70 Jobs für Internal Medicine Expert
Stellenangebote Internal Medicine Expert Jobs
Job vor 8 Tagen bei Mindmatch.ai gefunden
Contextflow
• AT- 9 Wien
Führungs-/ Leitungspositionen
[. .. ] according to MDR and ISO 13485. Act as Management Representative serve as the primary point of contact for quality-related topics within the executive team. Manage Audits coordinate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and lead internal and external audits, including communication with Notified Bodies. Maintain Operational Quality own the CAPA process, supplier management, employee training, software tool validation and other processes to ensure organizational excellence. Requirements What we are looking for: Quality Management Experience extensive experience in quality management and regulatory affairs within the medical device industry (Saa MD in Radiology AI preferred) . Regulatory Expertise expert knowledge of ISO 13485, MDR (EU) 2017/ 745, IEC 62304, ISO 14971, ISO 27001, FDA, and MDSAP. Strategic Thinking ability to define and track OKRs that align with the companys quality policy and mission. Handson Mindset comfortable defining longterm regulatory strategy while also executing the administrative tasks necessary to maintain [. .. ] team, characterized by close collaboration and sharing of knowledge across boundaries of individual fields. We are focused on developing cuttingedge deep learning techniques that serve the rapidlyadvancing needs of precision medicine and clinical practice. We place a huge emphasis on the wellbeing of all our team members. Become part of a team of AI medical image processing experts. Thrive in a young, dynamic learning environment where you can grow. Work on the exciting topic of certification of AI software technology. Work [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Mundipharma International
Associate Quality Manager (f/m/d)
• AT- 9 Wien
[. .. ] CEE markets to ensure operational compliance. Issue Resolution and support the management of regional quality issues, including complaints, product recalls, and returns. Audit Management-Lead the preparation and [...]
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[...] support for internal and external GDP/ GMP audits and regulatory inspections. QMS Development-Maintain and evolve the Quality Management System in accordance with EU GDP/ GMP guidelines and national legislation. Quality Controls-Manage deviations, CAPAs, change controls, and conduct thorough quality risk assessments. Oversee technical documentation Quality/ Technical Agreements, pharmaceutical licenses, and ensure [. .. ] to monthly reviews and Product Quality Reviews (PQRs) . Compliance Monitoring-Conduct self-inspections and manage NMVO alerts and related regional contracts. Act as a proactive interface for stakeholders, providing expert quality guidance and training compliance support to regional teams. What youll bring University degree in Pharmacy would be ideal but may be open to other Scientific Degrees in areas such as Chemistry, Biology, Human or Veterinary Medicine, Dentistry, or Food/Biotechnology Previous experience in pharmaceutical quality assurance Solid understanding of GDP/ GMP and pharmaceutical quality systems Previous experience in use of QMS (Trackwise would be ideal but open to others) Analytical, solutionoriented, and detailfocused working style Handson mentality with a strong sense of ownership and selfmotivation Strong [. .. ]
Job vor 8 Tagen bei Mindmatch.ai gefunden
Mundipharma
• AT- 9 Wien
[. .. ] CEE markets to ensure operational compliance. Issue Resolution and support the management of regional quality issues, including complaints, product recalls, and returns. Audit Management-Lead the preparation and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] support for internal and external GDP/ GMP audits and regulatory inspections. QMS Development-Maintain and evolve the Quality Management System in accordance with EU GDP/ GMP guidelines and national legislation. Quality Controls-Manage deviations, CAPAs, change controls, and conduct thorough quality risk assessments. Oversee technical documentation Quality/ Technical Agreements, pharmaceutical licenses, and ensure [. .. ] to monthly reviews and Product Quality Reviews (PQRs) . Compliance Monitoring-Conduct self-inspections and manage NMVO alerts and related regional contracts. Act as a proactive interface for stakeholders, providing expert quality guidance and training compliance support to regional teams. What youll bring University degree in Pharmacy would be ideal but may be open to other Scientific Degrees in areas such as Chemistry, Biology, Human or Veterinary Medicine, Dentistry, or Food/Biotechnology Previous experience in pharmaceutical quality assurance Solid understanding of GDP/ GMP and pharmaceutical quality systems Previous experience in use of QMS (Trackwise would be ideal but open to others) Analytical, solutionoriented, and detailfocused working style Handson mentality with a strong sense of ownership and selfmotivation Strong [. .. ]
Job am 16.03.2026 bei Mindmatch.ai gefunden
NEVEON Executive Committee
Senior Expert Medical and Scientific Affairs (all genders)
• KI Kremsmünster
Overview We are not offering you a job, but rather we are offering you a workplace that feels like home at Greiner Bio-One. Senior
Expert Medical and Scientific Affairs (all [...]
