Medical Trials Stellenangebote


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376 Jobs für Medical Trials


Stellenangebote Medical Trials Jobs


Job vor 7 Tagen bei StepStone gefunden Miltenyi Biotec B. V. Co. KG

Senior Clinical Scientist Clinical Drug Development (m f d)

• Bergisch Gladbach Homeoffice möglich [. .. ] treat hematological cancers, using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal [...]
MEHR INFOS ZUM STELLENANGEBOT[...] clinical trials on a global scale. Join our highly professional team in bringing new medicines to the market As a Senior Clinical Scientist in Clinical Drug Development, you will take on both strategic and operational responsibilities in advancing innovative therapies in autoimmune diseases, oncology, with a focus on advanced therapy medicinal products [. .. ] ensuring the generation of high-quality clinical data and supporting the preparation of regulatory submissions (e. g. , IND, CTA, BLA, MAA) . Close collaboration with cross-functional teams; including medical, regulatory, biometrics, operations, CMC, and safety; is essential, as is representing Clinical Development in internal and external settings. Next to this, you support the professional development of junior scientists and contribute to establishing team-wide standards, processes, and best practices You demonstrate comprehensive expertise across the clinical data lifecycleworking backwards [. .. ]

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Job vor 7 Tagen bei StepStone gefunden Miltenyi Biotec B. V. Co. KG Senior Project Manager-Drug Development (m f d) • Bergisch Gladbach Homeoffice möglich [. .. ] treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal [...]
MEHR INFOS ZUM STELLENANGEBOT[...] clinical trials on a global scale. Join our highly professional team in bringing new medicines to the market. Job Description As Senior Project Manager, you will support global drug development programs from early development through to worldwide regulatory approval. In this role, you will lead the cross-functional project management effort, ensuring [. .. ] focused on achieving key development milestones. Key Responsibilites: Lead global project management activities for assigned drug-development programs, ensuring coordinated execution across key functions such as clinical, regulatory, CMC, safety, medical, biostatistics, and operations. Develop and maintain integrated project timelines with clear critical-path awareness; track progress, manage risks, and ensure transparent communication of milestones and deliverables. Drive cross-functional alignment by coordinating interdependencies, facilitating efficient handovers, and ensuring that all functions meet their commitments within agreed timeframes. Identify and manage [. .. ]

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Job vor 7 Tagen bei StepStone gefunden Miltenyi Biotec B. V. Co. KG

Lead Medical Writer (m f d)

• Bergisch Gladbach Führungs-/ Leitungspositionen Homeoffice möglich [. .. ] treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal [...]
MEHR INFOS ZUM STELLENANGEBOT[...] clinical trials on a global scale. Join our highly professional team in bringing new medicines to the market. As a Medical Writer you are part of our Miltenyi biomedicine business and within the Clinical Development team. You will be responsible for the development and oversight of clinical and regulatory documents that support global drug development programs, including preparation, development, review, revision and finalization of clinical documents for submission to regulatory authorities. [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH Senior Expert Engineering Device Development (m/f/d) • SZ schwaz [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH

Senior Expert Engineering Device Development (m/f/d)

• B bregenz [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH Senior Expert Engineering Device Development (m/f/d) • AT- 5 salzburg- umgebung [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH Senior Expert Engineering Device Development (m/f/d) • K villach [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH Senior Expert Engineering Device Development (m/f/d) • L linz- land [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH Senior Expert Engineering Device Development (m/f/d) • Y steyr [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH Senior Expert Engineering Device Development (m/f/d) • W wels [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job gestern bei Mindmatch.ai gefunden Novartis Pharmaceutical Manufacturing GmbH Senior Expert Engineering Device Development (m/f/d) • kirchdorf an der krems [. .. ] as LCM of commercial products. Support device design development following the design control process and applicable regulatory framework Ensure components are delivered and controlled to the required [...]
MEHR INFOS ZUM STELLENANGEBOT[...] quality for clinical trials and commercial production. Support internal external audits on medical devices related matters and provide input to health authority questions. Bachelor, Master or Ph D degree in engineering or equivalent Preferably 5+ years of experience working in development of medical device and/or combination products; preferred in pharmaceutical area or similar Experience in developing plastic and metal components; tolerance analysis, modelling [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden Regional Medical Science Liaison Chronic Cough (mfd) • München, Bayern Abgeschlossenes Studium Abgeschlossene Ausbildung Der/ Die Regionale Medical Affairs Manager (MSL) (m/w/d) für die Region Ost (Rostock Berlin Dresden Fulda Wolfsburg) ist im Therapiegebiet Pneumologie mit Fokus auf Chronic Cough (chronischer Husten) die [...]
MEHR INFOS ZUM STELLENANGEBOT[...] entscheidende Schnittstelle von GSK zu nationalen und regionalen externen Experten. Er/ Sie verantwortet die Umsetzung der entwickelten medizinischen Strategie in seiner/ ihrer Region [. .. ] the Centers for Medicare and Medicaid Services (CMS) website at Key Skills Presentation Skills, Time Management, Clinical Research, Communication skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care Employment Type: Full-Time Experience: years Vacancy: 1 #J-18808-Ljbffr 73159343 [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden

