388 Jobs für Pharmaceutical Regulatory Manager
Stellenangebote Pharmaceutical Regulatory Manager Jobs
Job vor 2 Tagen bei StepStone gefunden
Tentamus Pharma Med Deutschland GmbH
• bundesweit, Bad Kissingen, Wien
Homeoffice möglich
Work-Life-Balance
[. .. ] our Headquarters in Berlin, Tentamus is represented in 100 locations across 23 countries, with just under 4, 000 highly trained staff members. Summary/ Objective We are seeking [...]
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[...] an experienced Sales Manager (m/f/d) CRO Services (DACH) to drive and manage strategic customer relationships across the DACH region. Reports to: Director Commercial Pharma DACH Supervisory Responsibilities: No Department: Commercial Pharma DACH Location: remote FLSA Classification: Full-Time This is a remote position, but the employee must reside in the DACH region, with Germany preferred. This role is pivotal in supporting the companys commercial growth by ensuring strong customer satisfaction, retention, and revenue expansion in the pharmaceutical and biotechnology sectors. The successful candidate will be responsible for managing key accounts, developing account strategies, and coordinating cross-functional teams to deliver GLP/ GMP/ GCP laboratory services that meet client expectations. While primarily remote, the role includes occasional customer visits and on-site meetings at Tentamus locations when clients [. .. ] CRO, pharmaceutical, or biotechnology industries Proven track record of achieving revenue targets in B2B environments Demonstrated experience in European market development and international business expansion Experience with GLP/ GMP/ GCP regulatory environments and laboratory services Experience in budget oversight Core Competencies Strategic thinker with the ability to translate vision into actionable plans and contribute to enterprise-level decision-making Advanced negotiation and relationship management skills Strong analytical skills, including pricing optimization and market analysis Proficiency in CRM systems, sales analytics tools, [. .. ]
Job vor 3 Tagen bei StepStone gefunden
Novanta
Medical Affairs Manager Medical Devices (m/f/d)
• Berlin
[. .. ] Insufflators, pumps and disposable tube sets, along with medical visualization and operating room integration technologies are the preferred solution for minimally invasive surgery applications. Summary The Medical [...]
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[...] Affairs (Clinical Affairs) Manager is held responsible for keeping a product or product group compliant with regulations and guidelines. The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/ MEDDEV. Primary Responsibilities Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR) , Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report) , and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products) [. .. ] ISO 14155) is required Knowledge of Clinical indication and application in Minimally Invasive Surgery is a plus Expert knowledge and experience in Medical Device/ Clinical investigation (ISO 14115) and/or pharmaceutical industries is a plus Fluent written and spoken English (at least C1) is required; German language skills is a plus Open and competent attitude when working with your stakeholders IT affinity and proficiency with the MS Office package Familiarity with AI tools is a plus Travel Requirements Travel by public [. .. ]
Job vor 14 Tagen bei StepStone gefunden
Dr. Falk Pharma GmbH
• Freiburg
Homeoffice möglich
[. .. ] well-being. We firmly believe that medical progress can only be achieved by working together. That is why we are looking for: Your tasks As the Quality Assurance [...]
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[...] (QA) GVP Manager within the GCP and GVP Quality Department, you will play a pivotal role in maintaining and enhancing the quality management framework in alignment with Good Pharmacovigilance Practice (GVP) guidelines. By collaborating with internal teams and external partners, you will ensure regulatory compliance and foster a robust culture of vigilance and safety. Your primary responsibilities will include, but are not limited to: Audits and Inspections: Plan, Conduct, and Follow Up on Pharmacovigilance Audits including oversight and training of external service providers and consultants (for audits) , ensuring adherence to company standards and [. .. ] reports and CAPA plansis accurate, up-to-date, and readily accessible Your qualification A minimum of 4-5 years of experience in pharmacovigilance quality assurance or related fields within the pharmaceutical industry, a Health Authority or a Contract Research Organisation (CRO) Proven experience in managing pharmacovigilance audit programs and teams, including conducting and overseeing global pharmacovigilance audits. Experience with regulatory inspections is preferred Degree in Life Sciences, Pharmacy or a related field In-depth understanding of global pharmacovigilance regulations and guidelines, [. .. ]
Job vor 2 Tagen bei JobMESH gefunden
PAUL HARTMANN AG
Regulatory Affairs/ Quality Assurance Manager-Support Development Marketing (f/m/d)
• Baden- Wurttemberg
[. .. ] (Qm/RA) (f/m/d) DEU-Heidenheim As Expert Component Qualification (Qm/RA) (f/m/d) for Procedure Packs, you will play a crucial role in ensuring our products meet
regulatory and quality standards [...]
