39 Jobs für Clinical Trial Specialist
Stellenangebote Clinical Trial Specialist Jobs
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
• Berlin, BE
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and delivering high-quality clinical trials across international studies. As part of their continued growth, they are seeking an experienced CRA II to support studies across the DACH region but must be [. .. ] maintain study documentation within required timelines Requirements Previous experience working as a Clinical Research Associate Ability to independently perform on-site monitoring visits Strong understanding of ICH-GCP and clinical trial regulations Experience working within a CRO environment is highly desirable Therapeutic area experience in Respiratory, Kidney/ Renal, or Transplant studies is essential Fluent German and English language skills Willingness and ability to travel regularly across the DACH region Why Apply? Join a global CRO recognised for its specialist expertise and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Leipzig, SN
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and delivering high-quality clinical trials across international studies. As part of their continued growth, they are seeking an experienced CRA II to support studies across the DACH region but must be [. .. ] maintain study documentation within required timelines Requirements Previous experience working as a Clinical Research Associate Ability to independently perform on-site monitoring visits Strong understanding of ICH-GCP and clinical trial regulations Experience working within a CRO environment is highly desirable Therapeutic area experience in Respiratory, Kidney/ Renal, or Transplant studies is essential Fluent German and English language skills Willingness and ability to travel regularly across the DACH region Why Apply? Join a global CRO recognised for its specialist expertise and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Munich, BY
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and delivering high-quality clinical trials across international studies. As part of their continued growth, they are seeking an experienced CRA II to support studies across the DACH region but must be [. .. ] maintain study documentation within required timelines Requirements Previous experience working as a Clinical Research Associate Ability to independently perform on-site monitoring visits Strong understanding of ICH-GCP and clinical trial regulations Experience working within a CRO environment is highly desirable Therapeutic area experience in Respiratory, Kidney/ Renal, or Transplant studies is essential Fluent German and English language skills Willingness and ability to travel regularly across the DACH region Why Apply? Join a global CRO recognised for its specialist expertise and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Dortmund, NW
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and delivering high-quality clinical trials across international studies. As part of their continued growth, they are seeking an experienced CRA II to support studies across the DACH region but must be [. .. ] maintain study documentation within required timelines Requirements Previous experience working as a Clinical Research Associate Ability to independently perform on-site monitoring visits Strong understanding of ICH-GCP and clinical trial regulations Experience working within a CRO environment is highly desirable Therapeutic area experience in Respiratory, Kidney/ Renal, or Transplant studies is essential Fluent German and English language skills Willingness and ability to travel regularly across the DACH region Why Apply? Join a global CRO recognised for its specialist expertise and [. .. ]
Job am 06.09.2026 bei Mindmatch.ai gefunden
RBW Consulting
Clinical Research Associate II
• Hamburg, HH
Clinical Research Associate II (CRA II) Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in complex and specialist therapeutic areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and delivering high-quality clinical trials across international studies. As part of their continued growth, they are seeking an experienced CRA II to support studies across the DACH region but must be [. .. ] maintain study documentation within required timelines Requirements Previous experience working as a Clinical Research Associate Ability to independently perform on-site monitoring visits Strong understanding of ICH-GCP and clinical trial regulations Experience working within a CRO environment is highly desirable Therapeutic area experience in Respiratory, Kidney/ Renal, or Transplant studies is essential Fluent German and English language skills Willingness and ability to travel regularly across the DACH region Why Apply? Join a global CRO recognised for its specialist expertise and [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
BD
Field Clinical Specialist Switzerland
• AT- 2 Lavamünd
Job Description As a Field
Clinical Specialist in the Advanced Patient Monitoring division, you will be responsible for providing clinical expertise and support for our highly innovative technologies in Hemodynamic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Monitoring in hospitals across Switzerland. Your role will involve educating and training healthcare professionals on the use of medical devices, including during surgical procedures and in the [. .. ] procedures in the operating room and patient care in the intensive care unit. Deliver product demonstrations, clinical training, and education programs for healthcare professionals. Support product launches, implementations, evaluations, and trial placements in hospitals and healthcare institutions. Partner closely with the Sales team to identify and develop business opportunities through clinical expertise and value-based discussions. Participate in customer meetings, workshops, presentations, scientific congresses, and industry events. Develop and implement customer-specific clinical solutions and monitoring concepts that improve patient care [. .. ]
Neu Job vor 2 Std. bei Mindmatch.ai gefunden
Novartis
• AT- 2 Lavamünd
Novartis in Austria is seeking a
Clinical Scientific Expert I to support global clinical
