26 Jobs für Medical Trials in Baden-Württemberg
Stellenangebote Medical Trials in Baden-Württemberg Jobs
Job vor 2 Tagen bei StepStone gefunden
ZEISS
• Aalen (Baden- Württemberg)
Beratungs-/ Consultingtätigkeiten
[. .. ] preparation and submission of regulatory documents to authorities Ensure compliance of all products throughout their lifecycle, from authorization to discontinuation and ensure regulatory compliance for product labeling [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and support clinical trials Lead efforts to obtain necessary approvals and licenses in various markets (e. g. , EU MDR, UK MDR) Integrate regulatory elements into business processes to minimize approval delays and rejections Maintain and update regulatory documentation related to Quality Management Systems and assess marketing claims BS/ MSc in Life Sciences, Engineering, Optics, Regulatory Affairs and/or related experience Strong experience in regulatory affairs and quality management, preferably in medical devices, ideally with experience in standalone or embedded medical device software and IEC 62304, or in pharma Understanding and proven track record working with notified bodies and regulatory authorities in Europe Strong knowledge of regulatory requirements and processes in relevant markets combined with advanced project management skills, time and budget [. .. ]
Job am 03.12.2025 bei Jobleads gefunden
Quality Assurance Regulatory Affairs Manager
• Baden- Württemberg
Consultant
Medical Devices QARA United States Europe Quality Regulatory Affairs Manager Class III Cardiovascular Devices Company Type: Clinical-stage medical device developer focused on structural heart therapies Were partnering with an [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] emerging German Med Tech company developing a catheterbased Class III implant for structural heart repair. The device targets a major unmet need in minimally invasive heart valve therapy and is on track for pivotal trials. The company is now hiring a QA/ RA Manager to take ownership of its Quality and Regulatory function. This is a hightrust role, reporting directly to the Managing Director, and acting as the Quality Management Representative and Person Responsible for Regulatory Compliance. Quality Management Lead daytoday QMS operations (ISO13485:2016, 21CFR [. .. ]
Job am 18.11.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
Our client global Leader in the Pharmaceutical Industry is looking for an experienced
Medical Science Liaison specialized in Oncology. The role will be based remotely (ideally from Stuttgart) with frequent [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] travelling at a regional level. Your activities will consist in establishing scientific collaborations within the medical/ scientific community engaging with healthcare providers medical societies and organizations throughout the area of Stuttgart. Among your activities: [. .. ] Oncology/ Hematology. Fluent German good professional English Car driving licence 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 69875149 [. .. ]
Job am 17.11.2025 bei Jobleads gefunden
Medical Science Liaison-South Germany and Austria
• Stuttgart, Baden- Württemberg
Medical Science Liaison-South Germany and Austria Nordberg Medical is a Swedish biotech company working at the forefront of biomaterial science to reverse functionality loss. With stateoftheart biomaterials, we produce and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] market innovative medical products that target structural imbalances associated with aging. In 2021 we received CE certification for our first [. .. ] strategies with actionable tactics. Developing and delivering comprehensive product education and medicalscientific information. Supporting Key Account Managers (KAMs) in identifying and engaging influential experts in the field, and supporting clinical trials while ensuring compliance with local regulatory guidelines. Qualifications Proven experience in Medical Affairs or Medical Science in the aesthetics or dermatology field. Expertise in developing and delivering medical training programs. Demonstrated ability to operate compliantly in a fieldbased role, effectively collaborating within both the medical and commercial organizations. Strong knowledge [. .. ]
Job am 17.10.2025 bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
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 postmarketing 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, [. .. ]
Job gestern bei Jobleads gefunden
PhD-position at the University of Ulm, Germany (ENDOTRAIN) (DC9)
• Ulm, Baden- Württemberg
