Medical Manager CRM

WHO ARE WE?

Boehringer Ingelheim Sweden is research-driven, family-owned company committed to delivering innovative health solutions that improve lives. As part of the Regional Operating Unit MIDI, covering Belgium, Denmark, Finland, Greece, Norway, Portugal, Sweden, and The Netherlands, we thrive in a multicultural and diverse environment with more than 1,800 employees working together to advance science and patient care.

THE OPPORTUNITY

Join our passionate Medical Affairs team in Stockholm and help shape the future of cardio-renal-metabolic (CRM) treatment in Sweden. As Medical Manager CRM, you will lead medical strategy and execution for one of our products within the CRM area. You will ensure scientific excellence and compliance while collaborating with cross-functional teams to support product lifecycle management, regulatory requirements, and market access.

Also, you will be the face of Boehringer Ingelheim to high-level scientific professionals where you will engage in scientific discussions and idea exchange, where the ultimate goal is to ensure that the right patients are treated optimally with a focus on new scientific approaches.

You will report directly to the Medical Affairs Team Lead CRM and work closely with the colleagues in the Medical Affairs team, as well as with Marketing, Sales, Market Access, Regulatory Affairs, Pharmacovigilance, and Clinical Operations.

This position is based in Stockholm (Hammarby Sjöstad) and includes traveling within Sweden and internationally.

This is a fantastic opportunity for an experienced professional who wants to be part of a truly innovative and revolutionary team! Join us if you want to make a difference. 

YOUR KEY RESPONSIBILITIES

• Drive medical initiatives and projects within the CRM therapeutic area, leveraging your expertise to support product lifecycle management.


• Develop and maintain strong relationships with External Experts (EEs), healthcare professionals, authorities, and patient organizations.


• Provide scientific and strategic input to asset teams and contribute to the development of local plans.


• Ensure compliance with local and global regulatory and ethical standards.


• Lead, and support clinical and scientific projects, including investigator-initiated studies, real-world evidence generation, and implementation trials.


• Develop medical educational content for external and internal stakeholders.


• Deliver medical training and support to internal teams, including field force training.


• Gather and analyze medical insights to inform strategy and decision-making.


• Act as a scientific partner in cross-functional teams and contribute to product lifecycle management (pre-launch, launch, post-launch)

WHAT YOU SHOULD BRING TO THE TEAM

• Medical Doctor’s degree is strongly preferred, alternatively Master’s/PhD in Medicine, Pharmacy, or Life Sciences.


• At least 5 years previous experience within CRM therapeutic areas, gained in the pharmaceutical industry, academia, or healthcare sector.


• Strong understanding of the Swedish healthcare system and regulatory environment.


• Excellent command of English and Swedish.


• Strategic mindset with strong business acumen.


• Excellent communication and presentation skills.


• Proven ability to manage complex projects and drive change.


• Collaborative team player with experience in cross-functional environments.

WHAT WILL YOU GET IN RETURN?

• Work in a research-driven, wellbeing-oriented organization that values innovation and employee health.


• Pleasant and informal working atmosphere.


• Flexible working hours and possibility to work from home office 1-2 days/week.


• Customized development plan based on your role and aspirations


• Competitive salary range and health insurance 

What’s next?

Please submit your CV and Motivation Letter in Swedish or in English.

Application deadline: 14 February 2026. We encourage you to apply early! We will review your application and, if there’s a match, invite you for an interview to get to know each other. We’ll keep you informed throughout the process.

Screening:

In order to comply with applicable export control laws, Boehringer Ingelheim periodically screens business relations (including job applicants) against sanctioned party lists (“SPL”). These checks may be performed by Boehringer Ingelheim or by any of its Affiliates. You acknowledge that Boehringer Ingelheim and/or its Affiliates will screen you against SPL and that for this purpose your personal data may be processed in relevant databases, including databases of third-party vendors that perform SPL screening for or on behalf of Boehringer Ingelheim or its Affiliates which may be located or accessible outside the EU. Boehringer Ingelheim is committed to ensuring an adequate level of protection of your personal data.