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[...] genders) Location: Kremsmünster, AT, 4550 Employment Type: Permanent Responsibilities Support our colleagues with your clinical and scientific expertise and experience in clinical diagnostics, contributing to the clinical and scientific knowledge base for Greiner Bio-One products Support the Clinical Studies team with regard to study [. .. ] marketing and educational purposes Coordinate and respond to customer inquiries Collaborate with the R D team, Product Managers and Product Application Specialists Your Profile You have completed your studies in Medicine, Biomedical Analytics, Biochemistry, Pharmacy or a similar discipline. An advanced degree (Ph D) is a plus but not required. You have gained experience as a Specialist in Clinical Chemistry and Laboratory Medicine, ideally with experience and a publication track record in preanalytical research phase. You have significant experience in a clinical [. .. ] have excellent English skills (Level C1 preferred) as well as a very good working knowledge of MS Office. You enjoy finding new approaches and solutions as well as communicating with internal and external partners. Membership of international professional organizations such as IFCC and EFLM is preferred. Our Offer A collaborative environment where diverse voices are valued and respected. Opportunities for professional growth and development. Flexibility in how you approach your work and balance your responsibilities. A culture that supports curiosity, continuous [. .. ]
Job am 08.03.2026 bei Mindmatch.ai gefunden
AOP Health
• AT- 9 Wien
Homeoffice möglich
[. .. ] trends and generate insights for Global and Affiliate stakeholders. Serve as the global escalation point for complex inquiries in collaboration with vendors and Global Medical Affairs. Act [...]
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[...] as subject matter expert for compliance topics including Pharmacovigilance, Regulatory Affairs, and Data Privacy. Support and optimize digital MI solutions (e. g. , Veeva Med Inquiry) and ensure data governance standards. Deliver product, system, and process trainings to internal teams and external partners. Ensure inspection readiness and adherence to SOPs, industry codes, and internal compliance standards. Collaborate cross-functionally with Regulatory, PV, Legal, and Medical 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 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Medical Director-Psychiatry (m/w/d)
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] Director will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials. Serve [...]