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[...] across global markets. You will serve as a key interface between development, marketing and suppliers. If you have a passion for Regulatory and Quality in the medical device field, this role offers you the opportunity to make a tangible impact on patient safety and innovation. Responsibilities: Manage [. .. ] a technical qualification with relevant professional experience Formal training or hands-on experience in Regulatory Affairs is beneficial Solid understanding of Quality and Regulatory Affairs in the medical device or pharmaceutical industry Strong intercultural communication skills Analytical mindset with excellent problem-solving capabilities Proficient in both English and German (written and spoken) Benefits: Flexible working conditions, such as flexible working hours and mobile working International Mobile Working Attractive ways of combining work and family life, e. g. childcare subsidy 30 days [. .. ]
Job vor 7 Tagen bei JobMESH gefunden
medac Gesellschaft für klinische Spezialpräparate mbH
• Schleswig- Holstein
Work-Life-Balance
Global Market Access and HEOR
Manager (all genders) Wedelnear Hamburg About medac We are a strong community: with more than 2, 000 employees worldwide, we are committed to improving human [...]
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[...] health. Our work is more than just a job. With a career at medac, you can make a real difference in the industry. Look into this [. .. ] Provide market access insights and service for the in-licensing of new drugs, ensuring they meet market access and reimbursement requirements Collaborate cross-functionallywith regional market access teams, medical affairs, regulatory, and commercial functions to align global strategies with local requirements Your profile Academic degree in health economics, economics or natural sciences Several years of professional experience in a market access consultancy or market access role in the pharmaceutical industry Expertise and a proven track record in managing, creating, submitting, and defending dossiers projects, and health economic evidence before HTA agencies with a focus on AMNOG; additional background in other European markets is a plus Thorough understanding of health economic models and evidence Excellent project management skills and intercultural [. .. ]
Neu Job vor 7 Std. bei Mindmatch.ai gefunden
CTC Resourcing Solutions
Technical Project Manager (6896)
• AT- 2 Lavamünd
Homeoffice möglich
Pharma Technical Project
Manager 6896 Our client is a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation disorders, [...]
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[...] immunological diseases, enzyme deficiency diseases and other rare diseases. We are looking for a Pharma Technical Project Manager for a contract until Dec 2026 [. .. ] teams. The role ensures that all project deliverables are developed, reviewed, approved and executed in accordance with schedule requirements and within the approved budget and the applicable quality standards and regulatory expectations. The ideal candidate acts as the primary contact point for all involved stakeholders and external partners, which is key for a successful and compliant execution of CAPEX projects in GMP-regulated and capacity constraint environments. This person is also fluent in both German and English to effectively communicate with [. .. ] Swiss/ EU-Citizenship required Bachelors or Masters degree in Engineering (Mechanical, Electrical, Process, Chemical, or equivalent) . Minimum 5 years of experience in technical project execution within GMP-regulated environments (pharmaceutical, biotech, or life sciences) . Fluent in English German language skills are necessary (both languages in reading, writing and speaking) Solid understanding of c GMP, EU Annex 1, and engineering documentation. Proven experience in FMEA, technical troubleshooting, and interfacing with multiple departments. Strong communication and organizational skills, with the ability to [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Tandem Diabetes Care
• AT- 3 St. Pölten
[. .. ] through direct patient care that support diabetes education in relation to insulin pump therapy and other advanced diabetes management skills to gain prospective and retain existing customers. [...]
