18 Jobs für Medical Affairs Communicator
Stellenangebote Medical Affairs Communicator Jobs
Job vor 4 Tagen bei Stellenanzeigen.de gefunden
GYNEMED GmbH Co. KG
• Schleswig- Holstein 23730
Homeoffice möglich
We are seeking an experienced and proactive Regulatory
Affairs Specialist to join our international team and strengthen our global regulatory and quality management activities. In this role, you will be [...]
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[...] responsible for driving regulatory strategies and submissions not only in Europe (MDR) and the U. S. (FDA) , but also across diverse international markets. By ensuring compliance with global [. .. ] fertility care by ensuring our products meet highest quality standards and global regulatory requirements. The position is based at our German subsidiary near Lübeck. Regulatory Affairs Specialist (m/f/d) Medical Devices (Full-time) Your tasks Lead and support cross-functional projects in regulatory affairs and quality management. Identify, interpret, and implement regulatory requirements across global markets, with a strong focus on international registrations outside the U. S. and EU. Independently prepare submissions and change notifications for competent authorities and international [. .. ] across diverse geographies. Independent, structured, and detail-oriented way of working combined with a collaborative mindset. Fluency in German and English; additional languages are an advantage for international registrations. Confident communicator with the ability to build strong internal and external relationships. Proficiency in MS Office applications. We offer An exciting and varied role in a collaborative, international environment. Direct involvement in global registration strategies, with significant responsibility for markets outside the EU and U. S. Flat hierarchies and the opportunity to [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] scientific, regulatory, and industry forums to expand visibility and strengthen external partnerships. Regulatory Compliance Ensure all safety and pharmacovigilance activities meet global regulatory requirements and internal standards. [...]
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[...] Collaborate with Regulatory Affairs on safetyrelated submissions, PSURs, and labelling updates for marketed and latestage products. Stay current with emerging global regulations and scientific advancements relevant to oncology safety. Provide strategic direction on regulatory interactions and inspection readiness related to safety and benefitrisk management. Deliver expert benefitrisk assessments to support filings, lifecycle management, and [. .. ] due diligence on new oncology assets, reviewing safety profiles and regulatory considerations. Identify risks and opportunities associated with external assets and partnerships. Requirements Education and Qualifications Qualified MD or equivalent medical degree (e. g. , MBBS, MBCh B, MBBCh, BMBS, BMBCh) . Professional Experience Extensive experience in postapproval drug safety and pharmacovigilance within the biopharmaceutical industry, including leadership of global teams and safety strategies. Experience across both small molecules and biologics. Strong background in oncology (preferred) or another specialised therapeutic area. Demonstrated [. .. ] and scientific excellence. Other Skills/ Attributes Passion for advancing oncology therapies and improving patient outcomes. Strong peopleleadership and teamdevelopment capabilities. Strategic thinking and analytical problemsolving. Expertise in regulatory compliance. Effective communicator and collaborative partner across functions. Seniority level Executive Employment type Fulltime Job function Science, Quality Assurance, and Strategy/ Planning Industries Biotechnology Research and Pharmaceutical Manufacturing #J-18808-Ljbffr 71178571 [. .. ]
Job gestern bei Jobleads gefunden
A global
medical device company is seeking a Clinical
Affairs Program Manager Europe. This role involves managing clinical trials in compliance with regulations, requiring a strong background in life sciences [...]
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[...] and clinical management. The candidate must be an effective communicator and collaborator with a track record of success in clinical trial execution, while also being willing to travel. This position offers a remote option and significant responsibilities that can influence patient care and product development. #J-18808-Ljbffr 71602017 [. .. ]
Job gestern bei Jobleads gefunden
• München, Bayern
[. .. ] of collaboration and excellence. Drive the EU4+UK P L, ensuring alignment with financial and strategic objectives. Develop and implement short and midterm plans to achieve sustainable profit [...]
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[...] growth. Collaborate with Medical Affairs, Market Access, and other crossfunctional teams to meet operational and performance goals. Establish and maintain effective product distribution models across EU4+UK and other European markets. Build longterm strategic partnerships with key stakeholders, including physicians, payers, and patient organizations. Represent Regeneron in global and regional forums, advocating for our corporate brand [. .. ] disease treatments. You excel in strategic thinking and datadriven decisionmaking. You thrive in dynamic, highgrowth environments and can manage complexity and ambiguity with a solutionoriented mindset. You are a skilled communicator who can navigate multicultural environments with ease. You value collaboration and have a proven ability to lead crossfunctional teams effectively. You are motivated by results and have a track record of achieving ambitious goals. You demonstrate integrity, transparency, and a commitment to building an inclusive and engaging team culture. To [. .. ]
Job gestern bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
Associate Director,
Medical Strategic Planning Operations The Associate Director, Medical Excellence/ Medical Operations plays a key leadership role in ensuring efficient, compliant, and scalable Medical
Affairs execution across the International [...]
