Associate Medical Director - Remote

SOLVENTUM•Remote - Minnesota, MN

3d•$143,200 - $196,900•Remote

About The Position

Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges. The Impact You’ll Make in this Role: Provide medical insights for product development, risk assessments, and customer interactions. Oversee the design, execution, and analysis of clinical studies to support product approvals and post-market surveillance. Medical monitoring during clinical trials by reviewing safety data, assessing adverse events, and ensuring participant safety throughout the study. Provide medical expertise in complaint management. Develop and maintain relationships with key opinion leaders and industry experts to gather insights. Collaborate closely with R&D, Quality Assurance, Regulatory Affairs, and Marketing teams to align clinical objectives with business goals. Ensure compliance with all relevant regulatory requirements and guidelines. Contribute to the training of medical and non-medical personnel. Provide medical input for the development of marketing and educational materials. Support the development and execution of medical education and scientific evidence strategies.

Requirements

MD or equivalent medical degree
A minimum of 5 years of clinical experience.
Experience in a medical affairs role within the medical device industry.
General, working knowledge of statistical principles, Good Clinical Practice concepts, and other regulations and standard practices governing clinical research, including medical monitoring.
Lead cross-functional teams and manage complex projects.
Deliver clear, accurate written and verbal communications when presenting complex information to stakeholders.
Experience applying established processes/procedures to resolve work-related issues.
Manage shifting priorities and complete work effectively in a fast‑paced environment.
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

Nice To Haves

Familiarity with medical device regulations.
Advanced postgraduate qualifications in a relevant field like medicine, Management, etc.
Active registration.
Proficiency in additional languages is an advantage.

Responsibilities

Provide medical insights for product development, risk assessments, and customer interactions.
Oversee the design, execution, and analysis of clinical studies to support product approvals and post-market surveillance.
Medical monitoring during clinical trials by reviewing safety data, assessing adverse events, and ensuring participant safety throughout the study.
Provide medical expertise in complaint management.
Develop and maintain relationships with key opinion leaders and industry experts to gather insights.
Collaborate closely with R&D, Quality Assurance, Regulatory Affairs, and Marketing teams to align clinical objectives with business goals.
Ensure compliance with all relevant regulatory requirements and guidelines.
Contribute to the training of medical and non-medical personnel.
Provide medical input for the development of marketing and educational materials.
Support the development and execution of medical education and scientific evidence strategies.
Ensure compliance with corporate policies, procedures and security standards while performing assigned duties.