25 Jobs für Clinical Trials Specialist
Stellenangebote Clinical Trials Specialist Jobs
Job vor 11 Tagen bei Mindmatch.ai gefunden
team2work
• W wien
[. .. ] Tierarzneimitteln, uvm. vorweisen kann und auch laufend innovative, therapeutische Lösungen entwickeln und damit zur Verbesserung der Gesundheit und der Lebensqualität betroffener Menschen beitragen, suchen wir ab Jänner [...]
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[...] 2026 Regulatory Affairs Specialist m/w/d Clinical Trials Applications (CTAs) : Unterstützung bei der Einreichung, Bewertung und Genehmigung von klinischen Studienanträgen gemäß EU-CT-Verordnung Funktion als Clinical Point of Contact im österreichischen RA-Team in enger Zusammenarbeit mit dem lokalen Clinical Trials Team Regulatorisches Umfeld: Aktuelle Kenntnis lokaler und internationaler Gesetze und Richtlinien Teilnahme an Konsultationen zu [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology)
• Hamburg
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
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[...] resourcing and Functional Service (FSP) solutions. About 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 : Provide advanced medical input on study design, [. .. ] 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 : Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise : Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge : Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation and internal SOPs. Adaptability : Comfortable working in fast-[. .. ]
Job am 04.12.2025 bei Jobleads gefunden
• München, Bayern
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes full service-capabilities, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] resourcing and Functional Service (FSP) solutions. About 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 : Provide advanced medical input on study design, [. .. ] 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 : Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise : Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge : Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation and internal SOPs. Adaptability : Comfortable working in fast-[. .. ]
Job am 27.06.2025 bei Jobleads gefunden
Senior/ Medical Director (Ophthalmology) 0.5 FTE
Führungs-/ Leitungspositionen
[. .. ] Senior/ Medical Director (Ophthalmology) , 0.5 FTE. TFS Health Science is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout [...]
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[...] their clinical development journey. Join our team as a Senior/ Medical Director (Ophthalmology) . The Senior/ Medical Director is a key member of the Project Delivery team, working independently to manage safety and medical matters in line with company policies, standard operating procedures (SOPs) , and regulatory requirements. With deep medical expertise, [. .. ] 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: Medical Doctor (MD) with specialist medical training in Ophthalmology and at least 5 years experience in clinical practice. Clinical Trial Expertise: Experience serving on safety data review boards or equivalent roles in clinical research. Regulatory Knowledge: Strong understanding of GCP, ICH guidelines, pharmacovigilance legislation, and internal SOPs. Adaptability: Comfortable working in fast-paced environments with [. .. ]
Job gestern bei Jobleads gefunden
• Stuttgart, Baden- Württemberg
[. .. ] to developing and delivering life-changing medicines for people with severe rare diseases and cancer. The company has a diversified targeted oncology pipeline spanning solid tumors and hematological [...]
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[...] cancers, including clinical trials in rare tumor types and highly prevalent, genetically defined cancers. Their strategic approach and operational excellence in clinical development have enabled it to rapidly advance its lead product candidates into late-stage trials and enter into multiple collaborations with innovators in industry and academia to unlock the full potential for its portfolio and create more solutions for patients with cancer. As a Therapeutic Area Specialist (TAS) , you will play a critical role in expanding the companys presence through a complementary sales approach. You will work independently and in close coordination with your regional partner to engage diagnosing and referring healthcare professionals (HCPs) , build local networks, and increase disease awareness to generate patient leads. [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Clinical Applications Specialist
• Frankfurt, Hesse
Clinical Applications
Specialist Join to apply for the Clinical Applications Specialist role at Tera Recon, Inc. Company Overview Concert AI is at the forefront of revolutionizing healthcare with our [...]
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[...] cuttingedge AI and data solutions. Our mission is to accelerate insights, advance research, and improve patient outcomes in oncology and across life sciences. As a [. .. ] solution provider for AIempowered radiology, oncology, cardiology, neurology, and vascular surgery. In the future, the combination with Concert AI could bring a single, advanced AIaugmented diagnosis and interpretation capability from clinical trials to patient care. Learn more about Tera Recon at, or follow us on Linked In. EEO Concert AI provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Admont, Steiermark
Clinical Specialist AWC (m/f/) Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and [...]
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[...] help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided [. .. ] hospital standards. Deliver handson training and inservices for nurses, wound care teams, surgeons, physicians, and allied staff on appropriate product selection and correct application. Provide onsite/ remote clinical support during trials, conversions, and golives to ensure safe and effective use. Build trusted relationships with key stakeholders: wound care nurses/ specialists, tissue viability teams, surgeons, diabetology/ vascular teams, procurement, pharmacy/ materials management, and hospital quality teams. Support the development and delivery of educational materials: protocols, dressing guides, competency checklists, and clinical FAQs. [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Tenure Track Position according to 99 (5) Universities Act for Immune-mediated kidney disease. . .