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[...] as a medical expert during project delivery lifecycle. Provide therapeutic and medical expertise to business development activities. Essential Functions The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested. Medical Monitoring: # # Primarily serves as Global and/or Regional Medical Advisor on assigned projects. # # Serves [. .. ] # Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring. # # Provides medical and scientific advises to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. # # Attends and presents at bid defense meeting, as required. [. .. ] # # Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, plus a minimum of 5 years experience in clinical medicine. # # Specialty board certification # # Ideally, candidate will have a minimum 2 years clinical trials experience as an investigator or medical/ clinical expert in the Pharma, CRO, or Biotech industry. # # Ability to establish and maintain effective working relationships with co-workers, managers and [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Frankfurt, Hesse
Führungs-/ Leitungspositionen
[. .. ] provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested. They will participate in all aspects of medical science involvement on assigned trials, serve [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as a medical expert during the project delivery lifecycle, and provide therapeutic and medical expertise to business development activities. Essential Functions Primarily responsible for medical monitoring with input into medical strategy as requested. Medical Monitoring Primarily serves as Global and/or Regional Medical Advisor on assigned projects. Serves as Scientific Advisor and provides guidance [. .. ] for business development activities. Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring. Provides medical and scientific advice to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/ regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Attends and presents at bid defense meetings, as required. Participates in strategic business [. .. ] international travel. Qualifications Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, plus a minimum of 5 years experience in clinical medicine. Specialty board certification. Ideally, candidate will have a minimum 2 years clinical trials experience as an investigator or medical/ clinical expert in the Pharma, CRO, or Biotech industry. Ability to establish and maintain effective working relationships with co-workers, managers and clients. Strong communication, presentation and interpersonal skills, including good [. .. ]
Job am 13.03.2026 bei Jobleads gefunden
Medical Director-Peer Voice
Führungs-/ Leitungspositionen
P S L Group is a global organisation dedicated to putting information at the service of
medicine. The companies and people of the P S L Group aim to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] improve medical care by serving those who need it, those who provide it and those who seek to improve it. Our primary purpose is to help clients increase the effectiveness of activities pertaining to scientific communication, medical education [. .. ] medical education. We publish medical education across a wide swath of medical specialties, including: Cardiology General and Family Practice Hematology Oncology Ophthalmology Urology Objective The Medical Director will collaborate with internal and external experts to complete the following key tasks: Identify existing practice gaps and underlying unmet needs (15) Develop strategic needs assessments/ proposals that align these practice gaps and unmet needs with innovative solutions to address these needs (20) Create high-quality content for medical education activities that meet established [. .. ] Solid editorial (writing and editing) skills and capability to adapt editorial style based on the educational format and/or the target audience (physicians, nurses, pharmacists, and other healthcare professionals) . Expert at Microsoft Office, specifically Power Point and Word. Comfortable working in a fast-paced, constantly evolving work environment. Proven ability to effectively set priorities, manage multiple projects/ assignments in various stages of development, and meet timelines, all while maintaining high quality standards. Positive, upbeat personality who communicates concisely and clearly, [. .. ]
Job am 01.03.2026 bei Jobleads gefunden
• Lausanne, Waadt
Führungs-/ Leitungspositionen
[. .. ] develop and grow. Dont hesitate to connect with us during the recruitment process to learn more Position Summary As a Medical Director for Clinical Trial/ Research Safety [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] you will provide expert safety leadership and input to clinical development programs for nutritional solutions and therapeutics across the lifespan, and ensure safety compliance with regulatory frameworks applicable to pharma, medical nutrition and food for medical purposes (FSMP) . A Day in the Life of a Medical Director Safety Responsible for building safety assessments [. .. ] Monitoring Boards charters, aggregate safety reports (DSUR/ ASR where applicable) , and risk management plans; contribute to Safety Risk Management Team (SRMT) and signal review forums Coordinate the management of internal trial safety boards and committees Drive safety strategies and ensure safety compliance with applicable regulatory frameworks, in close collaboration with clinical development, data management, medical, scientific and regulatory affairs teams as well as trusted external providers for case processing Engage with key opinion leaders (KOLs) and investigators, to shape safety [. .. ] dotted line alignment to internal patient safety risk management governance frameworks What Will Make You Successful Medical degree, Md/Ph D, preferably with specialization in one of the following areas: internal medicine/ gastroenterology/ pediatrics/ clinical pharmacology. Swiss medical practice license is a plus At least 5 years experience in clinical research and safety, in development or operations (pharma, biotech, diagnostics, medtech, nutrition, or CRO settings) Experience and proven impact in leading safety management in complex clinical trials, including issue management and regulatory [. .. ]
Job am 14.02.2026 bei Jobleads gefunden
Senior Director Medical Affairs-Neurology
• Ulm, Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] Are Teva Were Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether its innovating in the fields of neuroscience and immunology or delivering [...]
