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(Senior) Clinical Research Associate (NL/EN)

  • Locatie:

    Brussel, België

  • Contactpersoon:

    Aurore Munaut

  • Contractsoorten:


  • Telefoon contactpersoon:

    +32 10 68 53 31

  • Bedrijfssectoren:

    Life Sciences

  • E-mail contactpersoon:

Do you have recent clinical monitoring experience as CRA, a special interest in cardiology and are you fluent in Dutch and English ?
Check out the position below, this exciting international CRA opportunity in the dynamic world of medical devices may be your next challenge !

Job Description

This individual will be responsible for managing clinical activities at study sites conducting studies for the Medical Devices group, as well as, fostering strong, productive relationships with colleagues within the
Medical Devices Group.

Responsible for managing clinical study activities for multiple sites in single or several clinical projects. Oversees performance of appointed study sites, conducting company initiated clinical studies. Responsible for the site visits, monitoring, communication, and deliverables for the assigned study sites. Serves as a member of the clinical study team and is the liaison between Clinical Operations and study site personnel for the specific clinical projects.


Clinical Study Site Management Tasks

  • Ensures that all work related activities, and decisions embody the Client Values.
  • Verify safety and well being of study subjects are maintained for assigned study sites.
  • Support the operational execution of clinical trials and ensure collection of high quality, substantiated data.
  • Execute clinical trials activities following established standard operating procedures, good clinical practices and regulatory requirements.
  • Accountable for study site performance, and providing high quality data according to overall project timeline.
  • Assist Clinical Operations staff and study site staff to quickly and effectively resolve issues. Responds to problems and assists in implementing corrective and preventive actions, if required.
  • Verify Investigator Site Files at assigned study sites are maintained according to regulations and/or company requirements/procedures.
  • Responsible for supporting patient recruitment and retention activities.
  • Performs site visits and ensures study site is compliant with the study protocol and all Federal, State, local, and company regulations, policies and procedures.
  • Assists with internal communication of important clinical data and events.
  • Support organization of Investigator and other study training meetings, if required.
  • Functions as a reliable, trusted resource of accurate, up-to-date study site status knowledge, as requested by key stakeholders.
  • Understand business value of clinical projects and balances overall business objectives and functional needs.
  • May be involved in other tasks to support Clinical Operations and Operating Company as needed.
  • Support the implementation of new clinical systems/processes.
  • Interface and collaborate with Investigators, IRBs/ECs, contractors/vendors, and company personnel as needed.

Administrative Tasks

  • Incumbent knows, understands, incorporates, and complies with all applicable laws and regulations relating to business activities, and Policies and Procedures of the Health Care Compliance Program and Code of Conduct.
  • May be asked to provide additional support to Clinical Operations staff, as needed.


  • A Bachelor Degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
  • Minimum 2 years experience in a CRA position.
  • Recent onsite clinical monitoring experience.
  • Fluency in Dutch and English (spoken and written).
  • Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products.
  • Relevant industry certifications preferred (i.e., CCRA, RAC, CDE).
  • Requires experience and knowledge working with computer systems (Microsoft Office - Excel, Word, and Power Point).
  • Leadership.
  • Written and verbal communication.
  • Presentation and influencing skills.
  • Strong organizational skills (e.g., able to manage multiple subprojects and tasks simultaneously and consistently meet all associated deadlines).
  • Ability to travel up to 80% of time : weekly travels to hospital sites in Belgium (mostly Flanders).
  • Full driving license.
  • Existing right to work in Europe required.


  • A balanced salary package based on your skills and experience, including extra legal benefits.
  • Full-time position