[. .. ] programme Is the Job related to staff position within a Research Infrastructure? No Offer Description Tenure Track Position according to 99 (5) Universities Act for Immune-mediated kidney [...]
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[...] diseases and clinical autoimmunity at the Department of Internal Medicine IV of the Medical University of Innsbruck (full-time position) The Medical University of Innsbruck, located in the heart of the Austrian Alps, is the largest and most important medical research and education facility in the West of Austria. We currently teach and [. .. ] the basis of a positive evaluation, the contract is converted into an employment contract for an indefinite period. Your profile Ph D or comparable qualification relevant to the field a completed specialist training in internal medicine and nephrology, meeting the requirements for acceptance into the list of medical doctors of the Austrian Medical Association excellent research and publication activity in nephrology and autoimmunity experience in the conception and acquisition of third-party funded research projects academic teaching experience as well as the [. .. ] to participate in interdisciplinary and translationally oriented research potential to head an independent scientific research group experience in the field of immune-mediated kidney diseases with a focus on clinical trials international scientific visibility (e. g. through international presentations) German and English language skills, minimum level B2 according to the European reference framework Desired international collaborations in the field of immune-mediated kidney diseases Your main task academic teaching and supervising students within the different university programs the establishment of a [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
[. .. ] in seven Bachelor-, Master-and Doctoral Programs, most of them in medicine. A dedicated staff of more than 2, 200 employees covers all relevant fields from basic research [...]
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[...] to clinical sciences. The successful applicant initially concludes an employment contract for a fixed term of six years and, following a positive outcome of the procedure, a qualification agreement. Once it has been established that the qualification agreement has been fulfilled on the basis of a positive evaluation, the contract is converted into an employment contract for an indefinite period. Your profile Requirements Ph D or comparable qualification relevant to the field completed specialist training in neurology, meeting the requirements for acceptance into the list of medical doctors of the Austrian Medical Association excellent research and publication activity in the specific research field experience in designing and acquiring third-party funded research projects university teaching experience and willingness to engage in teaching and further [. .. ] oriented research in the field of circadian rhythms potential to head an independent scientific research group experience in the field of sleep disorders experience in planning, conducting, and evaluating clinical trials close international networking in neurological sleep medicine and sleep research German language skills, minimum level B2 according to the European reference framework Your main task academic teaching and supervising students within the different university programs the establishment of a research group in the field of human sleep medicine and sleep [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Drug Safety Physician
• Wien
Lead Recruiter Meet Life Science Pharmacovigilance, Drug Safety
Clinical Operations
Specialist Drug Safety Physician (m/f/d) Employment Type: Permanent Join a leading international organisation dedicated to improving health outcomes [...]
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[...] worldwide. This privately owned global company develops and manufactures innovative therapies using advanced biological and biotechnological processes. With a strong commitment to scientific excellence and patient care, the organisation combines the [. .. ] research, and developmenthome to more than 1, 600 employees working to advance life-enhancing healthcare solutions. Your Main Tasks and Responsibilities Conduct medical evaluation of cases from spontaneous reports, clinical trials, and post-marketing surveillance in accordance with regulatory requirements and internal SOPs. Assess seriousness, listedness, and causality of individual case safety reports. Initiate and support timely safety-related analyses. Provide medical input for periodic safety reports (e. g. , PBRERs/ PSURs) and broader safety analyses. Contribute to the development and [. .. ]
Job am 06.12.2025 bei Jobleads gefunden
• München, Bayern
Sponsor Dedicated Start up
Specialist based in Germany Principal Talent Acquisition Partner DACH at Fortrea/ Driving Data-Driven Talent Strategies/ Stakeholder Engagement/ DEI Advocate Join Our Team and Drive
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[...] class=highlight_text>Clinical Research Success At Fortrea, we are committed to accelerating clinical
trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory submissions are completed efficiently. Your expertise will help bring lifechanging treatments to patients faster. In this role, you will be part of [. .. ]
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Job am 04.12.2025 bei Jobleads gefunden
Site Budget Contract Specialist
• München, Bayern
Site Budget Contract
Specialist Fortrea Join to apply for the Site Budget Contract Specialist role at Fortrea. Be among the first 25 applicants. Principal Talent Acquisition Partner DACH at [...]
