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Senior Clinical Research Associate

Life Sciences
Clinical
Medior (3+)
Location
Machelen, Flemish Brabant
Work type
Consultancy
Work model
Fulltime, Hybrid

Our client, a leading player in the MedTech industry, is seeking a Senior Clinical Research Associate to manage clinical study activities across multiple sites. This role focuses on overseeing study site performance, conducting comprehensive monitoring visits, and ensuring high-quality data collection for various medical device projects.

Responsibilities

  • Manage clinical study activities and site performance for multiple projects according to overall project timelines.
  • Conduct site visits, monitoring, and communication to ensure compliance with study protocols and regulatory requirements.
  • Oversee the maintenance of Investigator Site Files and ensure the safety and well-being of study subjects are maintained.
  • Support patient recruitment and retention activities while resolving site-level issues through corrective and preventive actions.
  • Execute clinical trials in alignment with established standard operating procedures, GCP, and relevant regulatory standards.
  • Collaborate with investigators, IRBs/ECs, and vendors to support the implementation of new clinical systems and processes.

Requirements

  • You have a Bachelor degree in Life Sciences, Nursing, or a related field.
  • You have 4+ years of recent experience in site monitoring within clinical research, specifically for medical devices.
  • You possess a strong understanding of GCP and regulatory standards applied to medical devices and combination products.
  • You bring experience working with computer systems including Microsoft Office (Excel, Word, and PowerPoint).
  • You're characterized by leadership abilities and strong organizational skills to manage multiple tasks and deadlines simultaneously.
  • You are willing to travel up to 80% of the time to support site visits and clinical activities.
  • You are fluent in English and Dutch with the ability to converse and review medical documentation.

Nice to Haves

  • Industry certifications such as CCRA, RAC, or CDE.
  • Clinical or medical background.
  • Working knowledge of French.

Offer

  • Enjoy a competitive salary package with extra perks that recognize your talent.
  • Advance your career with a clear growth path, coaching, and mentoring to support you.
  • Thrive in a dynamic and supportive environment where you can truly make an impact.
  • Work when and where you perform best, ensuring an optimal work-life balance.
  • Choose a flexible transport solution, from a company car to a public transport subscription.
  • Expand your network and enjoy unforgettable moments at exclusive events and afterworks.
  • Grow your skills with external courses and our in-house Pauwels Academy.
  • Work on exciting projects with industry leaders in Life Sciences, Engineering & Digital.
  • Seize opportunities at every level, from a strong start to career acceleration and expert collaboration.
# 102693
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Candidates must be legally authorised to work in the EU and possess the required language skills for the job location.
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