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[...] high-quality medicine worldwide, were dedicated to addressing patients needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. Youll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. [. .. ] clinical, patient care, experience in Neurology. Five years pharmaceutical industry experience. Pharmaceutical industry experience in neurology. Experience in successfully developing strategy and executing medical plans, and in building professional external expert networks. Broad and good knowledge of drug development, clinical trial design, regulatory requirements, business development and life cycle management etc. SKILLS/ QUALIFICATIONS: Able to work in a changing and flexible environment with a strong patient focus and enterprise mindset. Experienced and adept at working collaboratively across different cross-functional teams [. .. ] pension scheme) . Function Medical Affairs Reports To Neuroscience lead, GMA Contact Sonia Buxeda Human Resources Already Working TEVA? If you are a current Teva employee, please apply using the internal career site available on Employee Central. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site Tevas Equal Employment Opportunity Commitment Teva Pharmaceuticals is [. .. ]
Job gestern bei Jooble gefunden
Merck Sharp Dohme Corp
• Rheinland- Pfalz Rheinland- Pfalz, DE
[. .. ] testing Plan, conduct, and evaluate in-house or outsourced in-vitro and in-vivo studies according to GLP guidelines, including toxicology, target animal safety, pharmacokinetics, metabolism, and residue depletion. Prepare [...]
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[...] expert reports, regulatory submissions and scientific presentations in English for authorities and internal stakeholders. Maintain and extend engagement with contract research organizations, external experts, and universities. Act as preclinical representative within international multidisciplinary project teams Your Qualifications Veterinary Medicine degree, including Ph D or comparable scientific credentials Experience in Research and Development, ideally in the international veterinary pharmaceutical environment Experience with managing animal studies, ideally under GLP Strong background and experience in pharmacology, metabolism and toxicology, including evaluation of active substances Precise, analytical, proactive and creative work approach to problem [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Miltenyi Biotec
Qualification Validation Expert (m f d) : Play a key role in our manufacturing transition
• Rheinisch- Bergischer Kreis; Regierungsbezirk Köln; Westfalen Koeln
For more than 35 years, we have been developing cutting-edge science and technology to empower biomedical research and personalized
medicine. We combine excellence from more than 60 disciplines in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] natural sciences, engineering, and informatics to make a significant contribution to biomedical sciences. We encourage a creative working environment driven by pioneering spirit to seek new horizons boldly envisioning the future and turning it into reality. Today, more than 5, 000 [. .. ] and compliance, you will prepare, maintain and manage qualification and validation documentation, including URS, risk assessments, IQ/ OQ plans, reports and SOPs. Acting as a trusted partner, you will advise internal subject matter experts on qualification and validation projects, propose pragmatic solutions and actively support their successful implementation. You will contribute to Gx P activities such as deviations, CAPAs and change control, while continuously enhancing qualification and validation-related processes. You will collaborate closely with internal stakeholders (e. g. IT, QA, QC, [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Argenta
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern
[. .. ] the veterinary and animal feed sectors require qualified support for the development and approval of their products. KLIFOVET Gmb H, part of the Argenta Group, is an [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] internationally recognised provider of expert services in the veterinary medicine and animal feed sector based in Munich. We support our customers from the idea, through development, to approval and beyond. Service for our customers determines our actions. Founded in 1997, we are considered a global leader in animal health product development; Argenta and Klifovet have been awarded multiple times as [. .. ] of final study report, statistical report, and raw data Data Base validation Budget responsibility for the QA activities within projects Support maintenance of QM System and continuous improvement Performance of internal and supplier audits Prepare, participate and CAPA management related to customer audits and inspections by competent authorities Your profile: University degree in veterinary medicine, pharmacy or a comparable science Ideally, qualification as auditor or training in quality assurance and/or quality management Able to be to familiarize yourself with new [. .. ]