trial activities, focusing on data review, safety signals and data integrity. The role contributes [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to data review plans, CRF development, and cross-functional collaboration to ensure high-quality study outcomes in compliance with ICH-GCP and regulatory requirements. Strong scientific background and experience with data systems (EDC, Excel) are valued as [. .. ]
Job vor 4 Tagen bei Mindmatch.ai gefunden
Rivia
Senior Infrastructure Engineer
• AT- 2 Lavamünd
About Rivia Rivia is a technology company building a data engine that powers the future of
clinical trial intelligence. Rivia was founded on the belief that new drugs can be [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] brought to market more successfully with a fraction of todays capital. Biotechs are the source of most therapeutic innovation, yet clinical development is constantly constrained by fragmented data and outdated tooling. Rivia unifies clinical trial data at scale [. .. ] Actions or equivalent) . An AInative way of working: you use agents (Claude Code or similar) for real infrastructure work and can show concrete examples. Comfortable being the only infrastructure specialist on the team: selfdirected, you find and fix problems without being asked. Bonus Keycloak or similar identity provider operations (OIDC, SSO, secrets management) . Spark or largescale data pipeline infrastructure experience. Exposure to regulated environments (ISO 27001, audit support) . Datadog or a comparable observability stack. Our Values At Rivia, [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
Planet Pharma
• AT- 2 Lavamünd
Führungs-/ Leitungspositionen
We are seeking an experienced and highly motivated Associate Director,
Clinical Biomarker Biostatistics to play a pivotal role in advancing our clinical development and precision medicine strategies. This is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an exciting opportunity for a strategic and handson biostatistician to drive the statistical leadership of biomarker initiatives across a diverse clinical portfolio. As a key member of the Biometrics organization, you will [. .. ] pharmaceutical, biotechnology, or healthcare research environments. Extensive experience supporting biomarker development within clinical drug development programs. Deep understanding of statistical methodologies for biomarker research and precision medicine. Expertise in clinical trial design and analysis. Strong knowledge of regulatory expectations related to biomarker and companion diagnostic development. Advanced proficiency in statistical programming and analysis tools such as R and/or SAS. Demonstrated ability to influence crossfunctional teams and senior stakeholders. Excellent communication and scientific presentation skills. Preferred Qualifications Experience supporting immunology, rare [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Job vor 5 Tagen bei Mindmatch.ai gefunden
MSD
Specialist Upstream Operations (m/f/d)
• AT- 2 Lavamünd
[. .. ] they belong at Schachen, but that the site belongs to and is shaped by them. Our Schachen Biotech is a premier, stateoftheart facility that integrates advanced technologies [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] into the earlystage clinical pipeline, refining them for future commercial launch. The site supports biologics drug substance manufacturing for earlyphase clinical supply and serves as a hub for technology innovation and strategic advancement. The Specialist Upstream Operations position requires fulltime physical presence at the site to support manufacturing and to enable optimal integration into an existing team. As a member of the growing manufacturing team at our company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of earlyphase [. .. ] to our employees and the community around us. Our Werthenstein Bio Pharma site in Schachen is where we conduct cuttingedge research, develop and analyze new biological agents and supply clinical trial products for global clinical studies. The site is also home to one of our global forensic laboratories where we carefully monitor our products through the supply chain to ensure security and safety for our patients. Required Skills Accountability Accountability Adaptability Business Agility Competency Management Contract Manufacturing Data Analysis Deviation Management [. .. ]
Job vor 11 Tagen bei Mindmatch.ai gefunden
Gouya Insights
• AT- 9 Wien
Looking for an opportunity to put your
clinical project management skills to the test? We are seeking an experienced Clinical Project Manager to join our team at Gouya Insights [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Gmb H Co KG, a clinical development consulting and clinical research services company supporting innovative biotech, pharmaceutical, and medical device companies. As Clinical Project Manager, you will take operational ownership of early-phase clinical studies and development projects, working at the interface between our clients, clinical sites, CROs, specialist vendors, and internal clinical development experts. You will translate clinical development strategies into operational execution, coordinate cross-functional project teams, and ensure timely delivery of projects within budget constraints, maintaining high quality and GCP standards. This role suits a proactive leader who enjoys taking ownership, working in a dynamic early-development environment, and solving the operational challenges that arise when multiple partners need to work together. Key Responsibilities Clinical Trial Management Lead the operational delivery of assigned clinical studies from planning and start-up through study execution, database lock, and close-out. Develop and manage study plans, timelines, budgets, deliverables, and risk-mitigation activities. Lead regulatory activities to ensure timely approvals and keep site activation on schedule. Coordinate site feasibility, [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
Verbatim Pharma
Business Development Manager
• AT- 2 Lavamünd
Business Development Manager Pharma Logistics Industry: Pharmaceutical Life Sciences Logistics The Opportunity We are partnering with a leading global
