Clinical Trial Assistant / junior Clinical Research Associate M/V/X

Description de la fonction

We are looking for a motivated, detail-oriented Clinical Trial Assistant / Junior Clinical Research Associate to support clinical operations, monitoring activities, and patient engagement. This hybrid role combines structured operational work with scientific problem-solving and interaction with sites, patients, and healthcare professionals.

ResponsibilitiesClinical Operations Support

• Support day-to-day clinical trial activities from start-up to close-out.
• Prepare, review, and manage essential study documentation and TMF (inspection-ready).
• Track timelines, milestones, and deliverables.
• Coordinate communication with sites, sponsors, vendors, ethics committees, and HCPs.
• Support site visits, study meetings, contracting, invoicing, and investigator meetings.
• Assist with CTMS/eTMF systems.

Monitoring & Study Oversight

• Support on-site and remote monitoring under supervision.
• Review source data, CRFs, and essential documents for accuracy.
• Follow up on queries, deviations, and investigational product documentation.
• Apply ISO 14155 / ICH-GCP principles in daily work.

Patient Engagement Support

• Organize advisory boards, interviews, surveys, usability, and testing sessions.
• Coordinate logistics, scheduling, and materials for patient activities.
• Support patient interviews and communication in a structured and empathetic way.
• Document and report insights from patient engagement activities.
• Ensure all interactions reflect a respectful and high-quality patient experience.

Administrative & Office Support

• Provide general administrative and operational support.
• Assist with scheduling, onboarding, and internal documentation.
• Contribute to a well-organized and collaborative working environment.

Profil

Qualifications

• Master's degree in a scientific field preferred.
• Experience or strong interest in clinical research (through education, internships, or work).
• Knowledge of ISO 14155 / ICH-GCP, or willingness to learn.
• Strong organizational, communication, and computer skills (Microsoft Office).
• Accurate, proactive, and able to manage multiple tasks.
• Team player who can also work independently.
• Willingness to travel to study sites.
• Excellent command of English and Dutch; French is an asset.

Compétences linguistiques

• Anglais (atout)

  • Comprendre : Expérimenté - (C1)
  • Écrire : Expérimenté - (C1)
  • Lire : Expérimenté - (C1)
  • Parler : Expérimenté - (C1)

• Néérlandais (atout)

  • Comprendre : Expérimenté - (C1)
  • Écrire : Expérimenté - (C1)
  • Lire : Expérimenté - (C1)
  • Parler : Expérimenté - (C1)

• Français (atout)

  • Comprendre : Aucune connaissance
  • Écrire : Aucune connaissance
  • Lire : Aucune connaissance
  • Parler : Aucune connaissance

Avantages du poste

About JunipR Research

At JunipR Research, every interaction matters. We support life science companies through Clinical Operations, HCP and patient engagement, clinical strategy, and study committee management. We value scientific excellence, quality, respect, integrity, and collaboration.

As a Clinical Trial Assistant / Junior Clinical Research Associate, you will support clinical operations and monitoring activities, helping ensure studies run efficiently, data are reliable, and stakeholders receive professional, high-quality support.

Why Join JunipR Research?

JunipR is a growing company where talented people thrive. This role offers broad exposure to clinical operations, monitoring, and patient engagement, with clear development toward a CRA role.

At JunipR, you will:

• Support the delivery and growth of our clinical services.
• Gain experience across clinical studies and therapeutic areas.
• Learn best practices in clinical operations, monitoring, and patient involvement.
• Develop through hands-on experience and mentorship.
• Contribute to an excellent experience for patients, sites, HCPs, and sponsors.
• Work in a collaborative team focused on knowledge sharing.
• Benefit from a flexible Work From Home policy.
• Receive a competitive salary and benefits package.
• Grow in a culture that values quality, ownership, integrity, and continuous learning.

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