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[...] Region. The role focuses on improving ways of working, optimizing review and approval processes, strengthening medical compliance and governance, and supporting country teams with guidance, tools, and best practices adapted to diverse local market needs. This role partners closely with Global Medical Affairs, Country Medical Directors, [. .. ] excellence projects. Familiarity with digital medical systems (e. g. , Veeva CRM) , medical dashboards, or analytics tools. Key Capabilities Structured thinker with strong organizational and project management skills. Excellent communicator able to simplify complexity and provide clear guidance. Collaborative mindset with ability to influence without authority. Practical, solutionoriented approach; comfortable working in evolving, fastpaced settings. Travel 1020 international travel expected. About Alnylam Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] of collaboration and excellence. Drive the EU4+UK P L, ensuring alignment with financial and strategic objectives. Develop and implement short and midterm plans to achieve sustainable profit [...]
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[...] growth. Collaborate with Medical Affairs, Market Access, and other crossfunctional teams to meet operational and performance goals. Establish and maintain effective product distribution models across EU4+UK and other European markets. Build longterm strategic partnerships with key stakeholders, including physicians, payers, and patient organizations. Represent Regeneron in global and regional forums, advocating for our corporate brand [. .. ] disease treatments. You excel in strategic thinking and datadriven decisionmaking. You thrive in dynamic, highgrowth environments and can manage complexity and ambiguity with a solutionoriented mindset. You are a skilled communicator who can navigate multicultural environments with ease. You value collaboration and have a proven ability to lead crossfunctional teams effectively. You are motivated by results and have a track record of achieving ambitious goals. You demonstrate integrity, transparency, and a commitment to building an inclusive and engaging team culture. To [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
[. .. ] good fit for this role and live in Brisbane, wed love you to apply. Responsibilities Manage life, disability, and income protection claims with a proactive approach. Assess [...]
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[...] claims by reviewing medical, contractual, and occupational details. Conduct phone interviews to understand members needs and plan their return to work. Communicate clearly with members, employers, and health professionals. Help improve processes and contribute to a positive team environment. About the role Were all about helping our members make the most of their money. [. .. ] you. About you Youre a people person who loves solving problems and making things better. You know how to handle sensitive situations with empathy and professionalism. Youre organised, a great communicator, and you thrive in a team setting. If you want to use your skills to help others and grow with us, wed love to hear from you. You have experience in customer service and handling client interactions. You have strong analytical and problem-solving skills. You have excellent verbal and [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Beratungs-/ Consultingtätigkeiten
[. .. ] the market Requirements Bachelors degree and excellent academic record 6+ years of consulting experience in an established strategic/ management consulting organization Experience in Life Sciences, particularly in [...]
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[...] the Commercial and Medical area Good understanding of Commercial, with proven expertise in two or more of the following areas: multi-channel strategy and optimization, product launch, go-to-market strategy, commercial model design, key account planning and management, segmentation and targeting, insight and analytics, brand strategy, and medical affairs Good understanding of commercial/ marketing technology and, ideally, Veevas platforms and solutions and how business consulting offerings can both leverage and support these Good understanding of the business capabilities and drivers underpinning digital technology in Health and life sciences and the market forces and trends driving industry changes in Health [. .. ] with people at all levels in an organization and quickly establish credibility Have a strong personal impact and are able to influence and persuade a range of stakeholders An effective communicator, verbally and written, in English and the local office language Nice to Have Graduate level qualification, Ph D, and/or MBA Strong network in the Top 20 Life Science companies Experience with digital technologies channels, analytics tools, emerging technology Experience working with Saa S solutions Understanding/ experience of AI and its applications [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
• Darmstadt, Hessen
Führungs-/ Leitungspositionen
[. .. ] data, and competitive landscape to shape compelling and credible brand narratives. Provide strategic input and leadership within the Global Brand Team and broader crossfunctional governance. Collaborate effectively [...]
