record in medical device clinical trials, we encourage you to apply.
Key Responsibilities
- Proctoring and Case Support Duties
- Train assigned study staff on the correct use of the study device.
- Supervise/support the setup of the required site workflow to ensure ideal basis for enrolment and that study images and measurements are collected and of consistent quality.
- Maintain detailed proctoring records and documentation.
- Assist remotely or on site during live cases by supporting site staff in the correct use of the study device and the CIP.
- In agreement with CPM, release clinical sites to independent use of the study device.
- Manage clinical trial activities in alignment with the clinical project manager (CPM), from study initiation, enrolment to study close-out.
- Train and educate site staff on study CIP, the correct use of the study EDC software, the electronic Investigator Site File (eISF), and regulatory requirements.
- Conduct site qualification, initiation, monitoring, and close-out visits to ensure CIP adherence and data integrity.
- Collaborate with investigators and study site staff to resolve issues and ensure timely and accurate data collection.
- Work in close collaboration with the study-assigned CRO (if applicable).
Desired Qualifications
- Bachelor's degree in a relevant life science or healthcare field, master's degree preferred.
- Relevant experience as Clinical Field Trial Specialist, Field Technical Specialist or similar.
- Proven experience in proctoring and site management preferred.
- Strong organizational skills and attention to detail.
- Good communication and interpersonal skills.
- Ability to work independently and collaboratively in a fast-paced environment.
- Proficiency in additional languages (Italian, German, and/or Spanish) are preferred.
- Willingness to travel up to 60-80% within EU.
Clinical Specialist employer: Skills Alliance
Contact Detail:
Skills Alliance Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Specialist
✨Tip Number 1
Familiarise yourself with the latest trends and technologies in clinical trials, especially those related to medical devices. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals already working in clinical trials or medical device sectors. Attend relevant conferences or webinars to connect with potential colleagues and learn about their experiences, which can provide valuable insights for your application.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences that showcase your skills in proctoring and site management. Being able to articulate how you've successfully trained staff or managed clinical trial activities will set you apart.
✨Tip Number 4
If you speak any additional languages, be sure to highlight this during your interactions. Proficiency in languages like Italian, German, or Spanish can be a significant advantage, especially when working with diverse study sites across the EU.
We think you need these skills to ace Clinical Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials and proctoring. Emphasise any specific roles where you trained staff or managed clinical activities, as these are key responsibilities for the Clinical Specialist position.
Craft a Compelling Cover Letter: In your cover letter, express your passion for advancing medical research and detail your proactive approach to problem-solving. Mention specific examples of how you've successfully collaborated with teams in previous roles.
Highlight Relevant Qualifications: Clearly state your educational background and any relevant certifications. If you have experience with electronic data capture (EDC) software or regulatory requirements, make sure to include that information.
Showcase Communication Skills: Since good communication is essential for this role, provide examples of how you've effectively communicated with diverse teams or stakeholders in past positions. This could be through training sessions, presentations, or collaborative projects.
How to prepare for a job interview at Skills Alliance
✨Showcase Your Clinical Knowledge
Make sure to highlight your understanding of clinical trials and medical devices during the interview. Be prepared to discuss your previous experiences in managing clinical trials and how you ensured compliance with study protocols.
✨Demonstrate Training Skills
Since training site staff is a key responsibility, be ready to provide examples of how you've successfully trained others in the past. Discuss your approach to ensuring that everyone understands the correct use of medical technology.
✨Emphasise Collaboration
This role requires working closely with various stakeholders. Share examples of how you've collaborated with investigators and site staff to resolve issues and ensure data integrity. Highlight your ability to work both independently and as part of a team.
✨Prepare for Technical Questions
Expect to answer technical questions related to the study device and clinical trial processes. Brush up on relevant regulations and best practices in clinical research to demonstrate your expertise and confidence.