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[...] Interact with Clinical Manager for guidance on technical and training issues. Collaborate with appropriate internal teammembers to identify and address postsale product issues, and additional patient education training needs. Provide products/ services information directly to the consumer/ end user via health fairs, conventions or in conjunction with promotions. Attend and participate in all corporate [. .. ] software (CRM) , for all business dealings within assigned territory. Collaborate with Sales, Medical Affairs, and Customer Support teams to deliver a seamless customer experience. Uphold company compliance with all regulatory, privacy, and legal requirements. YOURE AWESOME AT Excellent communicator, able to earn trust with both HCPs and patients. Proficient in Type 1 and Type 2 diabetes selfmanagement, including: insulin pumps, AID systems, CGMs, infusion sets, carbohydrate counting, and emergency protocols. Proven ability to work independently and drive strategically results in [. .. ] company policy. Able to travel to the U. S. or Switzerland for training and internal meetings as required. Fluent in German and English language. EXTRA AWESOME Medical device consultant or pharmaceutical sales representative Nursing background or Dietitian or equivalent combination of education and applicable job experience. Diabetes Care experience is an absolute plus. Continuing education on patient education on the technical use of diabetes technology and special considerations related to pump therapy in the marketplace. Minimum 2 years of experience in [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
CTC Resourcing Solutions
CAPEX Project Manager Pharma (6896)
• AT- 2 Lavamünd
CAPEX Project
Manager Pharma 6896 Our client is a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation [...]
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[...] disorders, immunological diseases, enzyme deficiency diseases and other rare diseases. We are looking for a CAPEX Project Manager for 12 months contract, with potential [. .. ] teams. The role ensures that all project deliverables are developed, reviewed, approved and executed in accordance with schedule requirements and within the approved budget and the applicable quality standards and regulatory expectations. The ideal candidate acts as the primary contact point for all involved stakeholders and external partners, which is key for a successful and compliant execution of CAPEX projects in GMP-regulated and capacity constraint environments. This person is also fluent in both German and English to effectively communicate with [. .. ] or B. Sc. or higher or equivalent. 5+ years of successful project management and leadership experience on mid-sized Cap Ex projects with high complexity in the chemical, biotech-or pharmaceutical industry. Proven project management skills including contract management and controlling. Proven experience and knowledge in chemical, biotech or pharmaceutical process and infra engineering. Proven experience in c Gx P and qualification. Languages: German and English fluent in written and spoken J-18808-Ljbffr 83948862 [. .. ]
Job vor 2 Tagen bei Mindmatch.ai gefunden
Grünenthal Group
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] and discover the difference you can make. What The Job Looks Like Set the strategic direction to build the statistical and clinical unbiased evidence for all clinical [...]
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[...] phases (IIII) , regulatory submissions, market access and life cycle management. Contribute in collaboration with all scientists in DEV to design the trials for Phase IIII (Po C, late development and life cycle management) , including the definition of Go/ No Go criteria ensuring best possible decision Oversee and support creation of the statistical analysis [. .. ] working model What Youll Bring To The Table Ph D in biostatistics, statistics, mathematics or MSc from highranked university, data scientist or equivalent At least 10 years of experience in the pharmaceutical industry Hands on experience in programming the analyses of data and data mining in SAS and R and other software Profound knowledge of most advanced statistics, probability and mathematics Experience in designing, reviewing and providing input into SOW for external service providers in collaboration with other functions Be able to [. .. ] writing, additional language skills beneficial Become part of our multicultural and interdisciplinary team and join us on an exciting journey towards a World Free of Pain Heiko Hagedorn, the Hiring Manager J-18808-Ljbffr 83949496 [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Suma Medtec
Senior Regulatory Affairs Lead, Medical Devices
• AT- 9 Wien
Work-Life-Balance
A medical technology company in Austria is seeking a
Regulatory Affairs
Manager to lead the regulatory lifecycle of medical devices. The role requires a minimum of 5 years [...]