Job vor 10 Tagen bei Jooble gefunden
Miltenyi Biotec
Manufacturing Expert Software (m f d)
• Rheinisch- Bergischer Kreis; Regierungsbezirk Köln; Westfalen Bergisch Gladbach, DE
For more than 35 years, we have been developing cutting-edge science and technology to empower biomedical research and personalized
medicine. We combine excellence from more than 60 disciplines in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] natural sciences, engineering, and informatics to make a significant contribution to biomedical sciences. We encourage a creative working environment driven by pioneering spirit to seek new horizons boldly envisioning the future and turning it into reality. Today, more than 5, 000 [. .. ] technical expertise in the design, configuration, testing, validation, and maintenance of MES workflows and electronic batch records, combined with excellent problemsolving and communication skills. The role involves close collaboration with internal and external stakeholders to build effective partnerships, ensuring compliance with c GMP requirements and Quality Management Systems. In this position, you will play a key role in delivering highquality, compliant manufacturing services to our clients. Drive MES excellence in a GMP environment by designing, configuring, testing, validating, and maintaining MES workflows [. .. ]
Job vor 11 Tagen bei Jooble gefunden
Bioagilytix
• Hamburg Hamburg, DE
[. .. ] Bio Agilytix, we are passionate about premier science and the impact it has on our world. Our team of highly experienced scientists and professionals deliver tailored services [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] for supporting new medicine breakthroughs with best-in-class bioanalytical services. We are tirelessly committed to our customers by being solution-oriented and deadline-driven. . . and we are growing. Our culture is fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. [. .. ] GDP, GLP, GCLP, GCP Independence, enthusiasm, openness, and adaptability Demonstrated effective communication skills The ability to inspire others to do their best work and drive results Excellent customer service skills (internal and external) Proficiency in both German and English is required Minimum Preferred Qualifications-Education/ Experience Bachelors degree in analytical chemistry, chemistry, biochemistry, biotechnology, or related field with not less than twelve (12) years experience in a scientific laboratory environment; or Masters degree in analytical chemistry, chemistry, biochemistry, biotechnology, or related [. .. ] GCLP, GCP The benefits of joining our team: Broad exposure to a wide variety of protein therapeutics (enzymes, gene cell therapy, multifunctional therapeutic, oncolytic virus) Access to a network of expert bioanalytical scientists to collaborate with and grow Continued development and growth, international sites exposure and contacts Exposure to cutting-edge bioanalytical technologies Permanent employment Subsidy for the public transport network/ professional ticket and company parking spaces Participation in company pension schemes and/or capital formation benefits Additional company health insurance [. .. ]
Job am 23.04.2026 bei Jooble gefunden
Biontech
Department Lead Scientific Communications
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
[. .. ] Phase I and early clinical studies, including: Manuscripts, abstracts, posters, and oral presentations for scientific congresses Ensure consistency, scientific rigor, and compliance with Good Publication Practice (GPP) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] , ICMJE, and internal SOPs. Partner closely with Clinical Development, Biostatistics, Translational Science, and Regulatory to ensure timely and accurate communication of early data. Scientific Communications for Late-Stage Development Commercialization Lead the scientific communication team supporting Phase II/ III and prelaunch/ launch activities, including: Global publication and congress strategy for pivotal and late-[. .. ] scientific communications, digital congress presence, plain language summaries, and data transparency initiatives. A Good Match: Education Advanced scientific or medical degree required (Ph D, Pharm D, MD, or equivalent) in life sciences, medicine, or a related field. Experience 10+ years of experience in scientific communications, medical writing, or related medical/ clinical roles within the biopharmaceutical industry. Previous experiences leading a Scientific Communications Department is necessary. Significant experience in large, international pharmaceutical companies, with exposure to global functions and matrix environments. Experience in a [. .. ] and lifecycle management Working cross functionally with Clinical Development, Medical Affairs, Regulatory, and Commercial. Skills Competencies Excellent leadership skills. Deep understanding of clinical development processes, evidence generation, and data interpretation. Expert knowledge of publication standards (GPP, ICMJE) , ethical guidelines, and relevant codes of practice. Strong scientific storytelling skills: ability to convert complex data into clear, impactful narratives for diverse audiences. Excellent written and verbal communication skills with meticulous attention to scientific accuracy and consistency. Strategic mindset with the ability to [. .. ]