[. .. ] at the Institute of Biomedical Engineering at the University of Ulm, Germany. We Offer You: A World-Class Environment: Access to a leading research environment specializing in hardware/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] software for medical wearables, translational endocrinology, and machine learning for medical time-series. Cutting-Edge Resources: Benefit from state-of-the-art High-Performance Computing (HPC) facilities, unique multimodal datasets, and advanced wearable technologies. Global Collaboration: Extensive technical and physiological training, and the opportunity to build a professional network through world-leading international [. .. ] of ENDOTRAIN, collaborating closely with an international network of clinical and technical experts across the ENDOTRAIN consortium. This includes mandatory secondments to maximize your practical exposure and network. Remote clinical trials, powered by continuous data from medical wearables, promise to unlock new insights into complex diseases. However, integrating and synchronizing diverse, high-volume datasets, from dynamic hormone profiles to wearable biosensors (heart rate, actigraphy, temperature) , is a significant hurdle. Data quality loss is manifold, threatening the validity of groundbreaking medical [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Heidelberg, Baden- Württemberg
[. .. ] Chemical Biology Services and Open Targets groups, benefitting from a range of multi-disciplinary expertise and technologies. Develop machine learning pipelines for extracting drug side effects from drug [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] labels, clinical trials, publications and other documents Investigate modern NLP methodologies and propose ideas for the implementation of data extraction methods and pipelines Apply language models to extract and map drug-related information from unstructured text, e. g. from the scientific literature, Clinical Trials. gov Implement and/or fine-tune different NLP models, [. .. ] family, child and non-resident allowances, annual salary review, pension scheme, death benefit, long-term care, accident-at-work and unemployment insurances Flexible working arrangements-including hybrid working patterns Private medical insurance for you and your immediate family (including all prescriptions and generous dental optical cover) Generous time off: 30 days annual leave per year, in addition public holidays Relocation packageincluding installation grant (if required) Campus life:Free shuttle bus to and from work, on-site library, subsidised on-site gym and [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Customer Experience Manager, South Germany Munich, Germany; Nuremberg, Germany; Stuttgart, Germany
• München, Bayern
[. .. ] are waiting. Are you ready to make the leap? Blueprint Medicines, a Sanofi Company, is a global biopharmaceutical company that seeks to improve and extend patients lives [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] by solving important medical problems, with a focus on allergy/ inflammation and oncology/ hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success, leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit and follow us on X (formerly Twitter; Blueprint Meds) and Linked In. Blueflex is our operating model which optimizes culture, productivity, flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility. Blueflex allows [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
• Tübingen, Baden- Württemberg
Beratungs-/ Consultingtätigkeiten
The Institute for Ophthalmic Research (IOR) , part of the Centre for Ophthalmology at the University
Medical Centre Tübingen, offers excellent infrastructure and a dynamic basic and clinical research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] environment. Led by Prof. Dr. rer. nat. Marius Ueffing, it closely collaborates with the University Eye Hospital under Prof. Dr. med. Karl Ulrich Bartz-Schmidt. The IOR focuses on uncovering causes of degenerative, inflammatory, neoplastic and vascular eye [. .. ] risk factors, multimodal diagnostics for personalized treatment, and innovative therapies for retinal degeneration. The Institute offers broad expertise in multi-omics, computational biology, pathophysiology, neurophysiology, pre-clinical studies, and clinical trials. National and international collaborations with academic and industry partners and participation in major funded projects ensure a high level of innovation and cooperation. For more information click here. Tasks Working with cell cultures Working on retinal organ cultures Preparing tissue sections and staining (e. g. HE, IHC) Carrying out molecular [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Customer Experience Manager, South Germany
• Nürnberg, Stuttgart, München, Bayern, Baden- Württemberg