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[...] of experience in regulatory affairs within the medical device or pharmaceutical industry, and proficiency in English. Responsibilities include formulating global regulatory strategies, collaborating with cross-functional teams, and authoring necessary documentation. The position offers a competitive salary, remote work options, and a strong emphasis on work-life balance. J-18808-Ljbffr 83451985 [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Rhythm Pharmaceuticals Inc.
• AT- 9 Wien
[. .. ] GSA team, you will focus on advancing medical and scientific initiatives in Rare MC4R pathway diseases. In close collaboration with the national and international Medical Affairs teams, [...]
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[...] the Scientific Affairs Manager (SAM) will provide scientific leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Austria. Responsibilities and Duties Serve as the Scientific Affairs Manager for Austria and as a member of the international Medical Affairs team. Contribute [. .. ] projects, including identification and training of sites and assistance with patient recruitment. Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements. Collaborate closely with Commercial, Regulatory, Pharmacovigilance and Market Access. Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations. Participate in local medical and cross-functional projects and initiatives. Ensure effective and compliant communication with internal and external stakeholders. Support the commercial team and HCPs with knowledge [. .. ] multidisciplinary care including patient support programs. Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways. Qualifications and Skills Advanced degree in pharmaceutical, scientific, or medical field (Pharm D, Ph D, MD) . At least 6 years of experience in a comparable role within the biopharmaceutical sector, ideally with a focus on rare diseases. Excellent communication skills and scientific expertise, especially in presenting to diverse audiences. Proven skills and ability to work in a cross [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Suma Medtec
Regulatory Affairs Manager-Medical Devices
• AT- 9 Wien
Position:
Regulatory Affairs
Manager Medical Devices Level: Mid-Level or Senior Type: Internal, Full-time Location: Kufstein or Vienna, Austria (work permit provided for non EU employees, must be willing [...]
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[...] to relocate) Job description This is a fulltime role for a Regulatory Affairs Manager based in Austria. The position will offer the opportunity to work [. .. ] Office) , and present online in video conferences. Candidate profile and required qualifications Relevant Experience: a minimum of 5 years in a Regulatory Affairs role within the medical device or pharmaceutical industry is required (e. g. , developing medical devices, Sa MD, combination products, IVDs) . Studies: BS, MS, or Ph D. in a field applicable to life science or international policy. Experience working with crossfunctional teams in medical device development from concept to market launch. Direct experience authoring regulatory documentation for US [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
AOP Health
• AT- 9 Wien
Homeoffice möglich
[. .. ] therapies for rare diseases and in critical care. To enhance our team in Vienna we are looking for a: We are looking for an experienced and scientifically [...]
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[...] driven Medical Information Manager to deliver a highquality, compliant, and insightdriven Medical Information (MI) service globally. You will oversee the global medical information management system, ensuring data integrity, regulatory compliance, and operational excellence. What Your Day To Day Will Look Like Provide highquality, evidencebased responses to medical inquiries, ensuring compliance with regulatory and legal requirements. Conduct literature searches and analyze clinical data to support accurate scientific communication. Develop, review, and maintain Medical Information content (Standard Responses, FAQs) within Veeva. [. .. ] Affairs teams globally. Your Qualifications And Experience Advanced degree in Life Sciences, Pharmacy, or Medicine 5+ years of experience in Medical Information, Medical Affairs, or a related function within the pharmaceutical industry. Strong scientific background with excellent analytical and medical writing skills. Experience working with global teams and external vendors. Familiarity with Veeva Medical Information systems (e. g. , Med Inquiry) is an advantage. Solid understanding of regulatory, pharmacovigilance, and data privacy requirements. Strong communication, presentation, and stakeholder management skills. High [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Biogen
(Sr) Medical Manager, Rare Diseases (f/m/d) Switzerland/Austria
• AT- 9 Wien
Based out of our office in Vienna (hybrid working model) we are recruiting for a (Sr) Medical
Manager, Rare Diseases (f/m/d) CHAT (Switzerland/Austria) About This Role: The (Sr) Medical [...]
