Phase 1 Clinical Trial Manager – Denmark (SCRA)

Syneos Health Denmark ApS; Denmark; Remote; DKK 520,000 - 780,000; Full time

Job summary

Syneos Health Denmark ApS is seeking a Clinical Trial Manager or SCRA (Sponsor Dedicated) in Denmark. You will lead Phase 1 studies, ensure GCP/regulatory compliance, and collaborate with investigators, client teams and clinic operations to drive study success.

The role requires 3+ years in clinical trial management, strong project and communication skills, and proficiency with CTMS/EDC systems. You will support multiple projects and help mentor team members in a fast-paced environment.

Qualifications

• Bachelor's degree in life sciences, clinical research or related field.
• Minimum 3 years of experience in clinical trial management.
• Knowledge of clinical research processes and regulations.
• Strong project management and organizational skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency with clinical trial management software and tools.

Responsibilities

• Develop and coordinate Phase 1 clinical studies with meticulous planning.
• Implement protocols and ensure regulatory compliance (GCP).
• Collaborate with investigators, clients and clinic teams.
• Plan logistics, budgeting and resource allocation for trials.
• Track progress and report milestones to stakeholders.
• Prepare study reports and data analyses for reviews.
• Ensure adherence to global/regional regulations and updates.
• Provide guidance to junior staff and foster teamwork.
• Maintain rigorous study documentation.

Skills

Project management

Communication

GCP knowledge

Microsoft Office

Teamwork

Independence

Education

Bachelor's degree in life sciences or clinical research

Tools

CTMS

EDC systems

Job description

Syneos Health Denmark ApS is seeking a Clinical Trial Manager or SCRA (Sponsor Dedicated) in Denmark. You will lead Phase 1 studies, ensure GCP/regulatory compliance, and collaborate with investigators, client teams and clinic operations to drive study success.

The role requires 3+ years in clinical trial management, strong project and communication skills, and proficiency with CTMS/EDC systems. You will support multiple projects and help mentor team members in a fast-paced environment.