[. .. ] are waiting. Are you ready to make the leap? Blueprint Medicines, a Sanofi Company, is a global biopharmaceutical company that seeks to improve and extend patients lives [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] by solving important medical problems, with a focus on allergy/ inflammation and oncology/ hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success, leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit and follow us on X (formerly Twitter; Blueprint Meds) and Linked In. Blueflex is our operating model which optimizes culture, productivity, flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility. Blueflex allows [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
• Mannheim, Baden- Württemberg
Flexible Arbeitszeiten Work-Life-Balance
[. .. ] Forschung aktiv mitzugestalten, ohne den Stress einer klassischen Klinik. Interessiert? Bewirb Dich jetzt und werde Teil eines Teams, das die Zukunft der Diabetes-Therapie prägt Desired Skills and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Experience Diabetes Medical Expert Medizin Pharmaindustrie Klinische Forschung Endokrinologie Interne Medizin Facharzt Clinical Research Experience Public Health ICH-GCP Clinical Research Interpersonal Communication Cardiovascular Disease Clinical Trials Clinical Research Physician Principal Investigator Investigator #J-18808-Ljbffr 71995669 [. .. ]
Job am 07.12.2025 bei Jobleads gefunden
Senior Clinical Trial Project Manager (m/f/d) 80 100
• GVV Müllheim- Badenweiler, Baden- Württemberg
[. .. ] regenold Gmb H Founded in 1994, regenold Gmb H is an international regulatory service provider with over 100 employees. We support clients worldwide in the development, approval [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and market access of pharmaceuticals, medical devices and in vitro diagnostics, cosmetics, food supplements and other healthcare products. We are looking for an individual as soon as possible who can take on an active and clientfocused consulting role. Responsibilities Setup of clinical trials on behalf of regenold clients, including: Vendor selection and qualification Clinical budget negotiation and vendor contracting on behalf of the sponsor Vendor oversight and performance management Clinical trial risk assessment Operational management of clinical trials for medicinal products and medical devices (incl. IVDs) : Management and oversight of CROs and [. .. ]
Job am 20.11.2025 bei Jobleads gefunden
• Baden- Württemberg
Jobticket
Senior QA Auditor (m/f/d) Clinical
Trials Responsibilities: Lead audits for clinical trials and
medical products to ensure compliance with Gx P and regulatory standards. Develop and implement audit [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] plans based on risk assessments and conduct internal process and vendor audits. Address and escalate serious clinical trial violations, ensuring timely resolution. Contribute to the development and maintenance of the Quality Management System (QMS) , focusing on [. .. ]
Job am 18.10.2025 bei Jobleads gefunden
Postdoctoral researcher for the Heidelberg Institute of Global Health (m/f/d)
• Heidelberg, Baden- Württemberg
Jobticket
[. .. ] wide variety of research, with foci being medication effectiveness, health services research, and population health issues. Methods used in the groups work include quasi-experimental techniques, descriptive epidemiology, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and randomized trials. The fellow will be expected to publish in high-impact peer-reviewed journals. The postdoctoral fellow will have the opportunity to supervise Ph D, Master and Dr. med (thesis as part of medical studies in Germany) students. The fellow will also have the opportunity to teach as part of the institutes Masters and doctoral program but will not be required or expected to do so. The salary is paid according to the German TV-L system (the salary agreement for public service employees) [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
GULP experts united
• Biberach, Baden- Württemberg
[. .. ] open-ended employment contract Good chances of being taken on by our business partners Tailored further training opportunities and free language courses A wide range of employee benefits [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Your tasks Medical care of test subjects Independent implementation of the medical measures defined in the study protocol (e. g. ECG registrations, measurement of pulse and blood pressure, continuous monitoring of vital parameters, etc. ) Collection and preparation of human samples (e. g. blood and urine) Preparation and cleaning work (workstations, equipment, consumables) [. .. ] g. ICH-GCP) and internal standard operating procedures Your profile Completed medical training as a nurse, medical assistant, physician assistant or comparable practical relevant professional experience Experience in conducting clinical trials with healthy volunteers and good knowledge of GCP or willingness to acquire this knowledge with us Confident handling of blood sampling techniques Experienced with PC programs (e. g. MS Office, Teams) Fluent German, good written and spoken English skills Team player with strong communication skills and good time management The [. .. ]
