Medical Affairs Communicator Stellenangebote


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Job vor 13 Tagen bei Stellenanzeigen.de gefunden GYNEMED GmbH Co. KG

Regulatory Affairs Specialist (m/f/d) - Medical Devices (Full-time)

• Schleswig- Holstein 23730 Schashagen 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 11 Tagen bei JobMESH gefunden GYNEMED GmbH Co. KG Regulatory Affairs Specialist (m/f/d) - Medical Devices (Full-time) • Schleswig- Holstein 23730 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 be [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 11 Tagen bei Jobleads gefunden

Global Head of Drug and Patient Safety

• 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. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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. Risk Management Decision Making Deliver expert benefitrisk assessments to support [. .. ] 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. #J-18808-Ljbffr 71178571 [. .. ]

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Job gestern bei Jobleads gefunden

Head of Compliance Vienna, Austria-Wien

• Klosterneuburg, Niederösterreich Niederoesterreich Führungs-/ Leitungspositionen [. .. ] the Launch of New Markets as well as the Integration of Acquired Assets Represent the companys interests in International Institutions (e. g. FATF) as coordinated by the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] department International Regulatory Affairs As part of the Western Union Group, assess WUIBs compliance with groupwide compliance standards, as well as contribute to group-level assessments of the effectiveness of strategies, procedures, and controls across Group entities Organizing, and in some instances developing, occasional or regular provision of training for AML/ CFT and Sanctions [. .. ] in regulatory policies Effective leader for a diverse group of employee levels and job functions Able to manage a regionally diverse team Strong, decisive, bottom-line and actionoriented manager. Effective communicator on both an individual and group level, and both orally and written. Team player who works effectively with others to identify and resolve issues. Effectively motivates to achieve common goals. Shares information and keeps team members and supervisors informed. Strong strategic thinking and planning skills including Understanding of technology and [. .. ] benefits below and note that your Recruiter may share additional rolespecific benefits during your interview process or in an offer of employment. Your Austria specific benefits include : Comprehensive life medical cover Contributory pension plan Luncheon vouchers Other partner discounts Western Union values inperson collaboration, learning, and ideation whenever possible. We believe this creates value through common ways of working and supports the execution of enterprise objectives which will ultimately help us achieve our strategic goals. By connecting facetoface, we are [. .. ]

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Job gestern bei Jobleads gefunden Head of Compliance Vienna, Austria-Wien • Mödling, Niederösterreich Niederoesterreich Führungs-/ Leitungspositionen [. .. ] the Launch of New Markets as well as the Integration of Acquired Assets Represent the companys interests in International Institutions (e. g. FATF) as coordinated by the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] department International Regulatory Affairs As part of the Western Union Group, assess WUIBs compliance with groupwide compliance standards, as well as contribute to group-level assessments of the effectiveness of strategies, procedures, and controls across Group entities Organizing, and in some instances developing, occasional or regular provision of training for AML/ CFT and Sanctions [. .. ] in regulatory policies Effective leader for a diverse group of employee levels and job functions Able to manage a regionally diverse team Strong, decisive, bottom-line and actionoriented manager. Effective communicator on both an individual and group level, and both orally and written. Team player who works effectively with others to identify and resolve issues. Effectively motivates to achieve common goals. Shares information and keeps team members and supervisors informed. Strong strategic thinking and planning skills including Understanding of technology and [. .. ] benefits below and note that your Recruiter may share additional rolespecific benefits during your interview process or in an offer of employment. Your Austria specific benefits include : Comprehensive life medical cover Contributory pension plan Luncheon vouchers Other partner discounts Western Union values inperson collaboration, learning, and ideation whenever possible. We believe this creates value through common ways of working and supports the execution of enterprise objectives which will ultimately help us achieve our strategic goals. By connecting facetoface, we are [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden

Director Market Access Reimbursement

• Zug Führungs-/ Leitungspositionen [. .. ] pricing and market access activities including market access and pricing research for new products and pricing committees, including pricing for OOP (Out of Pocket) markets. Works closely [...]
MEHR INFOS ZUM STELLENANGEBOT[...] with International Marketing, Medical Affairs, Distributor Managers, and Country Managers to align on activities to support reimbursement initiatives. Consistent demonstration of exceptional leadership qualities, including but not limited to the ability to attract and retain the best team, foster a culture of high performance, lead with integrity, humility, accountability, and courage, and set a clear [. .. ] communicate effectively at all levels of the organization and with outside audiences, including reimbursement agencies. Excellent analytical skills and business acumen. Ability to work as part of a team; Strong communicator with ability to maintain open communication with internal employees, managers and customers as needed. Can do attitude. Committed to the patient mission and vision of Exact Sciences. Strive for excellence in all aspects of his/ her performance and is committed to continuous self-evaluation and development. #J-18808-Ljbffr [. .. ]

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Job vor 7 Tagen bei Jobleads gefunden

Commercial Director DACH

Führungs-/ Leitungspositionen [. .. ] high growth business. The 2026-30 strategy plan forecasts revenue growth from 42.4m to 85m by 2030 and with increased strategic focus, direct investment in sales, marketing, governmental [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and medical affairs and implementation of commercial excellence initiatives with our team and partners. The position is a key role for the business, and the incumbent should be considered to have potential to take on further commercial roles within the business including potential for succession to a more senior role in Commercial. Key [. .. ] in leveraging a Commercial Excellence system/platform to implement and drive territory key account management, training, performance tracking analysis and partner/ distributor management. You are a clear, effective and engaging communicator. This includes the ability to analyse, critique and synthesize ideas and adapt, and coach others to adapt, the nature, tone, length and detail of communication to the audience. You have a demonstrable track record of displaying good judgement when it comes to business decisions, people and performance as well as [. .. ]

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Job vor 10 Tagen bei Jobleads gefunden

Regional Manager Rare Disease Europe

• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 10 Tagen bei Jobleads gefunden

European Clinical Affairs Program Manager (Remote + Travel)

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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] life sciences 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 [. .. ]

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Job vor 14 Tagen bei Jobleads gefunden Regional Manager Rare Disease Europe • München, Bayern [. .. ] culture of collaboration and excellence. Drive the EU4+UK P L, ensuring alignment with financial and strategic objectives. Develop and implement shortand midterm plans to achieve sustainable profit [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job am 25.11.2025 bei Jobleads gefunden Senior Business Consultant-Commercial • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job am 17.11.2025 bei Jobleads gefunden Spring Works: Global Brand Director-GOMEKLI/ EZMEKLY (all genders) • 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job am 13.11.2025 bei Jobleads gefunden Contract Specialist (m/w/d) • 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. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 13 Tagen bei Neuvoo.com gefunden Meet Life Sciences Global Head of Drug and Patient Safety • Munich 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 [. .. ]

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Job vor 13 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 [. .. ]

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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.


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), Thüringen (3 Jobs) und Schleswig-Holstein (3 Jobs) angeboten.


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Dauer: 0.0378 s., Vers. V.2025-d-2008-Ind-141