Clinical Trials Associate Manager (1-Year Fixed-Term)

Coloplast; Humlebæk; Remote; DKK 650,000 - 820,000; Full time

Job summary

Coloplast is seeking an Associate Clinical Manager for a one-year fixed-term position in Humlebæk, Denmark. You will participate in planning, managing, and executing clinical investigations for our medical devices portfolio, collaborating with external healthcare professionals and hospital departments.

You will contribute to investigation plans, budget forecasting, site identification, investigator qualification, and training, while supporting regulatory approvals and ethics submissions.

Qualifications

• Experience with clinical trials and strong stakeholder management skills
• Hold a degree within life sciences, applied sciences, nursing or similar
• Have experience with clinical investigations of medical devices or pharmaceuticals
• Are familiar with the guidelines and directives within clinical research
• Possess project management proficiency and can stay on budget
• You are fluent in spoken and written English

Responsibilities

• Contribute to the development of clinical investigation plans and study-related materials and assist with budget forecasting
• Support site identification, investigator qualification, selection, and training activities
• Support the process of obtaining approvals from health authorities and ethics committees
• Assist in monitoring and coordinating field monitors and contract research organisations
• Help ensure patient recruitment remains on track
• Prepare, maintain, and archive sponsor and investigator site files
• Support the planning and oversight of study material packaging to maintain accountability throughout the investigation

Skills

Stakeholder management

Project management

Budget management

English proficiency

Education

Life sciences or nursing degree

Job description

Coloplast is seeking an Associate Clinical Manager for a one-year fixed-term position in Humlebæk, Denmark. You will participate in planning, managing, and executing clinical investigations for our medical devices portfolio, collaborating with external healthcare professionals and hospital departments.

You will contribute to investigation plans, budget forecasting, site identification, investigator qualification, and training, while supporting regulatory approvals and ethics submissions.