Job am 23.04.2026 bei Jooble gefunden
Sartorius AG
• Unstrut- Hainich- Kreis; Thüringen Vogtei, DE
Sabbaticals Work-Life-Balance
[. .. ] savings accuracy with teams and challenge assumptions, being an active part of Procurement acceleration 2.0 Be the first-level support for category management on product costing, bridging with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] costing expert if necessary Support supplier negotiations on financial scenario Highlight, collect and value financial risks for documented risk management report What will convince us A successfully completed Master s degree in Finance, Business Administration, Controlling or related field Strong background in Controlling or Finance within an industrial or manufacturing environment, ideally [. .. ] we offer As a growing global life science company, stock listed on the MDAX, Sartorius offers a wide range of Benefits: Personal and Professional Development: Mentoring, leadership programs, Talent Talks, internal seminar offerings, coaching for managers Work life balance: Remote options, flextime, flexible work schedules, sabbaticals Attractive compensation: Vacation and holiday bonuses including pension benefits with a 35 hr. week, 30 vacation days Large, modern campus: Open office spaces, terraces, company restaurant with vegetarian and vegan options, cozy Italian bistro with [. .. ] and cultural backgrounds. About Sartorius Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment. Join our global team and become part of the solution. We are looking forward to receiving [. .. ]
Job am 22.04.2026 bei Jooble gefunden
Biontech
Director Market Access
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Führungs-/ Leitungspositionen
[. .. ] market access activities in Germany. The focus will be on our innovative oncology products and vaccines. In this role, you will combine leadership skills, strategic expertise, and [...]
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[...] close collaboration with internal and external stakeholders to ensure sustainable access to our therapies within the German healthcare system. You will be part of a dynamic, interdisciplinary team dedicated to shaping the future of medicine. Your Contribution: Strategic Responsibility for Market Access in Germany Development and implementation of the market access strategy for the German portfolio (oncology vaccines) . Management of AMNOG processes, including leading dossier preparation, benefit assessments, negotiation preparation, and execution. Responsibility for pricing strategies, price negotiations, and long-term price positioning within [. .. ] billing pathways, and remuneration logics. Close collaboration with KVs (regional associations of statutory health insurance physicians) , health insurance funds, and other stakeholders. Close cooperation with Governmental Affairs, especially regarding expert input for policy briefings and strategic positioning. Participation in committees and meetings with political stakeholders while contributing your expertise. Team Leadership and Internal Collaboration Leading and developing an interdisciplinary market access team. Close coordination with Medical Affairs, HEOR (Health Economics Outcomes Research) , Commercial, Regulatory Affairs, Marketing, and Governmental Affairs. [. .. ]
Job am 17.04.2026 bei Jooble gefunden
Sobi
• Regierungsbezirk Köln; Westfalen Köln, DE
[. .. ] Inclusion Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments Job Description The Medical Science Liaison (MSL) is a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] fieldbased scientific expert responsible for engaging healthcare professionals, clinical experts, and key external stakeholders in support of the agreed medical strategy for Tryngolza, an innovative therapy for Familial Chylomicronemia Syndrome (FCS) , with future potential in Severe Hypertriglyceridemia (s HTG) . This position can be based in Cologne, Düsseldorf, Dortmund, Münster, Trier, Koblenz, Bonn, [. .. ] Scientific Support Deliver scientific education to HCPs, centers, and relevant networks. Support the Medical Advisor in developing educational content, diseaseawareness programs, and scientific resources. Provide scientific training and support to internal teams (e. g. , commercial, patient access, field teams) to ensure accuracy, consistency and compliance. Support advisory boards, congress activities, and expert meetings. Deliver and support education initiatives following Medical Excellence quality standards. Clinical Research Evidence Generation Contribute to evidencegeneration activities including: Phase IIIb/ IV studies Investigatorinitiated research (ISS/ ISR) [. .. ] a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we cant change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Chapter 2
(Senior) Clinical Research Scientist-Digital Cardiology. . .