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[...] Fortrea/ Driving Data-Driven Talent Strategies/ Stakeholder Engagement/ DEI Advocate Join Our Team and Shape the Future of Clinical Research At Fortrea, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget Contract Specialist, you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and [. .. ]
Job am 23.11.2025 bei Jobleads gefunden
• München, Bayern
Regulatory And
Clinical Start Up
Specialist (Biotech) Join to apply for the Regulatory And Clinical Start Up Specialist (Biotech) role at Progressive Direct message the job poster from [...]
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[...] Progressive Regulatory and Start up Associate/ Specialist Responsible for oversight of assigned global clinical trials Review of regulatory submission documents and packages Support study teams as RA representative Preparation of responses to regulatory requests Support of regulatory interactions as applicable Negotiation of Budgets Contract Management Experience Requirements University degree or professional education e. g. Pharmaceutical/ Medical Technical Assistant with a minimum of 1-2 years [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Executive Medical Director Clinical Development Endocrinology, Europe
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] for tardive dyskinesia, chorea associated with Huntingtons disease, classic congenital adrenal hyperplasia, endometriosis and uterine fibroids, as well as a robust pipeline including multiple compounds in mid-to [...]
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[...] late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, [. .. ] opportunities for marketed products. Your Contributions (include, but are not limited to) : Oversight of the clinical development strategy in the endocrinology therapeutic area Oversight of the design of clinical trials across early to late-stage development to ensure they meet regulatory requirements and scientific standards Lead the writing of protocols and major amendments, design of data collection systems, and preparation of clinical study reports, engaging with external experts as needed Collaboration with Clinical Operations to ensure trials are implemented in [. .. ] of data and identification of evidence generation needs Adhere to Neurocrine Europe quality assurance system and compliance with the relevant SOPs Requirements: The appointed candidate will be a physician with specialist experience/ qualifications in endocrinology and/or a proven track record of clinical development in endocrinology products. MD qualified, ideally with specialist medical qualification in Endocrinology and previous experience in patient care At least 8 years experience in early or late stage clinical development in the pharmaceutical industry, ideally including experience [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Overview Join to apply for the Senior Medical Affairs
Specialist-Region West-Mainz, Köln, Düsseldorf (m/w/d) role at Dexcom. Dexcom Corporation (NASDAQ: DXCM) is a pioneer and a global leader in [...]
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[...] continuous glucose monitoring (CGM) . We aim to improve human health by providing accessible information and insights that lead to better health outcomes. Our future is to [. .. ] millions of lives and are ready to change millions more. This position is focused on medical affairs activities in the region, bridging the company with healthcare professionals (HCPs) and supporting clinical strategy, product development and educational activities. Position Summary The Field Medical Science Specialist/ Medical Affairs Specialist acts as the bridge between the company and healthcare professionals (HCPs) , providing in-depth scientific knowledge, practical medical applications and support for our products and research. The FSS is the medical and scientific [. .. ] updates on current research and clinical practices during product launches, customer meetings and training sessions. Clinical Research Support Support the clinical research teams to identify sites and investigators for clinical trials. Data Dissemination and Insights Gather information from KOLs on how they are using our products. Provide feedback to marketing and sales to help develop marketing materials and commercial strategy. Represent the company at scientific conferences, meetings, and advisory boards, communicating data and engaging in scientific discussions. Compliance and Reporting Ensure [. .. ]
Job am 04.11.2025 bei Jobleads gefunden
Data Analytics Manager Data Technology, SCD
• Liestal, Basel- Landschaft
[. .. ] later than 26th of October 2025. For more information about the position please contact Data Technology Manager Fredrik Larsson at. For questions regarding the recruitment process please [...]
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[...] contact People Culture Specialist Katie Pettersson at. At IKEA we believe that were better when were physically together for collaboration dialogues and conversations. We believe in the power of human interactions; the informal chats the energy belonging and creativity generated by people being in the same place. Our approach is that we spend majority [. .. ] IKEA workplace and with flexibility to work from home when relevant. Remote Work: No Employment Type: Full-time Key Skills SQL, Data Collection, GCP, Master Data Management, R, Data Management, Clinical Trials, User Acceptance Testing, Data Warehouse, SAS, Oracle, Data Analysis Skills Experience: years Vacancy: 1 #J-18808-Ljbffr 68370745 [. .. ]
Job am 09.10.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] with post-market solutions, including medical affairs planning and execution of the medical/ scientific engagement strategy. They address and deliver strategic pre-launch and launch medical activities needs for [...]
