GlaxoSmithKline GmbH & Co. KG
Senior Heme Clinical Trial RMAM(m/w/x)
Full-timeOn-siteSenior
München
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GLGlaxoSmithKline GmbH & Co. KG
Heme Clinical Trial RMAM(m/w/x)
München
Full-timeOn-siteExperienced
Nejo AI Summary
Coordinating local medical research activities for biopharma, ensuring scientific and operational quality. Advanced degree and 3+ years in medical affairs or clinical research required. Regular regional travel, German and English fluency.
Requirements
- Advanced degree in medicine, pharmacy, life sciences or related field
- At least 3 years' experience in medical affairs, medical science liaison, clinical research or related industry role
- Strong clinical and scientific knowledge relevant to therapy area
- Excellent verbal and written communication skills in German and English
- Willingness and ability to travel regularly within assigned region
- Solid understanding of regulatory, ethical, and compliance requirements in pharmaceutical environment
- Prior experience in oncology, hematology or related therapy areas
- Experience supporting investigator-initiated trials or clinical partnerships
- Experience designing or delivering omnichannel engagement plans and digital medical communications
- Project management or budget management experience
- Experience presenting at national or regional scientific meetings
- Collaborative mindset and commitment to inclusive working with diverse stakeholders
Tasks
- Lead and coordinate local medical research activities
- Ensure high scientific and operational quality
- Plan clinical studies in line with regulatory standards
- Execute clinical studies in line with regulatory standards
- Communicate clinical studies in line with regulatory standards
- Manage internal partners for quality, timelines, and budget
- Manage external partners for quality, timelines, and budget
- Act as a central interface for local and global Medical Affairs
- Liaise with regional medical affairs managers
- Liaise with clinical development teams
- Liaise with clinical research organizations
- Ensure cross-functional collaboration
- Plan regional medical activities
- Run regional medical activities
- Contribute to generating high-impact data in clinical trials
- Contribute to generating robust data in clinical trials
Work Experience
- 3 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of GlaxoSmithKline GmbH & Co. KG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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GLGlaxoSmithKline GmbH & Co. KG
Heme Clinical Trial RMAM(m/w/x)
München
Full-timeOn-siteExperienced
Nejo AI Summary
Coordinating local medical research activities for biopharma, ensuring scientific and operational quality. Advanced degree and 3+ years in medical affairs or clinical research required. Regular regional travel, German and English fluency.
Requirements
- Advanced degree in medicine, pharmacy, life sciences or related field
- At least 3 years' experience in medical affairs, medical science liaison, clinical research or related industry role
- Strong clinical and scientific knowledge relevant to therapy area
- Excellent verbal and written communication skills in German and English
- Willingness and ability to travel regularly within assigned region
- Solid understanding of regulatory, ethical, and compliance requirements in pharmaceutical environment
- Prior experience in oncology, hematology or related therapy areas
- Experience supporting investigator-initiated trials or clinical partnerships
- Experience designing or delivering omnichannel engagement plans and digital medical communications
- Project management or budget management experience
- Experience presenting at national or regional scientific meetings
- Collaborative mindset and commitment to inclusive working with diverse stakeholders
Tasks
- Lead and coordinate local medical research activities
- Ensure high scientific and operational quality
- Plan clinical studies in line with regulatory standards
- Execute clinical studies in line with regulatory standards
- Communicate clinical studies in line with regulatory standards
- Manage internal partners for quality, timelines, and budget
- Manage external partners for quality, timelines, and budget
- Act as a central interface for local and global Medical Affairs
- Liaise with regional medical affairs managers
- Liaise with clinical development teams
- Liaise with clinical research organizations
- Ensure cross-functional collaboration
- Plan regional medical activities
- Run regional medical activities
- Contribute to generating high-impact data in clinical trials
- Contribute to generating robust data in clinical trials
Work Experience
- 3 years
Education
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of GlaxoSmithKline GmbH & Co. KG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
GlaxoSmithKline GmbH & Co. KG
Industry
Pharmaceuticals
Description
GSK is a global biopharma company uniting science, technology and talent to get ahead of disease. They focus on specialty medicines and vaccines in respiratory, immunology, oncology, HIV, and infectious diseases.
Not a perfect match?
- GlaxoSmithKline GmbH & Co. KG
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Full-timeOn-siteSeniorMünchen - GlaxoSmithKline GmbH & Co. KG
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