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[...] Manager, Rare Diseases CHAT (f/m/d) is a key medical and scientific expert for both internal and external stakeholders in various Therapeutic Areas, including Rare Diseases for Austria and Switerland. The incumbent will be responsible [. .. ] publications Be updated and accurate for medical reviews, share scientific expertise on data and all material related to assigned TAs to be used/shared/disseminated with external stakeholders, including commercial, regulatory affairs, market access, corporate affairs Closely collaborates with ICo E/ Global Medical to share best practices and experience from a local level and raise potential needs Provide medical input and support into Regulatory Affairs, Value and Access, and Marketing strategies Attend and share insights from national and international congresses Conduct/ attend/[. .. ] D. , D. Sc. , Master, Ph. D. , or M. D. ) or medical/ technical scientific training background combined with an experience of more than 5-7 years in pharmaceutical industry and/or in Medical affairs At least 5-7 years of experience in the pharmaceutical industry with a focus on specialty care, particularly in Neuroscience and/or in orphan diseases (e. g. , Medical Affairs, Clinical Research) Prior experience in Neurology is strongly preferred, experience in Immunology is a [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Astra Zeneca
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] long-term value. As a senior leader and member of the AZ Austria Senior Management Team, the role provides clear direction to the Market Access organization, navigating increasing [...]
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[...] system complexity, regulatory requirements, and stakeholder expectations with confidence and agility. It combines strategic foresight with operational excellence, representing the company in critical external negotiations while fulfilling key legal and regulatory responsibilities. Beyond market access delivery, the role plays a pivotal part in building Austria as a talent factorydeveloping highperforming, futureready teams, fostering [. .. ] compliance with the Code of Conduct and all relevant policies and standards. You provide strategic leadership and direction to the Market Access Team, including the Market Access Lead, Market Access Manager, Market Access Assistant, and Pricing Manager, with functional oversight of Legal Counsel. The role acts as the legal signatory in the capacity of Handelsrechtlicher Geschäftsführer and assumes the responsibilities of Deputy Verantwortliche Person in accordance with Arzneimittelbetriebsordnung (AMBO) regulations. Your leadership scope includes managing a diverse team, fostering strong strategic [. .. ] Access team and other functions. Skills/ Experience Medical, science and/or economic/ legal education (university degree) . Knowledge about Astra Zeneca product portfolio. Minimum 5 years jobrelated experiences in the pharmaceutical industry (Market Access) . Proven experience and track record of strong content and lateral leadership skills, eventually linemanagement. Ideally experiences in Pharmacoeconomics/ Health Economics and evidence based medicine. Fluency in written and spoken German English. Possesses commercial awareness, businessacumen and thinking, able to apply this without compromising scientific and ethical [. .. ]
Job vor 10 Tagen bei Mindmatch.ai gefunden
IQVIA LLC
Local Trial Manager-Sponsor Dedicated
• AT- 9 Wien
Local Trial
Manager-Sponsor Dedicated page is loaded # # Local Trial Manager-Sponsor Dedicatedlocations: Vienna, Austriatime type: Full timeposted on: Posted Todayjob requisition id: R1531480The IQVIA sponsor-dedicated Clinical Functional Service [...]
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[...] Partnerships (Clinical FSP) department is supporting our clients project team in the execution of clinical trials. Joining the team provides the [. .. ] based throughout Austria. Your responsibilities will include: Services rendered will adhere to applicable companys standard operating procedures (SOPs) , work instructions, policies, codes of Good Clinical Practice (GCP) , local regulatory requirements, etc. Prepare or contribute to high level budget estimate in response to Request for Services followed by detailed budget proposal. Ensure overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensure services are delivered per contract. Act as primary company contact for [. .. ] of functional area in process initiatives, as required and if applicable. Qualifications: Masters or higher-level degree in life science. Minimum of 5 years of clinical research experience in the pharmaceutical industry or CRO plus 1-3 years of local clinical trial management experience. Therapeutic area expertise in the field of Oncology is a must. Strong working knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
IQVIA
• AT- 9 Wien
[. .. ] to work with one single client and to manage clinical research projects in different therapeutic areas. We currently offer the exciting opportunity to join the FSP team [...]