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[...] with crossfunctional partners (Medical Affairs, Market Access, HEOR, Commercial Operations, Regulatory, and others) to ensure aligned and compliant execution. Identify strategic opportunities proactively, design initiatives to address them, and ensure excellence in implementation. Manage agencies, vendors, and project budgets to deliver highquality, timely outputs. Drive compliant execution of all marketing strategies, materials, and tactics. Represent [. .. ] is preferred Oncology and rare disease experience preferred Microsoft Office Brand planning Launch and tactical planning Strong track record of influencing key stakeholders and leadership with and without authority Clear communicator able to engage, influence and navigate crossfunctional stakeholders Team player and strong track record of collaboration Strong sense of urgency and ability to organize, prioritize, activate and execute Embody the Spring Works Values to act with empathy and humility to drive a culture that takes ownership and accountability for their [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
• Freiburg im Breisgau, Baden- Württemberg
[. .. ] and their patients. Together, lets advance the world of minimally invasive care. Job Description Primary Function of Position: The Contract Negotiator is key in Intuitives commercial contracting. [...]
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[...] As the main communicator for sales contracts, the Contract Negotiator works with Intuitives salesforce, leadership, internal management, over 10 departments, and customers for compliance and mitigation of risk in commercial contracts. The Contract Negotiator handles tasks like contract drafting, negotiating, and finalizing commercial contracts. This is done professionally in a high-pressure environment with [. .. ] sales agreements for Intuitives products and services. Act as a point of contact for digital, data, and privacy agreements, including Data Processing Agreements. Research. Stay updated on changes in the medical device industry affecting customer contracts. Provide recommendations and guidance based on industry best practices. Cross Functional Collaboration. Collaborate with internal stakeholders, like Business Development, Product Marketing, Legal, Regulatory Affairs, Service Department, Field Service, Manufacturing, and Executives. Understand business goals, incorporate Legals advice, and negotiate favorable terms. Prior to commercial launch of a new product, review and assess the impact of the new product on existing agreements or agreement templates. Coordinate drafting of or implement new agreement templates prepared or [. .. ]
Job am 06.11.2025 bei Jobleads gefunden
EU Regulatory Lead Director
Führungs-/ Leitungspositionen
[. .. ] our regulatory team, argenx is looking for an EU Regulatory Lead Director to support the rapid growth needed for successful commercialization. The role will report into the [...]
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[...] Head of Regulatory Affairs for Europe and New Territories, covering primarily the EU and requiring involvement in other territories (e. g. , UK, Switzerland, Israel, and the Middle East) . Responsibilities Provide strategic, operational and tactical regulatory insight on preapproval and postapproval activities. Help guide the organization on the appropriate filing strategy and coordinate [. .. ] requested. Provide regulatory leadership with postapproval activities. Monitor, interpret, and communicate changes to the global regulatory landscape. Serve as the regulatory affairs business partner to local commercialization teams. Partner with medical, legal, quality, PV, and distribution teams to ensure regulatory input is provided in a timely manner to support business decisions. Serve as the conduit between strategy within the assigned project team and the broader global regulatory and development teams. Skills and Competencies Affinity with science and ability to interact with [. .. ] industry trends, and health care business practices globally. Highly developed organizational skills and project management skills with demonstrated strengths in strategic planning, delegation, resource allocation, and workload prioritization. A clear communicator who can influence stakeholders effectively, both internally and externally, with outstanding presentation, written and verbal communication skills. You excel in a fastpaced, resultsdriven, highly accountable environment. You are pragmatic, yet creative and innovative and lead while rolling up your sleeves to get it done. You show strong leadership with proven [. .. ]
Job am 07.10.2025 bei Jobleads gefunden
Regulatory Affairs Manager
• Burgdorf, Bern
[. .. ] department, we are looking for a very experienced person on a high seniority level for our Diabetes Care Business in the B2C sector at our new Headquarter [...]
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[...] in Burgdorf. Regulatory Affairs Manager 80-100 Help us bring to market state-of-the-art medical technology solutions by optimizing processes and ensuring quality through your structured approach. Focus of this position is supporting our rapidly developing Diabetes Care (active and connected devices) Manage the development and implementation of RA strategies Support and prepare product submission documents with main focus on US Partner with business stakeholders [. .. ] experience in Regulatory Affairs with focus on medical devices Expertise in Active Medical Devices related regulations and guidance documents in US Excellent organizational and people skills Strong team player Strong communicator at a high stakeholder level Very good English knowledge (Level C2 or MT) Benefits Pension fund: Ypsomed covers 55 of the pension contributions Free sport facilities: Affordable or free gyms all over Switzerland Family-friendly: Financial contributions to childcare Working hours: Shiftwork, annual working hours, part-time Flex Work: Work [. .. ]
Job am 06.07.2025 bei Jobleads gefunden
Quality Assurance Manager
• Baden- Württemberg
Get AI-powered advice on this job and more exclusive features. Direct message the job poster from Barrington James Recruitment Consultant Quality Assurance UK Europe Job Summary: An innovative
medical [...]
