Consultant Assignment: Clinical Trial Coordinator

We are now seeking an experienced Clinical Trial Coordinator to support one of our client's upcoming Phase III clinical study in Europe (approx. 100 participants, 1‑year duration). Hybrid role based in Sweden Occasional travel to clinical sites and CRO meetings

Key Responsibilities

• Coordinate communication and operational activities between the sponsor, CRO, and clinical sites
• Support study startup, site onboarding, and performance oversight
• Ensure compliance with protocols, timelines, and ICH‑GCP
• Maintain high‑quality documentation and cross‑functional alignment

Qualifications

• Bachelor’s degree in life sciences
• 4+ years’ experience in clinical research, ideally Phase II-III
• Strong knowledge of GCP and multi‑site trial operations
• Excellent communication and organizational skills

Competency Profile

• Regulatory & Quality: Solid understanding of ICH‑GCP and protocol compliance
• Operational Skills: Experience with EDC, CTMS, and eTMF systems
• Stakeholder Management: Skilled at liaising with CROs, investigators, and internal teams
• Data & Documentation: Accurate, detail‑oriented, and quality‑driven
• Coordination & Planning: Able to manage timelines, tasks, and study logistics effectively