Take the next step in your clinical research career and contribute to high quality clinical studies within the medical device sector. We are looking for 2 profiles:

- a Clinical Research Associate who combines strong site management skills with a solid understanding of clinical research regulations.
- a Senior Clinical Research Associate to take ownership of clinical site performance

Ready to grow your career and make real impact? Join MindCapture!

We offer competitive salaries, a full benefits package (meal vouchers, eco vouchers, DKV health insurance, group insurance, net expense allowance and a company car). You also get the opportunity to shape your future through personalised training and development.

At MindCapture, you choose what you love, build on your strengths and make a difference where it matters most.

You will work as a MindCapture consultant for an international market leader in the healthcare industry.

Clinical Research Associate:

Job Description:

• Manage clinical study activities across multiple study sites and clinical projects

• Oversee site performance and ensure delivery of high quality clinical data within project timelines

• Conduct site visits and monitor compliance with study protocols, applicable regulations, policies and procedures

• Support the operational execution of clinical trials and the collection of substantiated clinical data

• Verify that study subject safety and wellbeing are maintained at assigned study sites

• Collaborate with clinical operations teams and study site staff to identify and resolve issues effectively

• Support corrective and preventive actions when required

• Verify that Investigator Site Files are maintained according to applicable regulations and procedures

• Support patient recruitment and retention activities

• Facilitate communication of important clinical data and study events to relevant stakeholders

• Support investigator meetings, study training activities and implementation of clinical systems and processes

• Collaborate with investigators, ethics committees, contractors, vendors and internal stakeholders

Requirements:





• Bachelor degree required, preferably in Life Sciences, Physical Sciences, Nursing or Biological Sciences

• At least two years of relevant experience with a Bachelor degree, or at least one year with a relevant advanced degree

• Previous clinical research experience required

• Previous medical device monitoring or equivalent experience required

• Strong understanding and practical application of clinical research regulations and standards for medical devices or combination products

• Relevant industry certification is preferred

• Clinical or medical background is preferred

• Experience with Microsoft Office including Excel, Word and PowerPoint

• Strong leadership, written communication, verbal communication, presentation and influencing skills

• Excellent organisational skills with the ability to manage multiple tasks simultaneously and consistently meet deadlines

• Ability to travel up to 80% of the time in Belgium

• Be able to converse and monitor in English and Dutch is required - French is preferred

Senior Clinical Research Associate

Job Description:

• Manage clinical study activities across multiple study sites and clinical projects

• Oversee assigned site performance and ensure delivery of high quality clinical data within project timelines

• Conduct site visits and monitor compliance with study protocols, applicable regulations, policies and procedures

• Support clinical trial execution while safeguarding study subject safety and wellbeing

• Ensure clinical activities follow applicable standard operating procedures, good clinical practices and regulatory requirements





• Work with clinical operations teams and study site staff to resolve issues and support corrective and preventive actions when required

• Verify that Investigator Site Files are maintained according to applicable regulations and procedures

• Support patient recruitment and retention activities

• Communicate important clinical data, study events and site status information to relevant stakeholders

• Support investigator meetings, study training activities and implementation of clinical systems and processes

• Collaborate with investigators, ethics committees, contractors, vendors and internal stakeholders

Requirements:

• Bachelor degree required, preferably in Life Sciences, Physical Sciences, Nursing or Biological Sciences

• At least four years of recent site monitoring experience

• Previous clinical research experience required

• Previous medical device monitoring or equivalent experience required

• Strong understanding and practical application of clinical research regulations and standards for medical devices or combination products

• Relevant industry certification is preferred

• Clinical or medical background is preferred

• Experience with Microsoft Office including Excel, Word and PowerPoint

• Strong leadership, written communication, verbal communication, presentation and influencing skills

• Excellent organisational skills with the ability to manage multiple tasks simultaneously and consistently meet deadlines

• Ability to travel up to 80% of the time in Belgium

• Be able to converse and monitor in English and Dutch is required - French is preferred

Are you ready to make a real difference in healthcare?

Join our dynamic team and help drive innovation in medical devices.

Apply now and let’s make an impact together!

Want to learn more? Discover all opportunities at www.mindcapture.com.

If MindCapture sees a potential fit, we’ll get in touch as soon as possible.

If you don’t hear from us within two weeks, it simply means that this particular position wasn’t the right match. In that case, we’ll gladly keep your profile in mind for future roles that could suit you better.

📌 Clinical research associate (España)
🏢 MindCapture
📍 España