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[...] as Local Trial Manager (m/w/d) in full-time and work home-based throughout Austria. Your Responsibilities Will Include Services rendered will adhere to applicable companys standard operating procedures (SOPs) , work instructions, policies, codes of Good Clinical Practice (GCP) , local regulatory requirements, etc. Prepare or contribute to high level budget estimate in response to Request for Services followed by detailed budget proposal. Ensure overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensure services are delivered per contract. Act as primary company contact for [. .. ] of functional area in process initiatives, as required and if applicable. Qualifications Masters or higher-level degree in life science. Minimum of 5 years of clinical research experience in the pharmaceutical industry or CRO plus 1-3 years of local clinical trial management experience. Therapeutic area expertise in the field of Oncology is a must. Strong working knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Grünenthal Group
Senior Medical Affairs Manager DACH (m/w/d)
• AT- 9 Wien
[. .. ] and review of Standard Response Documents, ensuring consistency, scientific rigor, and alignment with internal guidance. Acting as a delegate on behalf of the Informationsbeauftragter for DACH, ensuring [...]
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[...] compliance with regional regulatory and communication requirements. Serving as a strategic partner within brand teams, ensuring medical excellence in omnichannel engagement. Gathering and analyzing scientific insights from the field to inform medical and commercial strategies. Shaping the scientific content of congresses, symposia, advisory boards, webinars, and other medical education events. Supporting regulatory and pharmacovigilance [. .. ] successfully, you should bring: A successfully completed degree in Medicine, Pharmacy, or a natural science discipline, ideally complemented by a Ph D. At least 3 years of relevant experience in the pharmaceutical industry. A deep understanding of the pharmaceutical environment and solid knowledge of the DACH healthcare systems. Comprehensive knowledge of applicable legal and regulatory requirements, with the ability to apply them confidently in daily practice. A scientific mindset with strong analytical abilities and a structured, evidencebased approach to work. Proven ability to effectively manage external agencies and scientific content providers. Fluency in German and businesslevel English, both written and spoken. Jan Jastorff, the Hiring Manager J-18808-Ljbffr 82511742 [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Rhythm Pharmaceuticals
Scientific Affairs Manager, Austria
• AT- 9 Wien
[. .. ] GSA team, you will focus on advancing medical and scientific initiatives in Rare MC4R pathway diseases. In close collaboration with the national and international Medical Affairs teams, [...]
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[...] the Scientific Affairs Manager (SAM) will provide scientific leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in Austria. Responsibilities and Duties Serve as the Scientific Affairs Manager for Austria and as a member of the international Medical Affairs team. Contribute [. .. ] projects, including identification and training of sites and assistance with patient recruitment. Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements. Collaborate closely with Commercial, Regulatory, Pharmacovigilance and Market Access. Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations. Participate in local medical and cross-functional projects and initiatives. Ensure effective and compliant communication with internal and external stakeholders. Support the commercial team and HCPs with knowledge [. .. ] multidisciplinary care including patient support programs. Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways. Qualifications and Skills Advanced degree in pharmaceutical, scientific, or medical field (Pharm D, Ph D, MD) . At least 6 years of experience in a comparable role within the biopharmaceutical sector, ideally with a focus on rare diseases. Excellent communication skills and scientific expertise, especially in presenting to diverse audiences. Proven skills and ability to work in a cross [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
Talentor Austria
(Senior) Clinical Operations Project Manager
• AT- 9 Wien
Homeoffice möglich
Become part of the R D team and be responsible for an innovative product pipeline in the area of Clinical Operations Our client, Orpha Trade, is a small and agile [...]