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[...] device manufacturer, part of a dynamic global medtech group, is on the lookout for a driven quality expert to lead QA and RA activities at their site in Weil am Rhein, nestled in the vibrant south of Germany. This is your chance to shape compliance across the entire product lifecycle [. .. ] in coordination with headquarters Collaborate with the corporate quality team to harmonize quality approaches across all sites What Were Looking For: A degree in Life Sciences, Medical Technology, Quality, Regulatory Affairs, or a similar field (or an equivalent professional background) Solid experience in medical devices or other regulated industries (ideally 2+ years) Strong grasp of ISO 13485, MDR, 21 CFR 820, and general quality system frameworks Hands-on experience with tools like Track Wise, SAP, Share Point, or other QMS/ ERP systems Fluency in German and English, both written and spoken A confident communicator with excellent documentation skills and an analytical mindset Why Apply? Be part of a young, energetic team at a growing international medical technology company Take ownership in a pivotal role with high visibility and direct impact on quality and regulatory projects Enjoy a modern, flexible work environment with hybrid options [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
GYNEMED GmbH Co. KG
Regulatory Affairs Specialist (m/f/d) - Medical Devices (Full-time)
• Neustadt
We are seeking an experienced and proactive Regulatory
Affairs Specialist to join our international team and strengthen our global regulatory and quality management activities. In this role, you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] be responsible for driving regulatory strategies and submissions not only in Europe (MDR) and the U. S. (FDA) , but also across diverse international markets. By ensuring compliance with global [. .. ] fertility care by ensuring our products meet highest quality standards and global regulatory requirements. The position is based at our German subsidiary near Lübeck. Regulatory Affairs Specialist (m/f/d) Medical Devices (Full-time) Your tasks Lead and support cross-functional projects in regulatory affairs and quality management. Identify, interpret, and implement regulatory requirements across global markets, with a strong focus on international registrations outside the U. S. and EU. Independently prepare submissions and change notifications for competent authorities and international [. .. ] across diverse geographies. Independent, structured, and detail-oriented way of working combined with a collaborative mindset. Fluency in German and English; additional languages are an advantage for international registrations. Confident communicator with the ability to build strong internal and external relationships. Proficiency in MS Office applications. We offer An exciting and varied role in a collaborative, international environment. Direct involvement in global registration strategies, with significant responsibility for markets outside the EU and U. S. Flat hierarchies and the opportunity to [. .. ]
Job vor 4 Tagen bei Neuvoo.com gefunden
Meet Life Sciences
Global Head of Drug and Patient Safety
• Munich Muenchen
Führungs-/ Leitungspositionen
[. .. ] scientific, regulatory, and industry forums to expand visibility and strengthen external partnerships. Regulatory Compliance Ensure all safety and pharmacovigilance activities meet global regulatory requirements and internal standards. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Collaborate with Regulatory Affairs on safety-related submissions, PSURs, and labelling updates for marketed and late-stage products. Stay current with emerging global regulations and scientific advancements relevant to oncology safety. Provide strategic direction on regulatory interactions and inspection readiness related to safety and benefit-risk management. Risk Management Decision-Making Deliver expert benefit-[. .. ] due diligence on new oncology assets, reviewing safety profiles and regulatory considerations. Identify risks and opportunities associated with external assets and partnerships. Requirements Education and Qualifications Qualified MD or equivalent medical degree (e. g. , MBBS, MBCh B, MBBCh, BMBS, BMBCh) . Professional Experience Extensive experience in post-approval drug safety and pharmacovigilance within the biopharmaceutical industry, including leadership of global teams and safety strategies. Experience across both small molecules and biologics. Strong background in oncology (preferred) or another specialised therapeutic area. [. .. ] Other Skills/ Attributes Passion for advancing oncology therapies and improving patient outcomes. Strong people-leadership and team-development capabilities. Strategic thinking and analytical problem-solving. Expertise in regulatory compliance. Effective communicator and collaborative partner across functions. 70970010 [. .. ]
Job vor 4 Tagen bei Neuvoo.com gefunden
Jobijoba
Regulatory Affairs Specialist (m/f/d) - Medical Devices (Full-time)
• Schashagen
We are seeking an experienced and proactive Regulatory
Affairs Specialist to join our international team and strengthen our global regulatory and quality management activities. In this role, you will [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] be responsible for driving regulatory strategies and submissions not only in Europe (MDR) and the U. S. (FDA) , but also across diverse international markets. By ensuring compliance with global [. .. ] fertility care by ensuring our products meet highest quality standards and global regulatory requirements. The position is based at our German subsidiary near Lübeck. Regulatory Affairs Specialist (m/f/d) Medical Devices (Full-time) Your tasks Lead and support cross-functional projects in regulatory affairs and quality management. Identify, interpret, and implement regulatory requirements across global markets, with a strong focus on international registrations outside the U. S. and EU. Independently prepare submissions and change notifications for competent authorities and international [. .. ] across diverse geographies. Independent, structured, and detail-oriented way of working combined with a collaborative mindset. Fluency in German and English; additional languages are an advantage for international registrations. Confident communicator with the ability to build strong internal and external relationships. Proficiency in MS Office applications. We offer An exciting and varied role in a collaborative, international environment. Direct involvement in global registration strategies, with significant responsibility for markets outside the EU and U. S. Flat hierarchies and the opportunity to [. .. ]
Job am 25.10.2025 bei Neuvoo.com gefunden
Alimera
Medical Science Liaison
• Stuttgart
The
Medical Science Liaison facilitates and develops the relationship with the medical/ scientific community, particularly with Key Opinion Leaders (KOLs) but including other physicians and medical centres in Germany, [...]
