Medical Trials Stellenangebote


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406 Jobs für Medical Trials


Stellenangebote Medical Trials Jobs


Job vor 3 Tagen bei StepStone gefunden Randstad Deutschland GmbH Co. KG

Compliance Specialist (f/m/d)

• Penzberg Angebote von Zeitarbeitsunternehmen [. .. ] is your lucky day Our subsidiary Randstad professional solutions has a vacant position as compliance specialist at the pharmaceutical company Roche in Penzberg. Tariff-based wages, care by [...]
MEHR INFOS ZUM STELLENANGEBOT[...] a company medical center, and employee discounts-all advantages that you can count on with Randstad. Its best to apply online right away and secure this job Applications from individuals with disabilities are warmly welcome. Support Gx P compliance of all activities in the clinical trial supply management, drug-related distribution and storage Responsibility for the project-related Gx P documentation and maintenance of lists Operational support and independent performance of operational tasks as process expert in the IMP Gx P Compliance Team across diverse clinical trials and R D Programs (e. g. Batch Record Reviews and TMF Filing) Establish and maintain inspection readiness for clinical trial supply activities and support in preparing, accompanying and following up on audits and inspections Optimization of processes and workflows (e. g. support in the creation and review of SOPs and [. .. ]

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Job vor 5 Tagen bei StepStone gefunden Milteny GmbH 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 5 Tagen bei StepStone gefunden Milteny GmbH

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 5 Tagen bei StepStone gefunden Milteny GmbH 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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Neu Job vor 4 Std. bei Stellen-Online gefunden Link Medical

Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) / (Sr) CRA at LINK Medical (DE) - Vollzeit

• 10783, Berlin Führungs-/ Leitungspositionen About us As LINK Medical continues to grow, we currently have an open position at our office in Berlin (DE) LINK Medical is searching for a highly motivated Local Regulatory [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Contact Study Start-Up (SSU) / Regulatory Lead (Clinical Studies) / (Sr) CRA in Germany. As a Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) [. .. ] study submissions. Provide guidance (internal and external) on regulatory requirements. Optional (dependent on previous experience) : Contribute to and coordinate regulatory and EC clinical study application submissions for multi country trials (including submissions for Clinical Trials with IMPs via CTIS) . If applicable also work partly as CRA including:Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ ISO 14155, SOPs, and regulations. Serve as main point of contact with the study site. Perform Source Data Review [. .. ]

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Neu Job vor 4 Std. bei JobMESH gefunden Link Medical Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) / (Sr) CRA at LINK Medical (DE) • State of Berlin 10783 Führungs-/ Leitungspositionen About us As LINK Medical continues to grow, we currently have an open position at our office in Berlin (DE) LINK Medical is searching for a highly motivated Local [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Regulatory Contact Study Start-Up (SSU) / Regulatory Lead (Clinical Studies) / (Sr) CRA in Germany. As a Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) [. .. ] study submissions. Provide guidance (internal and external) on regulatory requirements. Optional (dependent on previous experience) : Contribute to and coordinate regulatory and EC clinical study application submissions for multi country trials (including submissions for Clinical Trials with IMPs via CTIS) . If applicable also work partly as CRA including:Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ ISO 14155, SOPs, and regulations. Serve as main point of contact with the study site. Perform Source Data Review [. .. ]

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Neu Job vor 4 Std. bei JobMESH gefunden Link Medical

Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) / (Sr) CRA at LINK Medical (DE)

• State of Berlin 10783 Führungs-/ Leitungspositionen About us As LINK Medical continues to grow, we currently have an open position at our office in Berlin (DE) LINK Medical is searching for a highly motivated Local [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Regulatory Contact Study Start-Up (SSU) / Regulatory Lead (Clinical Studies) / (Sr) CRA in Germany. As a Local Regulatory Contact SSU/ Regulatory Lead (Clinical Studies) [. .. ] study submissions. Provide guidance (internal and external) on regulatory requirements. Optional (dependent on previous experience) : Contribute to and coordinate regulatory and EC clinical study application submissions for multi country trials (including submissions for Clinical Trials with IMPs via CTIS) . If applicable also work partly as CRA including:Monitor and manage clinical trials (phases I-IV) in compliance with protocol, ICH-GCP/ ISO 14155, SOPs, and regulations. Serve as main point of contact with the study site. Perform Source Data Review [. .. ]

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Job vor 3 Tagen 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 vor 6 Tagen 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 vor 7 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 8 Tagen 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 vor 10 Tagen 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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Job vor 10 Tagen 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 vor 10 Tagen 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 vor 10 Tagen bei Jobleads gefunden

Lead Medical Director CVRm/Heart Failure

• Basel, Basel- Stadt Führungs-/ Leitungspositionen Lead Medical Director CVRm/Heart Failure page is loaded # # Lead Medical Director CVRm/Heart Failurelocations: Basel: Welwyntime type: Full timeposted on: Posted Todayjob requisition id: 202512-130862At Roche you can [...]
MEHR INFOS ZUM STELLENANGEBOT[...] show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine [. .. ] 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 vor 10 Tagen bei Jobleads gefunden Medical Director, CV Outcomes Heart Failure • Basel, Basel- Stadt Führungs-/ Leitungspositionen A global healthcare company is seeking a Lead Medical Director based in Switzerland to guide cardiovascular outcomes strategy. Ideal candidates will have a background in cardiology, extensive experience in [...]
MEHR INFOS ZUM STELLENANGEBOT[...] late-stage clinical trials, and the ability to collaborate across various teams. Responsibilities include providing critical insights for project development and mentoring other professionals within Roche. This role offers the opportunity to contribute to meaningful advancements in healthcare. #J-18808-Ljbffr 71364304 [. .. ]