Job vor 8 Tagen bei Neuvoo gefunden
GULP experts united
Medical Assistant/ Study Operations (m/f/d)
• Biberach, Baden- Württemberg
For a renowned pharmaceutical company based in Biberach, we are currently looking for a committed personality as
Medical Assistant/ Study Operations (m/f/d) part-time 50. Heres what we offer Attractive [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] salary and long-term job security through group affiliation Up to 30 days vacation per year Contribution to company pension scheme after end of probationary period Extensive social benefits, including Christmas and vacation bonuses Reimbursement of [. .. ] and free language courses A wide range of employee benefits Your tasks n this challenging and exciting role, you will take on a medical-clinical assistant function and accompany clinical trials from preparation to implementation. You will look after test subjects, independently carry out medical procedures such as ECG recording and vital parameter measurements, collect and process human samples and ensure the monitoring and safety of study participants. With your high quality standards, you will actively contribute to the success of [. .. ]
Job vor 13 Tagen bei Neuvoo gefunden
Astra Zeneca
• Baden- Württemberg
Führungs-/ Leitungspositionen
[. .. ] expands AZs cell therapy footprint in oncology by building patient-centered service lines and leading complex engagements with site leadership and frontline providers. It delivers operational and clinical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] guidance for trials and commercial products, leads site activation, and provides ongoing operational, quality, and clinical oversight post-activation. The TOM is a field, regional role reporting to a Regional Operations Director (ROD) . We are looking for a Cell Therapy Territory Operations Manager/ Regional Cell Therapy Operations Lead (m/f/d) Your [. .. ] market. Act as Subject Matter Expert (SME) influencing strategy, governance, and cross-functional execution at local and multi-country levels. Partner with internal teams (Program Management, QA, Manufacturing, Supply Chain, Medical Affairs, Market Access, Compliance, Sales/ Marketing) . Site Engagement Service Lines Build and maintain strong relationships with treatment centers and external partners (PIs, physicians, nursing, apheresis, cell therapy labs) . Establish patient-centered service lines and operational standards. Operational Excellence Ensure compliance with regulatory/ accreditation standards (, FACT) ; maintain [. .. ]
Job am 05.12.2025 bei Neuvoo gefunden
Universitätsklinikum Heidelberg
Postdoctoral researcher for the Heidelberg Institute of Global Health (m/f/d)
• Heidelberg, Baden- Württemberg
Jobticket
[. .. ] wide variety of research, with foci being medication effectiveness, health services research, and population health issues. Methods used in the groups work include quasi-experimental techniques, descriptive epidemiology, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and randomized trials. The fellow will be expected to publish in high-impact peer-reviewed journals. The postdoctoral fellow will have the opportunity to supervise Ph D, Master and Dr. med (thesis as part of medical studies in Germany) students. The fellow will also have the opportunity to teach as part of the institutes Masters and doctoral program but will not be required or expected to do so. The salary is paid according to the German TV-L system (the salary agreement for public service employees) [. .. ]
Job am 01.12.2025 bei Neuvoo.com gefunden
Barrington James
• Mannheim
[. .. ] an experienced Principal Investigator to lead and oversee diabetes and endocrinology clinical studies. This position is ideal for a physician with a strong background in conducting Phase [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] II to IV trials and hands-on experience with Type 1 or Type 2 diabetes populations. Act as Principal Investigator for diabetes and endocrine clinical trials, ensuring full compliance with GCP Provide medical oversight and safety assessment for all study participants Supervise study teams including Sub Investigators, Study Nurses and Coordinators Review and sign off eligibility assessments, adverse events, patient histories and study documentation Participate in monitoring visits, audits and sponsor or CRO meetings Collaborate closely with site leadership to optimise recruitment, retention [. .. ]
Job am 27.11.2025 bei Neuvoo.com gefunden
wax.