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[...] pharmaceutical company headquartered in the heart of Vienna. The company specializes in the development and commercialization of innovative medicinal products and is currently experiencing a dynamic growth phase. With efficient structures, short decisionmaking paths, and a high degree of autonomy, Orpha Trade is preparing to launch a Phase I study for [. .. ] the clinical development program. To strengthen the R D team, we are seeking an experienced, handson professional who assumes operational responsibility while also contributing strategic input. (Senior) Clinical Operations Project Manager (w/m/x) YOUR FUTURE ROLE Build the Clinical Operations structure and further develop existing SOPs and processes Establish and execute clinical development activities for an innovative biologic, including identification of process gaps and ensuring sponsor readiness for the first Phase I study Develop and implement GCP-compliant clinical trial [. .. ] Pharmacy, Biotechnology) or equivalent professional experience At least 5 years of experience in Clinical Operations/ Project Management on the sponsor or sponsorrepresentative side Solid knowledge of clinical drug development and regulatory requirements (ICHGCP, EUCTR, FDA regulations) Proven expertise in vendor and CRO management as well as e TMF systems and clinical data processes Strong project management skills, including budgeting, resource planning, and stakeholder management High degree of autonomy, handson mentality, and enthusiasm for building new structures Pragmatic, resilient, and adaptable personality with [. .. ]
Job am 25.02.2026 bei Mindmatch.ai gefunden
Talentor Austria
Clinical Operations Architect Phase I Biologic
• AT- 9 Wien
A growing
pharmaceutical company in Vienna is seeking an experienced (Senior) Clinical Operations Project
Manager to build their Clinical Operations from the ground up. The ideal candidate will [...]
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[...] have at least 5 years of experience in Clinical Operations or Project Management and a thorough understanding of clinical drug development and regulatory requirements. This role offers flexible working hours and a significant opportunity to influence the clinical development program of an innovative biologic. J-18808-Ljbffr 81902941 [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
Exyte
Lead Engineer Mechanical Sanitary (m/f/d)
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] plant utility planning and the associated sanitary system, participate in 3D model and design reviews and are available as contact person Compliance with applicable international norms, standards, [...]
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[...] GMP regulations and regulatory requirements are part of your area of responsibility You also prepare the equipment and material lists as well as the performance directory Cost determination and price comparisons are also part of your tasks Show your expertise Completed studies in the field of mechanical engineering, process engineering or building technology and several years of professional experience in a comparable position, e. g. as a senior engineer, project manager for building services/ sanitary systems/ MEP and so on Extensive knowledge of Plant Utility and sanitary systems and project experience, ideally within the pharmaceutical industry Knowledge of technical requirements (norms, standards, VOB, etc. ) Expertise in MS Office, CAD and calculation software You are characterized by independent work as well as strong communication and argumentation skills Very good knowledge of German and English, both written and spoken Mobility (class B drivers license) and willingness [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
New Business
Brand Manager, Breakthrough Launch CVRM (m/w/d)
• AT- 9 Wien
Brand
Manager, Breakthrough Launch-CVRM Contract: Full-time About the role Join Astra Zeneca to lead brand management for a breakthrough launch product in Cardiovascular, Renal and Metabolism (CVRM) - the [...]
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[...] first innovation to this category in a decade. You own the annual brand budget for costs and sales, set bold targets, track performance rigorously, and craft a sharp, insight-led go-to-market (GTM) strategy. You know how to launch a pharmaceutical brand with excellence. Key responsibilities Strategic You lead the development of the GTM strategic plan aligned to the Global brand strategy. You make insight-led decisions, staying constantly informed about market conditions and translating them into differentiated marketing concepts. You define, track, and course-correct against clear brand KPIs. You [. .. ] brand trackers, sales analyses, and market monitoring. You share best practices across the region and collaborate through global brand forums with AZ global and operational teams. Operational You partner with Regulatory Affairs, Market Access, Medical, and Sales to deliver compliant, high-impact execution across promotional materials, educational events, patient support programs, and omnichannel campaigns. You work closely with the sales force, designing product-specific marketing training that powers field impact. You build strong relationships with opinion leaders and represent Astra Zeneca [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
Senior Clinical Evaluation Manager (m/f/d)
• AT- 9 Wien
[. .. ] history of my Sugr Roche. Heres what were looking for: We are seeking a dedicated and expert Medical Doctor with academic experience to join our team as [...]
