Clinical trial associate

Clinical Trial Associate (CTA) – Dermatology

Belgium (Remote) | Full-Time

About the Role

We're seeking a detail-oriented Clinical Trial Associate (CTA) to support the execution of dermatology clinical trials. Working closely with Clinical Operations, Regulatory Affairs, CROs, and investigator sites, you will play a key role in ensuring studies are delivered efficiently and in compliance with ICH-GCP and regulatory requirements.

Key Responsibilities

• Support study start-up, maintenance, and close-out activities.
• Maintain Trial Master Files (TMF/eTMF) and ensure inspection readiness.
• Track study timelines, milestones, and study documentation.
• Coordinate investigator site communications and essential document collection.
• Support CRO and vendor management activities.
• Organize study team meetings and training sessions.
• Maintain study trackers, reports, and operational metrics.
• Ensure compliance with SOPs, ICH-GCP, and applicable regulations.

Qualifications

• Bachelor's degree in Life Sciences or a related field.
• 1–3 years of experience in Clinical Operations, Clinical Research, or a Clinical Trial Associate role.
• Previous dermatology clinical trial experience is required.
• Strong understanding of ICH-GCP and clinical trial processes.
• Experience with TMF/eTMF management.
• Familiarity with CTMS, EDC, and other clinical trial systems is preferred.
• Experience within a biotech, pharmaceutical, or CRO environment is advantageous.
• Strong organizational, communication, and stakeholder management skills.
• Must be based in Belgium and have authorization to work in Belgium.

Please apply ASAP and I'll be in touch as CV's will be sent over to the biotech in 48 hours!!