Associate Medical Director/ Medical Director

• Frankfurt (Oder) , Brandenburg Führungs-/ Leitungspositionen [. .. ] Be part of a multidisciplinary and focused team, that works towards getting novel promising ADCs to patients with solid and hematological cancers. Be Part of Our Team [...]
MEHR INFOS ZUM STELLENANGEBOT[...] As an Associate Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full life-cycle development of our antibody-drug conjugates (ADCs) global clinical trials. You will lead all clinical aspects of clinical trials, provide support to the Clinical Trial Team (CTT) , ensure patient safety, and support the company in clinical development and in medical aspects of early development. You will be responsible for clinical trial execution and analysis and serve as a key [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden Manager Medical Science Liaison Oncology • München, Bayern Munich, Germany full time Job ID:10560 Responsibilities Act as a field medical expert, delivering continuous medical education to HCPs in Germany and gathering actionable insights to inform strategy. Build [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and maintain scientific partnerships with key opinion leaders, Cooperative Study Groups, medical associations, and research organizations in oncology. Develop and execute an Medical Science Liaison (MSL) Oncology strategy aligned with local and European medical affairs priorities. Build and expand relationships/ networks with key medical and scientific experts in the field of breast cancer and/or lung cancer. Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits) , assisting with patient enrollment, and ensuring smooth information exchange. Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies. Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing [. .. ]

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Job vor 9 Tagen bei Jobleads gefunden

Medical Science Liaison Rare Tumour-Austria (all genders)

• Wien Spring Works: Medical Science Liaison Rare Tumors Austria (all genders) Join to apply for the Spring Works: Medical Science Liaison Rare Tumors Austria (all genders) role at Merck Healthcare [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Work Your Magic with us Ready to explore, break barriers, and discover more? We know youve got big plans so do we Our colleagues [. .. ] and advance patient care. Act as primary liaison to investigators interested in developing and performing investigatorinitiated research. Collaborate with the Clinical Operations organization to enhance patient enrollment in companysponsored clinical trials by identifying appropriate clinical trial sites, supporting clinical trial awareness, and interacting with investigators in ongoing studies. Serve as medical lead and provide scientific support at medical congresses, support national and European medical booths staffing, participate and lead clinical support, and facilitate medical discussions at advisory boards and local scientific/ [. .. ]

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Job vor 11 Tagen bei Jobleads gefunden SVP Head of Inflammation Immunology (all genders) • München, Bayern Führungs-/ Leitungspositionen [. .. ] Direction Define and lead the scientific strategy for the therapeutic area, aligned with Evotecs R D and business objectives. Identify emerging opportunities based on scientific trends, competitive [...]
MEHR INFOS ZUM STELLENANGEBOT[...] landscape, and unmet medical needs. Champion the therapeutic areas vision internally and externally, ensuring scientific excellence and innovation. Own the R D budget and ROI for the therapeutic area, including internal projects and strategic collaborations. Prioritize and oversee early-stage R D initiatives, from target identification to preclinical development. Provide scientific leadership and collaborate [. .. ] in-depth subject matter expertise in the I I space Drug discovery experience from target ID to PDC of at least 10 years, exposure to planning of clinical development and trials up to Po Cs desirable Proven track record in progressing discovery-stage programs and strategic collaborations Experience in licensing, partnering, and external scientific representation Strong network and credibility in the I I field Skills Competencies Strategic and systems thinker with a future-oriented mindset Strong leadership and influencing skills in [. .. ]