Senior Regional Medical Advisor-Rare Disease (Central/ South)
• Stuttgart
Our client has a fantastic opportunity for a Senior
Medical Science Liaison (MSL) / Regional Medical Advisor to join the Medical team. This role will focus on the Central/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Southern part of Germany. This role will support their portfolio of products and relay field-based clinical/ medical insights in order to support the future strategy. This position will provide operational support for activities related to Medical Information and Communication, Medical Education and Training, Investigator Initiated Trials, Key Opinion Leader outreach bringing value via scientific exchange. The position will also provide Research Clinical Development support as needed. The RMA will support the Medical Director in all aspects, i. e. representation of company in scientific presentations, conferences, and support for the Commercial Organisation while ensuring compliance with all [. .. ]
Job am 20.11.2025 bei Neuvoo.com gefunden
Tigermed
Contractor CRA-Tigermed Jyton-Germany (MJ000035)
• Stuttgart
[. .. ] all studies. Conduct monitoring visit according to monitoring plan and SOP; address issues with sites and complete monitoring visit report in a timely manner. Ensure timely coordination [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of study materials (medical device, IVD, drug, non-drug, equipment) to the site for start-up and throughout the study. 2. Training Provide ongoing training to site staff with regards to GCP, study protocol and requirements. Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. [. .. ] processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 70064668 [. .. ]
Job am 20.11.2025 bei Neuvoo.com gefunden
Tigermed
Contractor PM-Tigermed Jyton-Germany (MJ000034)
• Stuttgart
1. Job Purpose To implement project management of clinical
trials effectively, and to ensure success of clinical trials. 2. Responsibilities Make the project management plan: To draft and implement [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] feasible project management plan according to SOPs, ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure the trial in managed under the project management plan. Make monitoring plan: To draft and [. .. ] Manage site feasibility, site selection, initiation, monitoring, and close-out activities. Client Maintenance: Keep positive relationship with sponsor and investigator. 3. Minimum Qualifications a Academic/ Major: Bachelor degree or above in Medical, Pharmacology or Biology related majors. b) Professional Skills Adequate knowledge of medical device development, including local regulation, GCP. GCP certificate required. (c) Working Experience At least 5 years clinical trial experience, at least 3 years of independent project management experience. Experience of at least 3 medical device clinical trials. (d) [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Clinical Scientist-Manager/ Senior Manager (m/f/d)
• Stuttgart
[. .. ] (m/f/d) 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
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>trials. You will support the review, analysis, and interpretation of clinical trial data, contribute to the development of critical clinical trial documents, and take an active role in risk monitoring and mitigation. You will be part of a highly collaborative and cross-functional team involved with site evaluation, study start-up, [. .. ] close-out of our trials. This position will report to the VP, Clinical and Translational Development and will be based in Munich or remotely in Germany. Your mission Support the
Medical Director in the oversight of clinical studies including review and interpretation of clinical trial data and timely execution of deliverables in collaboration with relevant internal and external partners. Take a lead role in writing protocol amendments, informed consents, and other protocol-related documents for the operational execution of clinical studies. [. .. ]
▶ Zur Stellenanzeige
Job am 14.10.2025 bei Neuvoo.com gefunden
Tubulis GmbH
Associate Medical Director/ Medical Director
• Stuttgart
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 [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Tigermed
Contractor CRA-Tigermed Jyton-Germany
• Stuttgart
[. .. ] all studies. Conduct monitoring visit according to monitoring plan and SOP; address issues with sites and complete monitoring visit report in a timely manner. Ensure timely coordination [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of study materials (medical device, IVD, drug, non-drug, equipment) to the site for start-up and throughout the study. 2. Training Provide ongoing training to site staff with regards to GCP, study protocol and requirements. Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements. [. .. ] processes/ procedures. Good working and proactive attitude. Ability to work in team. 3. Working Experience: At least 2 years of CRA experiences. Experience in at least 3 medical device clinical trials. 4. Language ability: Good written and oral English. 5. Computer: Proficient Microsoft Word, Excel, PPT and Outlook, etc 6. Other abilities such as Communication skills Information-gathering skills Knowledge and/or experience in medical practice is a plus. 65935218 [. .. ]
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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 in Baden-Württemberg bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 26 offene Stellenanzeigen für Medical Trials Jobs in Baden-Württemberg.
Wieviele Unternehmen suchen nach Bewerbern für Medical Trials Jobs in Baden-Württemberg?
Aktuell suchen 10 Unternehmen nach Bewerbern für Medical Trials Jobs in Baden-Württemberg.
Welche Unternehmen suchen nach Bewerbern für Medical Trials Stellenangebote in Baden-Württemberg?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Trials Stellenangebote in Baden-Württemberg:
- Tigermed (3 Jobs)
- GULP experts united (2 Jobs)
- Tubulis GmbH (2 Jobs)
- ZEISS (1 Job)
- Astra Zeneca (1 Job)
Zu welchem Berufsfeld gehören Medical Trials Jobs in Baden-Württemberg?
Medical Trials Jobs in Baden-Württemberg gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