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[...] patient, clinical, access and value to health care systems. Providing expertise in the development and execution of the overarching strategies and providing inputs during design and along the end-to-end execution of programs. About The Role The Global Medical Affairs (GMA) team acts as enterprise medical voice across the asset lifecycle [. .. ] for promotional and non-promotional global materials; deputise for the Executive Medical Director across PMAT/ GCT/ GPT, regional alignment, internal decision boards and external activities. Essential Requirements: Medical Degree (MD) Specialist Degree or specialist qualification related to Rheumatology. 5+ years in Pharmaceutical Industry with experience in Medical Affairs at global level and/or Clinical Development Firm working knowledge of Clinical Trials, including Good Clinical Practice (GCP, ) scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities Deep understanding of health care systems and key external stakeholders Critical thinker, agile mindset, ability to navigate uncertainty without major supervision, ability to truly collaborate [. .. ]
Job am 28.09.2025 bei Jobleads gefunden
Senior Statistical Programmer (Home-Based, anywhere in Europe)
[. .. ] anywhere in Europe) Hobson Prior is seeking a Senior Statistical Programmer to join our clients team. This is a remote role anywhere within Mainland Europe. This role [...]
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[...] focuses on supporting clinical activities in oncology and rare disease trials. You will be responsible for developing statistical reports and datasets while managing outsourced tasks. You will also lead projects to ensure timely and high-quality results and maintain positive collaborations. Responsibilities: Develop statistical reports and datasets. Manage outsourced data tasks. Lead projects to ensure quality and timeliness. Collaborate effectively with [. .. ] more or applying to this exciting opportunity, please click Apply and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please select Contact me at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. #J-18808-Ljbffr [. .. ]
Job am 26.07.2025 bei Jobleads gefunden
• Berlin
Absolventen, Einsteiger, Trainees
[. .. ] and the US markets Location: (hybrid) Contract type: 1-year fixed term with the possibility of extension to a permanent contract. # # About AMBOSSAMBOSS is a learning [...]
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[...] and clinical decision support tool striving to empower medical professionals across the globe to provide the best possible care. Our founders set out in 2011 to create a tool they would have hoped to have as medical students and doctors. Since then we have grown to currently operate in 180 countries and [. .. ] traction in Germany and the US. Currently, we are pursuing this mission with more than 600+ employees in our offices in Berlin, Cologne, New York, and Cagliari. The Customer Success Specialist plays a key role in ensuring our institutional partners unlock the full value of AMBOSS. By supporting new customer onboarding, solving technical access needs, and addressing institutional users issues, this role helps embed AMBOSS into daily clinical and teaching routines. Strategically, the position strengthens customer satisfaction, retention, and growth. Reporting [. .. ] up on time, coordinating communication strategies and campaigns, and creating clear external instructions that highlight AMBOSSs value and explain how to activate institutional licenses. Drive activation of AMBOSS licenses and trials by executing targeted outreach campaigns, monitoring performance, and evaluating impact through usage data and survey insights. Conduct in-depth analysis of customer adoption patterns, translating data into actionable insights and recommendations that support institutional success and long-term engagement. Partner with the B2B Sales Team to plan and execute migrations [. .. ]
Job vor 5 Tagen bei Neuvoo gefunden
Bristol Myers Squibb
Therapeutic Area Specialist, Cardiovascular (m/w/d) - Cardiomyopathy-Gebiet 10203: Jena, Dresden, Cottbus
• Dresden, Saxony
Abgeschlossenes Studium
[. .. ] chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Beschreibung der Position: Als [...]
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[...] Therapeutic Area Specialist Cardiomyopathy (m/w/d) in dem Gebiet Jena, Dresden, Cottbus bist Du verantwortlich für den Verkauf unseres innovativen kardiologischen Produktes in Kliniken und Praxen. Du entwickelst ein tiefgehendes Verständnis von Stakeholdern und Netzwerken Deiner Accounts und analysierst, welche Wege Patienten in Deiner Region von ersten Symptomen bis zur Diagnose und [. .. ] integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-[. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
Edwards Lifesciences
Senior Clinical Safety Specialist
• Garching, Bavaria
[. .. ] applications of the technology. The Edwards SAPIEN valve platform continues to raise the bar as the most widely studied transcatheter heart valve worldwide. We have an opportunity [...]
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[...] to join our Clinical Safety Team in Munich Germany, on an 18-month contract. As either an experienced Medical Device or Drug Safety Specialist OR a Medical Professional with an active interest in clinical trial safety and cardiology, the successful candidate will be the Clinical Safety contact for European Clinical Trials. This position has responsibility for meeting all reporting and recording requirements of Safety Data (Adverse Events) per current industry regulations. This role is to cover maternity leave on a fixed term contract of 18-months, starting March 2026. The role will be office based in Munich (some hybrid working may [. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
ICON
Clinical Research Associate II/ Senior Clinical Research Associate Large Pharma
• Frankfurt, Hessen
Work-Life-Balance
CRA II/ Senior CRA Large Pharma ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and [...]