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Job am 11.12.2025 bei Jobleads gefunden

Senior/ Medical Director (Ophthalmology)

• Hamburg Führungs-/ Leitungspositionen [. .. ] this role As part of our Ophthalmology team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. Key Responsibilities Expert Guidance [...]
MEHR INFOS ZUM STELLENANGEBOT[...] : Provide advanced medical input on study design, measurement strategies, and trial protocols, including safety sections and investigator brochures. Comprehensive Safety Oversight : Review safety data such as adverse events, labs, vital signs, ECGs, and clinical trial reports from a medical perspective. Regulatory Risk Support : Conduct senior-level medical reviews of individual cases, cumulative listings, PSURs, PBRERs, DSURs, and Risk Management Plans. Medical Monitoring Signal Detection : Serve as a medical monitor in trials, perform literature reviews, and contribute to signal detection and interpretation. Regulatory Document Contributions : Offer expert medical insight into regulatory submissions and safety-related documentation. Team Client Engagement : Mentor junior medical staff, support SOP/ tool development, and join Commercial Operations in client meetings and presentations. Qualifications Medical Qualifications : [. .. ]

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Job am 08.12.2025 bei Jobleads gefunden Global Head of Pharmacovigilance • München, Bayern Führungs-/ Leitungspositionen [. .. ] oncology drug products across clinical development and commercialisation phases. This leadership role is central to ensuring safe, compliant, and successful oncology drug development and to maximising patient [...]
MEHR INFOS ZUM STELLENANGEBOT[...] safety from clinical trials to post-marketing surveillance. This position will report to the Chief Medical Officer and either work on a hybrid basis from the company office in Germany or on a remote basis. Your mission Develop and execute the overall drug safety and pharmacovigilance (PV) strategy aligned with company and global regulatory requirements, especially for oncology assets. Oversee safety surveillance, signal detection, risk assessment, [. .. ]

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Job am 07.12.2025 bei Jobleads gefunden

SVP Head of Cardio-Renal Research (all genders)

• München, Bayern Führungs-/ Leitungspositionen [. .. ] Direction Define and lead the scientific strategy for the therapeutic area, aligned with Evotecs R D and business objectives Identify emerging opportunities based on scientific trends, competitive [...]
MEHR INFOS ZUM STELLENANGEBOT[...] landscape, and unmet medical needs Champion the therapeutic areas vision internally and externally, ensuring scientific excellence and innovation Own the R D budget and ROI for the therapeutic area, including internal projects and strategic collaborations Prioritize and oversee earlystage R D initiatives, from target identification to preclinical development Provide scientific leadership and collaborate with [. .. ] project deliverables with in-depth subject matter expertise for cardiorenal Drug discovery experience from target ID to PDC of at least 10 years, exposure to planning of clinical development and trials up to Po Cs desirable Proven track record in progressing discoverystage programs and strategic collaborations Experience in licensing, partnering, and external scientific representation Strong network and credibility in the cardiorenal field Skills Competencies Strategic and systems thinker with a futureoriented mindset Strong leadership and influencing skills in a matrix environment [. .. ]

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Job am 06.12.2025 bei Jobleads gefunden Oncology Medical Director-Clinical Strategy Trials Führungs-/ Leitungspositionen A leading biotech company in Austria is seeking a Medical Director to drive clinical strategy in oncology drug development. This role combines scientific expertise and hands-on impact to shape [...]
MEHR INFOS ZUM STELLENANGEBOT[...] patient outcomes. You will act as Medical Monitor, lead protocol development, and build strong global partnerships. The ideal candidate is a Medical Doctor with oncology experience and a strong background [. .. ]

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Job am 06.12.2025 bei Jobleads gefunden Executive CSO-Oncology Trials Strategic Leadership • Bern Führungs-/ Leitungspositionen A leading Swiss oncology research institute is seeking a Chief Scientific Officer (CSO) to lead the Clinical Science team. This role involves developing and implementing clinical trials, building partnerships [...]
MEHR INFOS ZUM STELLENANGEBOT[...] with the industry, and overseeing research innovations within Switzerland. The ideal candidate will have a medical or scientific background (Md/Ph D) , proven leadership experience, and fluency in English plus German and/or French. This is a unique opportunity to contribute significantly to the advancement of oncology research. #J-18808-Ljbffr 71756845 [. .. ]

