Clinical Project Manager (MedTech, Copenhagen)

Job summary

This role involves managing clinical investigations and surveys within the MedTech sector, focusing on innovative dental diagnostic solutions. The position is a maternity cover and requires collaboration with various internal and external stakeholders to ensure compliance and successful project delivery.

Qualifications

• Master’s degree in a scientific field; PhD preferred
• Experience in managing clinical studies in the medical device industry
• Strong knowledge of EU MDR, ISO 14155, and Good Clinical Practice (GCP); certification is a plus
• Relevant experience in clinical operations and medical/scientific writing
• Familiarity with post-market clinical follow-up (PMCF)
• Excellent organizational and communication skills
• Fluent in written and spoken English

Responsibilities

• Lead planning, execution, and delivery of clinical investigations in compliance with regulations
• Manage clinical documentation including study protocols, consent forms, and reports
• Oversee study timelines, budgets, and resources
• Provide methodological support for clinical investigations
• Ensure adherence to regulatory and ethical standards
• Collaborate with internal teams and external partners
• Assist during internal and external audits

Skills

• Strong interpersonal skills and ability to work with diverse stakeholders
• Ability to manage multiple projects and meet tight deadlines

Education

• Master’s degree in a scientific field, PhD preferred

Tools

• Familiarity with clinical trial management systems and regulatory compliance tools