Clinical Trial Coordinator

Job Description

Clinical Trial Coordinator (CTC) — Denmark | Innovate and Deliver

Application deadline is 23rd October.

Across Borders

Make a real impact on patients’ lives by powering high-quality, compliant clinical trials across a multi-country cluster. We’re seeking a detail-driven, tech-savvy Clinical Trial Coordinator (CTC) based in Denmark to be the operational heartbeat of our studies—keeping sites moving, documents inspection-ready, and ensuring study files and systems are up to date.

Operating at a cluster level, you’ll be the central connector for Clinical Operations Managers (COM), Clinical Research Managers (CRM), Clinical Research Associates (CRA), and study sites across multiple countries. Your work ensures site readiness, regulatory compliance (including ICH-GCP), and on-time delivery of trial milestones.

What you’ll do

• Drive trial and site administration
  • 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
  • Confidently manage Clinical Trial Management Systems (CTMS), electronic Trial Master Files (eTMF), and related clinical systems
• Own document excellence
  • Prepare, archive, and reconcile eTMF content for inspection readiness
  • Execute quality control plans and manage document translations
  • Maintain investigator site file binders and supply destruction records
• Accelerate regulatory submissions and start-up
  • Coordinate country/site document collection for validation, start-up, and submissions
  • Support IRB/IEC and regulatory submissions and track insurance certificates
  • Ensure publication of study results in line with local legislation
• Support budgets, contracts, and payments
  • Assist in the development of site budgets, contracts, and handle payment execution.
  • Ensure compliance with financial procedures
• Orchestrate meetings
  • Organize meetings such as study and investigator events.

What you’ll bring

• Education and experience
  • Bachelor’s degree preferred (life sciences/health-related field) or training in office management, administration, finance, or healthcare
  • Experience in a clinical research environment with solid understanding of drug development
  • Knowledge of ICH-GCP, Good Documentation Practices, and applicable regulations
• Communication and collaboration
  • Fluent in English and Danish
  • Proven success working independently and in cross-functional, multicultural, global/matrix teams
  • Positive mindset
• Professional behaviors
  • Prioritizes effectively and delivers on time, with meticulous attention to detail
  • Stays resilient and adaptable, managing shifting priorities
  • Communicates clearly and respectfully; navigates negotiations and stakeholder alignment with confidence
  • Identifies issues early and solves them analytically, using data and sound judgment
  • Operates fluently in CTMS, eTMF, and core digital tools; learns new systems quickly
  • Drives continuous improvement—simplifies processes, removes friction, and standardizes where possible
  • Maintains accountability for quality and timelines, following through reliably
  • Demonstrates a growth mindset—shares knowledge, seeks feedback, and embraces learning
  • Challenges the status quo thoughtfully, leveraging digital tools to innovate and improve outcomes

We are a company that values teamwork, innovation, and personal development. We offer a dynamic and international work environment where you will have the opportunity to grow and develop your skills while contributing to meaningful research.

If you are interested in this position, please submit your application. We look forward to hearing from you!

Required Skills:

Clinical Data Management, Clinical Development, Clinical Documentation, Clinical Research, Clinical Trial Compliance, Clinical Trial Documentation, Clinical Trial Management, Clinical Trials Monitoring, Clinical Trials Operations, Clinical Trial Support, Good Clinical Practice (GCP), ICH GCP Guidelines, On Site Monitoring, Research Designs, Site Initiation, Status Reporting, Study Design, Task Management

Preferred Skills:

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Search Firm Representatives Please Read Carefully 
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Remote

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

10/24/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.