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Coloplast

Medical Affairs Program Manager

Minneapolis, MN, United States

$11.41 USD / hour

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Job details

Pay: $11.41 USD / hour
Experience: 5+ years' experience within clinical research and/or medical affairs activities, preferably with medical devices
Posting language: English
Posted: Oct 19, 2026

Original job description

Job Duties

Medical Affairs Program Manager

Location:

Minneapolis, MN, US

Job Family:

Research & Development

Country/Region:

United States

This position is a member of the Clinical Science & Office of Medical Affairs team. This role is responsible for driving and managing clinical documentation to support marketing and regulatory needs, supporting innovation and sustaining product activities, and providing clinical expertise as required. This position will comply with regulations and ensure clinical science & OMA activities comply with global regulatory requirements.

They will do this by defining near, medium and long-term objectives covering a broad range of medical affairs activities, such as:

Driving acceptance of Coloplast product claims in the clinical community through the generation of clinical evidence

Identifying external clinical opinions, perceptions and trends that influence Coloplast performance globally, and where warranted, develop appropriate mitigating strategies

Executing the scientific agenda, by engaging researchers through Coloplast activities and grants and other evidence generation activities

Supporting the development of any regulatory or quality associated documentation

Major Areas of Accountability

Serve as medical expert for relevant product(s) and associated clinical conditions

Oversee the medical affairs strategy development and implementation for designated area(s)

Support the required clinical input into documents including, but not limited to, instructions for use (IFUs), post-market clinical plans (PMCF), clinical evaluation reports (CERs), and other relevant documents

Support development and updates of Clinical Evaluation Reports (CERs) and associated documents as assigned (i.e. CER, PMCF, SSCP, PSUR, etc.)

Develop and deliver medical device technical documents supporting product launch and sustaining activities

Leverage latest literature, regulations and guidance to build and execute on evidence strategies

Drive publications of data to ensure relevant content at medical congresses and at Coloplast events.

Develop and deliver relevant medical device training documents (e.g. training decks, in-service scripts, eLearning tools, etc.) supporting product launch and sustaining activities

Supports with relevant medical writing expertise for evidence generation (e.g. white papers, clinical studies, publication plans, etc.).

Manage publication activities, as applicable

Develop/sustain knowledge in urology, including professional conference attendance

Support Investigator Initiated Study Program (IISP) as assigned

Process and review clinical study data using Good Clinical Practices (GCP) data-handling procedures and guidelines.

Support to medical marketing activities (KOL engagements, symposia, review/validation of communications)

Ensure timelines and milestones are achieved for all initiatives. Communicate regularly with stakeholders on project progress and risks to achieving milestones

Receive, provide, and track status updates from necessary stakeholders of assigned projects, ensuring alignment

Provides medical expertise for novel ideas, questions and information requests related to Interventional Urology products

Facilitates medical advisory boards and field-based KOL engagements as applicable

Ensures resources/time spent is in line with project prioritization

Participate in benefit/risk ratio assessment for vigilance and Risk Management Files

Coloplast employees are required to conduct business to the highest ethical and professional standards; comply with applicable laws and regulations, the MedTech Code of Conduct, and company policies.

Other duties as assigned

Basic Qualifications

Bachelor's degree in health science, engineering, or biotech area. Advanced degree in the health or engineering sciences preferred (MS, PhD, PharmD, MD)

5+ years' experience within clinical research and/or medical affairs activities, preferably with medical devices

Knowledge of and experience with ISO 14155, FDA, GCP, and MDR regulations

Ability to travel - 15-25%

Required Knowledge, Skills and Abilities

Strong ability to review and interpret scientific data and research and translate it for use cross-functionally

Demonstrated ability to work across functions to prioritize and drive strategic objectives

Excellent oral and written communication skills

Excellent project management and organizational skills

An understanding of engineering, biostatistics and trial design

High degree of initiative and self-motivation with a strong sense of accountability

Ability to identify, analyze and solve problems with minimal direction and make decisions with confidence

Aptitude to successfully prioritize and manage multiple tasks while adhering to deadlines

Adaptability to realign initiatives quickly to meet shifts in the market

Microsoft Word, Excel, PowerPoint proficiency required

Additional Responsibilities

Maintains strong understanding of product knowledge, relevant anatomy, and accepted applications and uses associated with our products

Develop mechanisms for monitoring project progress for timely intervention and problem solving

Present to, and partner with, business leaders on the overall health of the portfolio, successes, and areas of opportunity

Maintain awareness and understanding of the market and competitive space

At Coloplast, we believe in recognizing and rewarding the contributions of our employees. Our total rewards package is designed to support your well-being, foster your professional growth, and ensure a healthy work-life balance. Here is some of what you can expect:

Health and Wellness:Comprehensive medical, dental, and vision insurance plans to keep you and your family healthy. Plus, access to company sponsored wellness programs and mental health resources, paid leave of absence for qualifying events and generous paid parental leave for both birthing and non-birthing parents.

Financial Security:A competitive 401(k) plan with company match that vest immediately, financial planning services to help you secure your future, and corporate discount programs for goods and services.

Work-Life Balance:Generous paid time off, flexible work hours, and flexible work arrangement options to help you balance your personal and professional life may be available.

Professional Development:Opportunities for continuous learning and career advancement through training programs, mentorship, and tuition reimbursement.

Recognition and Rewards:Recognition programs to celebrate achievements and contributions, including peer recognition, bonuses, awards, and special events.

Community and Culture:A supportive work environment where everyone feels valued, and has a sense of belonging. Participate in team-building activities, volunteer opportunities, and company-sponsored events. Sustainability strategy that outlines our ambitions for how to run our company in a more sustainable way.

Competitive Compensation: The compensation range for this position is $108,000 - $150,000. Actual compensation is influenced by a variety of factors including but not limited to skills, experience, qualifications, and geographic location. Hired candidates may be eligible to receive additional compensation in the form of bonuses and/or incentives.

Pursuing an ambitious growth agenda, 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 worlds 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.

Visit us onColoplast.com.

Watch the film.Follow us onLinkedIn.

Coloplast employees are required to conduct business to the highest ethical and professional standards; comply with applicable laws and regulations, the Advamed Code of Ethics on Interactions with Healthcare Professionals, and company policies.

Coloplast is committed to a policy of Equal Employment Opportunity (EEO) which means we employ and promote individuals based on their merits, regardless of race, color, religion, sex, national origin, age, disability, veteran status, pregnancy, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, status with regards to public assistance or any other protected classification.

62303

Nearest Major Market: Minneapolis

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EOE M/W/Vets/Disabled

Minimum Education Required

Bachelor Degree

Minimum Experience Required

5 - 20 years

Shift

First (Day)

Number of Openings

Public Transportation Accessible

Yes

Veterans Encouraged to Apply

Physical Required

Yes

Drug Test Required

Yes

Compensation

$11.41 / Hourly

Postal Code

55411

Job Type

Full Time

Place of Work

On-site

Requisition ID

62303

Job Benefits

Not specified

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