• Berlin Berlin, DE
[. .. ] Trial Oversight Oversee sponsor-side clinical operations and budgets across multi-centre studies in Europe and the U. S. Lead, execute, and monitor clinical trials in collaboration with CROs [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and internal research teams Ensure adherence to GCP and regulatory requirements across all research activities Contribute to protocol design, endpoint definition, and data interpretation alongside R D and data science teams Build and maintain strong relationships with investigators, study sites, and clinical partners Scientific Development Dissemination Draft and co-author scientific publications [. .. ] with technical R D teams to validate AI models and translate clinical findings into algorithmic improvements Provide clinical and scientific input to commercial and partnership activities as a trusted medical expert Ensure clinical context and thinking are embedded across all departments What Were Looking For Required: MD or Ph D in Medicine, Biomedical Sciences, or a related field Clinical or research experience in cardiology At least 2 years experience in clinical practice, research, digital health, or medical device development Strong understanding of clinical trial methodology and GCP Experience authoring and publishing scientific papers Excellent communication and writing skills for both clinical and [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
Director Translational Sciences (Oncology)
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
Jobticket
[. .. ] deep knowledge of and extensive experience with oncology, the role will drive the translational strategies for clinical development of oncology programs based on an integrated view of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the respective translational expert functions Responsible for bridging preclinical experimental data to translational strategies in the assigned programs to deeply integrate the mechanism of action to the clinical development plan (target engagement, pharmacodynamics endpoints, patient selection) and correlate with clinical outcomes Provide scientific, technologic and strategic guidance and hands-on contribution to biomarker programs accompanying clinical trials to drive the company s R D programs; experience in CDx development is a plus Coordinate biomarker related program activities with internal and external stakeholders and driving integration of services, technologies, and capabilities to ensure reaching of program goals Provide state of the art biomarker input in regulatory documents (clinical study reports, IND, BLA documentation) Analyzes, interprets and presents clinical biomarker data and draws scientifically valid conclusions that support and enable decision [. .. ] program lead in the biotech/ pharmaceutical industry Therapeutic knowledge and scientific accomplishments as evidenced by publications in peer reviewed journals in oncology or immune-oncology In depth understanding of translational medicine and biomarker mechanisms associated with immune-oncology and targeted therapies. Demonstrated experience with innovative assay development and proven ability to effectively troubleshoot and solve complex problems, experience in collaborating with external specialty laboratories Experience in working within interdisciplinary cross-functional teams with other key development functions (clinical lead, regulatory, biostatistics, [. .. ]
Job am 08.04.2026 bei Jooble gefunden
IQVIA
Local Pharmacovigilance Responsible Person-12 months contract (part-time)
• Regierungsbezirk Darmstadt; Hessen Frankfurt am Main, DE
[. .. ] consistency and compliance across regions. Develop and maintain global SOPs, templates, and guidance documents for assigned processes. Drive process improvements and harmonization initiatives in collaboration with cross-functional [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] teams. Provide expert advice and training to internal stakeholders on global PV processes. Additional Responsibilities: Prepare and maintain PSMFs and local annexes for Germany. Oversee development and negotiation of pharmacovigilance agreements for assigned clients. Act as EU QPPV for small clients, where applicable. Mentor and train team members on PV processes and regulatory requirements. Support audits and inspections at global and local levels. Qualifications: Education: Bachelor s degree in Life Sciences, Pharmacy, Medicine, or related field (advanced degree preferred) . Experience: Minimum 5 years in pharmacovigilance or drug safety within a pharmaceutical company or CRO. At least 3 years of experience in PV system management and regulatory compliance. Previous experience as LCPP or similar role in Germany strongly preferred. Knowledge: In-depth understanding [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Nucsai
Senior Software Engineer
• Berlin Berlin, DE
