Remote Clinical Trial Coordinator | Danish Ops

MSD Malaysia; København; Hybrid; DKK 420,000 - 660,000; Full time

Job summary

Merck & Co., Inc. in Denmark seeks a Clinical Trial Coordinator to ensure site readiness, manage CTMS/eTMF, and support regulatory submissions across a multi-country cluster.

You will coordinate site readiness, manage documents, and assist with budgets and payments while collaborating with COM, CRM, CRA, and study sites.

This role requires a life sciences degree, clinical research experience, and fluency in English and Danish with a proactive, detail-oriented mindset.

Qualifications

• Bachelor's degree in life sciences or related field, or equivalent training.
• Experience in a clinical research environment with knowledge of drug development.
• Knowledge of ICH-GCP, Good Documentation Practices, and applicable regulations.
• Fluent in English and Danish.

Responsibilities

• Drive trial and site administration, ensuring site readiness and regulatory compliance.
• Coordinate country/site document collection for validation, start-up, and submissions; manage regulatory submissions.
• Oversee CTMS, eTMF, and related systems; ensure inspection readiness and document translations.

Skills

Clinical Trials Coordination

Regulatory Compliance

CTMS/eTMF Management

Cross-functional Collaboration

Data Integrity

Education

Bachelor's degree in life sciences or related field

Tools

CTMS

eTMF

Job description

Merck & Co., Inc. in Denmark seeks a Clinical Trial Coordinator to ensure site readiness, manage CTMS/eTMF, and support regulatory submissions across a multi-country cluster.

You will coordinate site readiness, manage documents, and assist with budgets and payments while collaborating with COM, CRM, CRA, and study sites.

This role requires a life sciences degree, clinical research experience, and fluency in English and Danish with a proactive, detail-oriented mindset.