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Job vor 11 Tagen 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] an 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 [. .. ]

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Job vor 11 Tagen bei Jobleads gefunden Country Medical Director (Austria) (wmd) • Wien Führungs-/ Leitungspositionen [. .. ] aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche where every voice matters. The [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Position Our Country Medical Director (CMD) drives scientific medical and clinical excellence and innovation through strategic leadership strong crossfunctional interactions and continuous engagement with the scientific community and key health care ecosystem this role you ensure medical compliance and superior patient outcomes while fostering a high performance culture and continuous professional development of the [. .. ] excellent command of German and English Key Skills EMR Systems Post Residency Experience Occupational Health Experience Clinical Research Managed Care Primary Care Experience Medical Management Utilization Management Clinical Development Clinical Trials Leadership Experience Medicare We offer an annual salary starting from 120000 complemented by an attractive benefits package. This includes a competitive bonus scheme participation in our stock program pension contributions and more. Depending on your qualifications and experience a higher compensation is possible. You will also join an innovative and [. .. ]

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Job vor 12 Tagen bei Jobleads gefunden Associate Medical Director/ Medical Director Führungs-/ Leitungspositionen Associate Medical Director/ Medical Director About Us The development of novel, effective and safe therapies for the treatment of cancer is one of the main challenges for modern medicine. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] We want to drive this process forward. The main goal of Tubulis is to become a leading company in the field of targeted [. .. ] Medical Director/ Medical Director and member of our Clinical Development team, you will support the planning and execution of full lifecycle 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 am 24.11.2025 bei Jobleads gefunden Senior Director Medical Affairs (mfd) • Wien Führungs-/ Leitungspositionen Homeoffice möglich [. .. ] We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is realized. We engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to [. .. ] date. Required Experience : Exec Key Skills : EMR Systems, Post Residency Experience, Occupational Health Experience, Clinical Research, Managed Care, Primary Care Experience, Medical Management, Utilization Management, Clinical Development, Clinical Trials, Leadership Experience, Medicare Employment Type : Full-Time Experience : years Vacancy : 1 #J-18808-Ljbffr 70394789 [. .. ]

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Job am 23.11.2025 bei Jobleads gefunden Medical Science Liaison Manager, Nephrology, South • München, Bayern This is what you will do: The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexions product/ s across [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the product/ s life cycle. He/ she is a peer scientific expert who communicates accurate and applicable science to Key Opinion Leaders (KOLs) within a geographic area. He/ [. .. ] with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage [. .. ]

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Job am 23.11.2025 bei Jobleads gefunden Medical Science Liaison Manager, Nephrology, North-West • München, Bayern This is what you will do: The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexions product/ s across [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the product/ s life cycle. He/ she is a peer scientific expert who communicates accurate and applicable science to Key Opinion Leaders (KOLs) within a geographic area. He/ [. .. ] with up-to-date medical and scientific information Identify and execute collaboration opportunities between expert KOLs in nephrology and Alexion medical affairs and clinical development such as publications, investigator-initiated trials, regional advisory boards, training and speaker development programs. Communicate experts opinion, feedback on new data and clinical trends to Alexion Medical Affairs, therapeutic area (TA) franchises and translate this information into strategic recommendations to enhance science and advance patient care. Respond to unsolicited medical information requests in the region, manage [. .. ]

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Job am 21.11.2025 bei Jobleads gefunden Principal Technical Marketing Engineer • München, Bayern [. .. ] tickets. Serve as a trusted technical advisor and subject matter expert (SME) , building strong relationships with customers, partners, and internal teams to support proofs of concept [...]
MEHR INFOS ZUM STELLENANGEBOT[...] (Po Cs) , trials, and sales enablement initiatives. Develop and deliver advanced technical training and enablement content for Systems Engineers, Channel Partners, and Field Teams to strengthen technical acumen and ensure market alignment. Act as the voice of the customer (Vo C) during product testing and evaluation, ensuring new features align with evolving market and [. .. ] Alto Networks is an equal opportunity employer. We celebrate diversity in our workplace, and all qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy) , sexual orientation, or other legally protected characteristics. All your information will be kept confidential according to EEO guidelines. #J-18808-[. .. ]

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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 406 offene Stellenanzeigen für Medical Trials Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Medical Trials Jobs?

Aktuell suchen 34 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:


  • Tubulis GmbH (22 Jobs)
  • Planet Pharma (11 Jobs)
  • wax. (11 Jobs)
  • Tigermed (11 Jobs)
  • Bio Talent (11 Jobs)
  • Astra Zeneca (10 Jobs)


In welchen Bundesländern werden die meisten Medical Trials Jobs angeboten?

Die meisten Stellenanzeigen für Medical Trials Jobs werden derzeit in Bayern (53 Jobs), Nordrhein-Westfalen (47 Jobs) und Berlin (31 Jobs) angeboten.


Zu welchem Berufsfeld gehören Medical Trials Jobs?

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


Weitere Job-Ideen!
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