eCOA Project Manager – Clinical Trials Solutions

medable; Denmark; On-site; DKK 850,000 - 1,400,000; Full time

Job summary

Medable is seeking an experienced Project Manager to lead end-to-end software implementation in clinical trials, spanning from kickoff to go-live and localizations. You will work with design teams to interpret trial requirements and manage scope, timelines, and budgets while ensuring regulatory compliance.

Lead cross-functional collaboration, drive change management, and deliver robust, scalable solutions with a focus on client communication and successful deployments across European studies.

Qualifications

• Minimum of 6 years of experience or equivalent combination of education and experience.
• Proven experience in managing full lifecycle software implementation projects.
• Advanced proficiency in change management and coordinating cross-functional teams.
• Extensive experience supporting in-flight projects with adaptive approaches.
• Strong knowledge of clinical trial domains and regulatory compliance.

Responsibilities

• Manage the initial deployment lifecycle of the Medable Solution from kick-off through go-live.
• Collaborate with solution design teams to understand trial-specific requirements.
• Oversee project scope, timelines and budgets, including timecards and budget adherence.
• Align System Specifications with clinical trial protocols and schedules.
• Develop adaptive project plans to incorporate evolving client needs.
• Educate clients and internal teams on software capabilities and best practices.

Skills

Project management

Cross-functional leadership

Communication skills

Change management

Strategic planning

Education

Bachelor's degree in Computer Science, Health Informatics, or related field

Master's degree in Computer Science, Health Informatics, or relevant domain (preferred)

Project Management Professional (PMP) / PRINCE2 or equivalent

Job description

Medable is seeking an experienced Project Manager to lead end-to-end software implementation in clinical trials, spanning from kickoff to go-live and localizations. You will work with design teams to interpret trial requirements and manage scope, timelines, and budgets while ensuring regulatory compliance.

Lead cross-functional collaboration, drive change management, and deliver robust, scalable solutions with a focus on client communication and successful deployments across European studies.