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Job am 06.12.2025 bei Jobleads gefunden Chief Scientific Officer (CSO) Switzerland, 80 100 (Ref. 2605) - Member of the executive Board • Bern Führungs-/ Leitungspositionen [. .. ] the Executive Board role at Auriga Vision AG. Our client is the Swiss Cancer Institute (former SAKK) , a non-profit organization focused on the development and implementation [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of clinical trials in oncology based in Berne, Switzerland. As part of the teams expansion, we are looking for a Member of the executive Board. Responsibilities Leadership : Leading the Clinical Science team (Senior Scientific Director, Head of Clinical Development, Medical Science Liaison) , approximately 10 Clinical Scientists and Medical Advisors; active member of the Management Board for the Swiss organization, reporting to the CEO. Research Innovation : Translating projects into clinical trials; from study protocol to starting the clinical studies in Switzerland. Responsible for developing and implementing Investor Initiated Trials [. .. ]

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Job am 04.12.2025 bei Jobleads gefunden Lead Medical Director CVRm/Heart Failure • Basel, Basel- Stadt Führungs-/ Leitungspositionen [. .. ] provide meaningful improvement to patients. Roche is looking for an experienced and highly specialized individual to join the Cardiovascular, Renal, and Metabolism group. The role of the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Lead or Senior Medical Director will focus on guiding and shaping our cardiovascular outcomes strategy. To be successful in this role, you will need to have extensive experience in late stage drug development and managing large-scale clinical trials, including outcome studies, in particular we are looking for candidates with experience in heart failure programs. You will have strong collaboration with cross-functional teams, including clinical research, regulatory affairs, and medical affairs, to ensure the successful progression of treatments through the pipeline and into the market. The position would [. .. ]

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Job am 04.12.2025 bei Jobleads gefunden Medical Science Liaison Ophta Nord • München, Bayern Position Summary The Apellis Medical Science Liaison (MSL) is a fieldbased role focused on developing and maintaining peertopeer scientific relationships with key medical experts. This role will primarily support [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the Apellis ophthalmology program and is embedded in the Medical Affairs department. The MSL will collaborate with physicians and other health care professionals to support trial [. .. ] a proactive team player, flexible, and able to work in dynamic situations. Presentation Skills, Time Management, Clinical Research, Communication skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care Others Office is home based. Travel within region up to 75. Required travel to medical meetings, team meetings, and other group meetings (will require some weekends) . Benefits and Perks Apellis offers a comprehensive benefits package, flexible time off, summer and winter shutdowns, paid family leave, [. .. ]

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Job am 04.12.2025 bei Jobleads gefunden Senior Medical Director, CVRM Heart Failure Outcomes • Basel, Basel- Stadt Führungs-/ Leitungspositionen A global healthcare company is seeking a Lead or Senior Medical Director for its Cardiovascular, Renal, and Metabolism group in Basel, Switzerland. The role focuses on guiding cardiovascular outcomes [...]
MEHR INFOS ZUM STELLENANGEBOT[...] strategies and requires extensive experience in late-stage drug development and managing large-scale clinical trials. The ideal candidate will possess an MD, strong collaboration skills, and a deep understanding of cardiovascular diseases, clinical trial protocols, and regulatory requirements. Join us in making a global impact on healthcare. #J-18808-Ljbffr 71363994 [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Medical Trials pro Jahr?

Als Medical Trials verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Medical Trials Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 376 offene Stellenanzeigen für Medical Trials Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Medical Trials Jobs?

Aktuell suchen 36 Unternehmen nach Bewerbern für Medical Trials Jobs.


Welche Unternehmen suchen nach Bewerbern für Medical Trials Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Trials Stellenangebote:


  • Tigermed (22 Jobs)
  • Tubulis GmbH (22 Jobs)
  • Bio Talent (11 Jobs)
  • Astra Zeneca (10 Jobs)
  • Novartis Pharmaceutical Manufacturing GmbH (8 Jobs)
  • Evotec International GmbH (6 Jobs)


In welchen Bundesländern werden die meisten Medical Trials Jobs angeboten?

Die meisten Stellenanzeigen für Medical Trials Jobs werden derzeit in Bayern (56 Jobs), Nordrhein-Westfalen (44 Jobs) und Berlin (31 Jobs) angeboten.


Zu welchem Berufsfeld gehören Medical Trials Jobs?

Medical Trials Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.


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