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[...] a Senior Medical Solutions Manager/ Senior Clinical Evaluation Manager, focusing on our cutting-edge Diabetes Care and Diagnostics portfolio. You bring strong experince with clincial evaluations and can serve as a subject matter expert in the team. This critical role serves as the medical and clinical authority for our diabetes-related devices, including Medical Device [. .. ] of our life-changing technologies. Your upcoming mission: Data Generation Clinical Support: Author and lead the clinical evaluation efforts for Diabetes Care devices, including pumps and CGMs, ensuring alignment with regulatory requirements. Provide expert medical input for critical safety and regulatory documents, including Clinical Evaluation Reports, Medical Risk Assessments (MRA) , and Risk Enablers. Identify local data gaps and lead data generation activities; design and oversee Post-Market Clinical Follow-Up (PMCF) plans and studies. Serve as a Study Safety Officer [. .. ] evaluations are a plus An extended skill set and academic or industry experience in Diabetes and/or a related field is required. Proven experience in a relevant role within the pharmaceutical, medical device, or biotechnology industry (e. g. , Clinical Evaluator for medical devices) . Solid understanding of the Diabetes and its technical and medical state-of-the-art. Solid understanding of the CGM business and its technical and medical state-of-the-art. Demonstrated experience in developing and managing relationships [. .. ]
Job am 22.02.2026 bei Mindmatch.ai gefunden
allaboutvienna
Healthcare Medical
• AT- 9 Wien
[. .. ] the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted. . . Permanent Iqvia Austria-Wien 9 hours [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ago Project Manager, Study Operations, Cronos Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an. . . Permanent Austria-Wien 9 hours ago Public Affairs Manager (f/m/d) Job Description Summary #LI-Hybrid Location: Vienna, Austria At Novartis, one of Austrias leading pharmaceutical companies, we are driven by our purpose: to improve and extend peoples lives. We. . . Permanent Dedalus Austria-Wien 9 hours ago Fullstack Developer (m/f/d) Location: Vienna, Austria (Hybrid possible) About the Role Build toptier enterprise web applications for the healthcare industry and contribute to scalable, reliable. [. .. ] Austria on market and sales strategy issues along the entire life cycle of a product. This includes market and competition analyses, . . . Permanent Iqvia Austria-Wien 9 hours ago Regulatory Start Up Specialist I, IQVIA Med Tech, Austria Regulatory Start Up Specialist I, IQVIA Med Tech, Austria Join to apply for the Regulatory Start Up Specialist I, IQVIA Med Tech, Austria role at IQVIAJob Overview Perform tasks at a country level. . . Permanent Austria-Wien 9 hours ago Senior [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmaceutical Regulatory Manager pro Jahr?
Als Pharmaceutical Regulatory Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmaceutical Regulatory Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 388 offene Stellenanzeigen für Pharmaceutical Regulatory Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmaceutical Regulatory Manager Jobs?
Aktuell suchen 102 Unternehmen nach Bewerbern für Pharmaceutical Regulatory Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmaceutical Regulatory Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmaceutical Regulatory Manager Stellenangebote:
- Next Pharma (14 Jobs)
- Thermo Fisher Scientific (11 Jobs)
- CHEPLAPHARM Arzneimittel GmbH (9 Jobs)
- Essence Investment AG (8 Jobs)
- Dr. Falk Pharma GmbH (7 Jobs)
- ITL Germany (6 Jobs)
In welchen Bundesländern werden die meisten Pharmaceutical Regulatory Manager Jobs angeboten?
Die meisten Stellenanzeigen für Pharmaceutical Regulatory Manager Jobs werden derzeit in Bayern (50 Jobs), Berlin (33 Jobs) und Baden-Württemberg (30 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmaceutical Regulatory Manager Jobs?
Pharmaceutical Regulatory Manager Jobs gehören zum Berufsfeld Regulatory Affairs & Management.
