Remote Clinical Trial Coordinator – Denmark

MSD

København

Remote

DKK 480,000 - 640,000

Full time

4 days ago
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Job summary

Innovate and Deliver is seeking a Clinical Trial Coordinator in Denmark to act as the operational heartbeat of multi-country studies. You will manage site readiness, document control, and systems across the CTMS/eTMF landscape.

The role requires a life sciences background, experience in clinical research, and fluency in English and Danish. You will collaborate with COM/CRM/CRA and site teams to ensure timely milestones and regulatory compliance.

Qualifications

  • Bachelor’s degree or equivalent training in life sciences, healthcare or admin.
  • Experience in a clinical research environment with drug development knowledge.
  • Familiarity with ICH‑GCP and Good Documentation Practices.

Responsibilities

  • Drive trial and site administration across the Denmark cluster.
  • Coordinate site readiness and provisioning with internal and external stakeholders.
  • Manage logistics for clinical/non-clinical supplies, labeling, and translations.
  • Track essential documents and safety updates to maintain data integrity.
  • Operate CTMS, eTMF and related clinical systems.
  • Prepare, archive, and reconcile eTMF content for inspection readiness.
  • Assist in regulatory submissions and startup activities.
  • Support budgets, contracts, and payments.

Skills

Clinical Data Management
Clinical Development
Clinical Documentation
Clinical Research
GCP/ICH GCP
Cross‑functional collaboration
Communication in English & Danish

Education

Bachelor's degree in life sciences or related field

Tools

CTMS
eTMF

Job description

Innovate and Deliver is seeking a Clinical Trial Coordinator in Denmark to act as the operational heartbeat of multi-country studies. You will manage site readiness, document control, and systems across the CTMS/eTMF landscape.

The role requires a life sciences background, experience in clinical research, and fluency in English and Danish. You will collaborate with COM/CRM/CRA and site teams to ensure timely milestones and regulatory compliance.

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