The AI Job Search Engine
Team Lead - Clinical Affairs(m/w/x)
Leading global strategy for medical device clinical evaluation and regulatory compliance. Extensive experience in clinical research or medical device evaluation with international team leadership expected. 30 vacation days, flexible hybrid work.
Requirements
- Advanced scientific, medical, or technical degree
- Extensive clinical affairs or research experience
- Background in Class I–III medical devices
- Leadership experience managing international teams
- Experience in Clinical Affairs, Research, or R&D
- Clinical and regulatory background for medical devices
- Knowledge of EU MDR, FDA, and GCP
- Experience in clinical studies and evaluations
- Ability to translate research into marketing
- Stakeholder management and project leadership skills
- Understanding of GDPR and data protection
- Very good English and German skills
Tasks
- Define and lead the global Clinical Affairs strategy
- Align clinical goals with product and regulatory objectives
- Lead and develop an international Clinical Affairs team
- Oversee clinical evaluation and scientific marketing communication
- Ensure clinical compliance with EU MDR and FDA requirements
- Build networks with investigators and research partners
- Train authors and evaluators on regulatory compliance
- Translate clinical insights into product innovation
- Convert research evidence into high-impact educational content
- Ensure GDPR compliance in clinical collaborations
- Manage clinical studies to support regulatory approvals
- Represent the company in communications with regulatory authorities
Education
- Doctoral / PhD
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- EU MDR
- FDA regulations
- Good Clinical Practice
- GDPR
Benefits
Flexible Working
- Flexible working hours
- Hybrid work model
Informal Culture
- Mutually-supportive international team
Purpose-Driven Work
- Meaningful work
More Vacation Days
- 30 vacation days
- December 24th and 31st off
Company Bike
- Bike leasing
Parking & Commuter Benefits
- Parking garage
- Safe underground bike storage
Free or Subsidized Food
- Subsidized company restaurant
Snacks & Drinks
- In-house cafes
Healthcare & Fitness
- 360m2 company gym
- Fitness program
Team Events
- Regular after work events
- Team and company events
Learning & Development
- Comprehensive training
- Continuing education opportunities
Not a perfect match?
- Ipsen Pharma GmbHFull-timeWith HomeofficeSeniorMünchen
- Baxter Medical Systems GmbH + Co. KG
Senior Manager Medical Affairs(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - Denk Pharma GmbH & Co. KG
Teamlead International Regulatory Affairs(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - ImFusion GmbH
Senior Quality Management and Regulatory Affairs Manager(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - ARES Recruiting GmbH
Teamleiter Clinical Specialist TAVI(m/w/x)
Full-timeWith HomeofficeExperiencedMünchen
Team Lead - Clinical Affairs(m/w/x)
Leading global strategy for medical device clinical evaluation and regulatory compliance. Extensive experience in clinical research or medical device evaluation with international team leadership expected. 30 vacation days, flexible hybrid work.
Requirements
- Advanced scientific, medical, or technical degree
- Extensive clinical affairs or research experience
- Background in Class I–III medical devices
- Leadership experience managing international teams
- Experience in Clinical Affairs, Research, or R&D
- Clinical and regulatory background for medical devices
- Knowledge of EU MDR, FDA, and GCP
- Experience in clinical studies and evaluations
- Ability to translate research into marketing
- Stakeholder management and project leadership skills
- Understanding of GDPR and data protection
- Very good English and German skills
Tasks
- Define and lead the global Clinical Affairs strategy
- Align clinical goals with product and regulatory objectives
- Lead and develop an international Clinical Affairs team
- Oversee clinical evaluation and scientific marketing communication
- Ensure clinical compliance with EU MDR and FDA requirements
- Build networks with investigators and research partners
- Train authors and evaluators on regulatory compliance
- Translate clinical insights into product innovation
- Convert research evidence into high-impact educational content
- Ensure GDPR compliance in clinical collaborations
- Manage clinical studies to support regulatory approvals
- Represent the company in communications with regulatory authorities
Education
- Doctoral / PhD
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- EU MDR
- FDA regulations
- Good Clinical Practice
- GDPR
Benefits
Flexible Working
- Flexible working hours
- Hybrid work model
Informal Culture
- Mutually-supportive international team
Purpose-Driven Work
- Meaningful work
More Vacation Days
- 30 vacation days
- December 24th and 31st off
Company Bike
- Bike leasing
Parking & Commuter Benefits
- Parking garage
- Safe underground bike storage
Free or Subsidized Food
- Subsidized company restaurant
Snacks & Drinks
- In-house cafes
Healthcare & Fitness
- 360m2 company gym
- Fitness program
Team Events
- Regular after work events
- Team and company events
Learning & Development
- Comprehensive training
- Continuing education opportunities
About the Company
Brainlab
Industry
Healthcare
Description
The company develops, manufactures and markets software-driven medical technology, enabling access to improved, more efficient, less-invasive patient treatments.
Not a perfect match?
- Ipsen Pharma GmbH
Senior Medical Lead - New Launches(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - Baxter Medical Systems GmbH + Co. KG
Senior Manager Medical Affairs(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - Denk Pharma GmbH & Co. KG
Teamlead International Regulatory Affairs(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - ImFusion GmbH
Senior Quality Management and Regulatory Affairs Manager(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - ARES Recruiting GmbH
Teamleiter Clinical Specialist TAVI(m/w/x)
Full-timeWith HomeofficeExperiencedMünchen