[. .. ] prostate cancer care through cutting-edge AI and medical imaging technology. Founded in 2024 by a multidisciplinary team of oncologists, AI researchers, and healthcare innovators, we re tackling [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] one of medicine s most pressing challenges: the growing demand for accurate, timely cancer diagnostics in the face of rising scan volumes and limited radiologist capacity. Our mission is to enhance diagnostic precision and expand access to expert-level prostate cancer screening, ultimately improving patient outcomes worldwide. The Opportunity Join our engineering team as a Full Stack Engineer and help build the next generation of medical imaging platforms. You ll work at the intersection of healthcare and technology, developing secure, scalable systems that directly impact patient care and [. .. ] monitoring, and rollback capabilities Scalable data architectures using SQL databases with smart indexing and caching strategies Monitoring, logging, and alerting systems that ensure reliability in clinical environments Seamless integrations between internal services and external healthcare systems (HL7, FHIR) Modern React frontends for clinical workflows and data management What You Bring 3+ years of full-stack engineering experience with shipped products that real users depend on Strong system design skills with experience architecting distributed systems and microservices Dev Ops expertise with Kubernetes, [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Biontech
Senior Director, Global Clinical Operations
• Regierungsbezirk Rheinhessen- Pfalz; Rheinland- Pfalz Mainz, DE
Führungs-/ Leitungspositionen
[. .. ] . Highly skilled at: strategic operational execution, effective communication with senior leadership as well as vendor stakeholder management. Your Contribution: Accountable for the continuous adaptation of clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] operations needs and internal departmental processes for the rapidly growing organizations within Bio NTech. Represents clinical operations in interaction with international collaborations with pharma partners and other collaboration partners. Actively driving Governance Vendor Oversight for the main Clinical Research Organizations (CROs) working for Bio NTech, running steering committees and control activities to ensure the required compliance. [. .. ] preferred (Masters, Ph D, MD, Pharm D) . Global clinical trial experience in all phases (phase I-IV) . Over 8 years experience directly managing people PMP or equivalent certification desirable. Experience Expert knowledge and experience working with global international guidelines (ICH-GCP) for the performance of Clinical Development Programs. Strong Compliance focus with Direct experience involved in addressing regulatory inspections or internal process audits. Involved in drafting/ reviewing responses to Health Authority and Ethics committee questions Over 15 years experience in pharmaceutical/ [. .. ] will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities. Inspired? Become part of #Team Bio NTech At Bio NTech, we are committed to advancing medicine through innovation while fostering a dynamic workplace that embraces diversity. Join us on our mission to address diseases with high medical needs like cancer and infectious diseases. Together, we can make a meaningful impact worldwide. Your Benefits: Bio NTech is committed to the wellbeing of our team members and offers a [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Teva Pharmaceutical Industries Ltd.
Senior Director Medical Affairs-Neurology
• Region Donau- Iller, Württemberg; Regierungsbezirk Tübingen; Württemberg Ulm, DE
Führungs-/ Leitungspositionen
[. .. ] Are Teva Were Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether its innovating in the fields of neuroscience and immunology or delivering [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] high-quality medicine worldwide, were dedicated to addressing patients needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You ll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, [. .. ] clinical, patient care, experience in Neurology. Five years pharmaceutical industry experience. Pharmaceutical industry experience in neurology. Experience in successfully developing strategy and executing medical plans, and in building professional external expert networks. Broad and good knowledge of drug development, clinical trial design, regulatory requirements, business development and life cycle management etc. SKILLS/ QUALIFICATIONS: Able to work in a changing and flexible environment with a strong patient focus and enterprise mindset. Experienced and adept at working collaboratively across different cross-functional teams [. .. ] pension scheme) . Function Medical Affairs Reports To Neuroscience lead, GMA Contact Sonia Buxeda Human Resources Already Working TEVA? If you are a current Teva employee, please apply using the internal career site available on Employee Central. By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your [. .. ]
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