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[...] by communicating scientific and medical product-related information to investigators and institutions. Works with all internal stakeholders to align business objectives. This is [. .. ] in South-West Germany who can communicate fluently in German, or at a minimum possess language proficiency at B2 or C1 level. RESPONSIBILITIES Serve as the primary field-based medical affairs representative on the ground to support medical affairs initiatives. Serve as the first point of contact for medical affairs onsite to support activities in the field of medical affairs. Provide appropriate project-based scientific training for KOLs. Identify and build relationships with national, regional and local KOLs. Identify KOLs for [. .. ] settings. Demonstration of proficiency in key skills and competencies. Proficiency in German at native speaker level and fluent in English, both written and spoken. SKILLS AND COMPETENCIES Effective and influential communicator-Highly articulate and persuasive during formal and informal presentations; able to convey complex, scientific information and data fluently to any audience, both in a one-to-one and in a team environment. Actively listens to others and is adept at confidently stating expert opinion while respecting the positions of others [. .. ]
Job am 16.10.2025 bei Neuvoo.com gefunden
Alimera
Medical Science Liaison
The
Medical Science Liaison facilitates and develops the relationship with the medical/ scientific community, particularly with Key Opinion Leaders (KOLs) but including other physicians and medical centres in Germany, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] by communicating scientific and medical product-related information to investigators and institutions. Works with all internal stakeholders to align business objectives. This is [. .. ] in South-West Germany who can communicate fluently in German, or at a minimum possess language proficiency at B2 or C1 level. RESPONSIBILITIES Serve as the primary field-based medical affairs representative on the ground to support medical affairs initiatives. Serve as the first point of contact for medical affairs onsite to support activities in the field of medical affairs. Provide appropriate project-based scientific training for KOLs. Identify and build relationships with national, regional and local KOLs. Identify KOLs for [. .. ] settings. Demonstration of proficiency in key skills and competencies. Proficiency in German at native speaker level and fluent in English, both written and spoken. SKILLS AND COMPETENCIES Effective and influential communicator-Highly articulate and persuasive during formal and informal presentations; able to convey complex, scientific information and data fluently to any audience, both in a one-to-one and in a team environment. Actively listens to others and is adept at confidently stating expert opinion while respecting the positions of others [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Medical Affairs Communicator pro Jahr?
Als Medical Affairs Communicator verdient man zwischen EUR 55.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Medical Affairs Communicator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 18 offene Stellenanzeigen für Medical Affairs Communicator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Medical Affairs Communicator Jobs?
Aktuell suchen 5 Unternehmen nach Bewerbern für Medical Affairs Communicator Jobs.
Welche Unternehmen suchen nach Bewerbern für Medical Affairs Communicator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Affairs Communicator Stellenangebote:
- GYNEMED GmbH Co. KG (2 Jobs)
- Alimera (2 Jobs)
- Meet Life Sciences (1 Job)
- Jobijoba (1 Job)
In welchen Bundesländern werden die meisten Medical Affairs Communicator Jobs angeboten?
Die meisten Stellenanzeigen für Medical Affairs Communicator Jobs werden derzeit in Bayern (4 Jobs), Baden-Württemberg (3 Jobs) und Niedersachsen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Medical Affairs Communicator Jobs?
Medical Affairs Communicator Jobs gehören zum Berufsfeld Redakteure & Journalisten.