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[...] we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies What You Will Be Doing: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to [. .. ]
Job am 07.12.2025 bei Neuvoo gefunden
AMBOSS
Junior Customer Success Manager
• Berlin
Absolventen, Einsteiger, Trainees
Hello, we are AMBOSS and looking for a sparring partner for our customers in the International and the US markets Location: Berlin (hybrid) About AMBOSSAMBOSS is a learning and
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[...] class=highlight_text>clinical decision support tool striving to empower medical professionals across the globe to provide the best possible care. Our founders set out in to create a tool they would have hoped to have as medical students and doctors. Since then we have grown to currently operate in countries and have gained [. .. ] we are pursuing this mission with more than + employees in our offices in Berlin, Cologne, New York, and Cagliari. Why can this position be exciting for you? The Customer Success
Specialist plays a key role in ensuring our institutional partners unlock the full value of AMBOSS. By supporting new customer onboarding, solving technical access needs, and addressing institutional users issues, this role helps embed AMBOSS into daily clinical and teaching routines. Strategically, the position strengthens customer satisfaction, retention, and growth. Reporting [. .. ] up on time, coordinating communication strategies and campaigns, and creating clear external instructions that highlight AMBOSSs value and explain how to activate institutional licenses. Drive activation of AMBOSS licenses and
trials by executing targeted outreach campaigns, monitoring performance, and evaluating impact through usage data and survey insights. Conduct in-depth analysis of customer adoption patterns, translating data into actionable insights and recommendations that support institutional success and long-term engagement. Partner with the B2B Sales Team to plan and execute migrations [. .. ]
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Job am 07.12.2025 bei Neuvoo gefunden
Med Communications International
Pharmacist-Medical Information Specialist (English)
• Berlin
Homeoffice möglich
Work-Life-Balance
Pharmacist/ Medical Information
Specialist-(English Speaker) Pharmacist-Germany (Remote) Must have for this role: Degree: Advanced health professional degree (Pharm D preferred) or relevant, equivalent
clinical experience. Experience: At least [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 3 to 5 years as a Pharmacist Fluent: C1 or C2-English German Speaker Its about: Unlocking Your Potential Transition from the Community Pharmacy to a Rewarding Career as a Medical Information Specialist Introduction: Are you a Pharmacist looking to take the next step in your [. .. ] Stay Updated : Pharmaceuticals and medical treatments are constantly evolving. By joining Med Communications, youll stay at the forefront of the latest advancements. Youll engage with cutting-edge research, clinical trials, and breakthrough therapies. Transferable Skills : Your experience as a Community Pharmacist equips you with valuable skills like patient communication, drug knowledge, and attention to detail. These skills will not only serve you well in your new role but also make the transition smoother. Quality of Life Improvements: Work-Life [. .. ]
Job am 15.09.2025 bei Job-Consult gefunden
Recruiter Vitaly Pryadka
Oncologist, Norway
• Norwegen/ sonstiges/ Europa
[. .. ] in norway expected tasks medical oncological treatment and follow up with cancer patients radiation treatment palliative radiation and curative breast radiation general palliative treatment for most tumour [...]
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[...] types participation in clinical trials and research training and guidance of resident doctors qualifications european authorisation as a medical professional european certification as an oncologist good overall knowledge and expertise in the oncology field communication skills in one of the scandinavian languages free language course will be offered to foreign candidates personal qualities you interact [. .. ] the subject and opportunities for research work exchange and professional development follow up by an advisor before during and after employment if necessary we offer help with norwegian authorisation and specialist approval assistance with accommodation and travel your family will also be taken care of in the process if necessary free language school done through teams skype to apply please send your cv mentioning reference dm at info phd jobs net tel contact person vitaly pryadka web http www phd jobs [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Specialist pro Jahr?
Als Clinical Trials Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 25 offene Stellenanzeigen für Clinical Trials Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Specialist Jobs?
Aktuell suchen 8 Unternehmen nach Bewerbern für Clinical Trials Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Specialist Stellenangebote:
- team2work (1 Job)
- Bristol Myers Squibb (1 Job)
- Edwards Lifesciences (1 Job)
- ICON (1 Job)
- AMBOSS (1 Job)
- Med Communications International (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Specialist Jobs werden derzeit in Bayern (4 Jobs), Berlin (3 Jobs) und Nordrhein-Westfalen (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Specialist Jobs?
Clinical Trials Specialist Jobs gehören zum Berufsfeld Pharmazie.
