Associate Clinical Manager (One-Year Fixed-Term Position)

Coloplast; Humlebæk; On-site; 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

Associate Clinical Manager (One-Year Fixed-Term Position)

Location: Humlebæk, DK

Job Family: Research & Development

Would you like to plan and execute clinical studies for a market leader within the medical device industry? And do you want to provide evidence to support products that make a real difference to people with intimate health care needs?

Become part of a specialist community At our HQ in Humlebæk, you will join 9 colleagues in the Clinical Execution team in Clinical & Medical Affairs - Payers & Evidence.
We plan and execute clinical investigations within our Chronic Care and Wound Care portfolio.

Ensure the optimal clinical investigations As an Associate Clinical Manager, you will, under guidance, take part in the planning, management, and execution of clinical investigations, becoming involved in the entire process from study start to completion.

To facilitate studies, you will collaborate and build great working relationships with relevant external health care professionals and hospital departments. Ultimately, your work will help provide some of the solutions doctors and nurses need to deliver the best possible care and treatment.

More specifically, you will:

• 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

You should expect approximately 20 travel days per year to monitor studies, visit hospitals and consult with medical staff both in Denmark and internationally.

Experience with clinical trials and strong stakeholder management skills

What you bring:

• 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

As you gradually take on increasing responsibility within clinical investigations, it is important that you have a structured approach to your work and the ability to keep activities moving forward.

Your strong interpersonal skills help you build relationships and collaborate effectively with colleagues, investigators, and external partners.

Coloplast develops and markets products and services that make life easier for people with intimate healthcare needs. Employing about 16.000 people and with products available in more than 143 countries, we are one of the world´s leading medical device companies. We are constantly growing our business and always looking for new ways to move forward – we explore, learn and look for new ways of doing things.

Coloplast is committed to being an inclusive organization, where people bring their differences to work each day, fulfil their potential and have a strong sense of belonging because – and not despite – of their differences. We therefore encourage all qualified candidates to apply regardless of gender, age, race, nationality, ethnicity, sexual orientation, religious belief or physical ability.

Coloplast Group - Holtedam 1 - Humlebaek - DK 3050 - Denmark