specialist in pharmaceutical and healthcare logistics to recruit an experienced [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Business Development Manager to support the continued growth of its Swiss business. This is a commercially focused role responsible for developing new business across the pharmaceutical and life sciences market, working with organisations requiring complex, time-critical and temperature-sensitive logistics [. .. ] across the Swiss market. Identify, target and win new customers across pharmaceutical, biotechnology and wider life sciences organisations. Develop opportunities with other relevant healthcare customers, including hospitals, central laboratories and clinical research organisations. Build relationships with key decision-makers across supply chain, logistics, procurement, clinical operations and associated functions. Sell specialist logistics solutions including temperature-controlled, time-critical and regulated transportation and distribution services. Manage the full sales cycle from initial prospecting and qualification through to proposal, negotiation and contract award. [. .. ] autonomously and manage a national territory. Willingness to travel regularly for customer meetings across Switzerland. The Ideal Profile We are particularly interested in individuals currently working within pharma logistics, clinical trial logistics, healthcare transportation, cold chain, specialist courier or life sciences supply chain services. This opportunity would suit a commercially driven individual who enjoys hunting for new business, developing long-term customer relationships and working within a highly specialised and regulated market. Why Apply? This is an opportunity to join an [. .. ]
Neu Job vor 2 Std. bei Jobleads gefunden
• Zürich Zuerich
Führungs-/ Leitungspositionen
[. .. ] top-class education. Put your talent and skills to work with us. Find out more about UZH as an employer Your responsibilities Planning, coordinating and conducting academic and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] industry-sponsored clinical trials from feasibility assessment and study set-up through completion and reporting. Serving as the primary contact for researchers, sponsors, industry partners and other external clients, while building and maintaining collaborative partnerships. Assessing study feasibility, timelines, resources and budgets, and supporting proposal development. Coordinating clinics, nursing staff, laboratories, administrative units [. .. ] complete and audit-ready documentation. Establishing and continuously improving study processes, SOPs and quality systems, including the management of monitoring visits, audits, inspections, deviations and corrective actions. Managing the clinical trial portfolio, monitoring milestones and resources, and reporting progress to management and governance bodies. Recruiting, supervising and supporting the development of a veterinary nurse dedicated to clinical trial activities. Contributing to the strategic development and expansion of clinical trial services. Your profile We are seeking a veterinarian with a strong interest in clinical research and experience managing complex projects and collaborations. The ideal candidate will have: A degree in veterinary medicine; a doctorate or specialist qualification is an advantage. Several years of clinical veterinary experience, ideally combined with experience planning, managing or conducting clinical trials. Knowledge of clinical research standards and requirements (e. g. GCP/ VICH GCP, Gx P, ethics, study documentation and audit readiness) or a willingness to develop expertise in these areas. Experience working [. .. ]
Job gestern bei Jobleads gefunden
Senior Clinical Data Scientist (m/f/d)
• Frankfurt, Hesse
[. .. ] countries are dedicated to this mission. Would you like to become part of our success story? Join Merz Aesthetics The following responsibilities are awaiting you: You develop, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] execute, and optimize clinical data strategies across the development lifecycle by leveraging advanced analytics, risk-based methodologies, and emerging technologies. You apply automated and AI-enabled approaches to clinical data review to identify data inconsistencies, protocol deviations, and emerging risks. You develop and standardize dashboards, study metrics, and data visualizations to support effective clinical trial oversight and data-driven decision-making. You support risk-based quality management activities by monitoring critical-to-quality data points, quality tolerance limits, and key risk indicators. You oversee the integration and exchange of data from multiple clinical systems and external sources, ensuring consistency, quality, and traceability across the data [. .. ] training : Your personal and professional development is the key to success for us. To foster this, we conduct regular development discussions and facilitate a wide range of management and specialist training courses, soft skills courses, e-learning courses, language courses and coaching sessions. Find out more about our benefits at https:/ / careers. merz-aesthetics. com. We look forward to your application #J-18808-Ljbffr 03688780 [. .. ]
Job gestern bei Jobleads gefunden
Director Clinical Trial Operations
• Zürich Zuerich
Führungs-/ Leitungspositionen
Director
Clinical Trial Operations Founded in 2025 at the University of Zurich, the Zurich Hub for Drug and Device Development (ZH3D) supports the development of medicinal products and medical devices [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] through regulatory expertise, quality assurance and specialised Gx P services. For the University Animal Hospital Zurich, we are seeking a highly organised veterinarian to [. .. ] seeking a veterinarian with a strong interest in clinical research and experience managing complex projects and collaborations. The ideal candidate will have: A degree in veterinary medicine; a doctorate or specialist qualification is an advantage. Several years of clinical veterinary experience, ideally combined with experience planning, managing or conducting clinical trials. Knowledge of clinical research standards and requirements (e. g. GCP/ VICH GCP, Gx P, ethics, study documentation and audit readiness) or a willingness to develop expertise in these areas. Experience working [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Regulatory Affairs Manager EU (m/f/d)
• Frankfurt, Hesse
[. .. ] part of our success story? Join Merz Aesthetics This role is limited to 18 months. The following responsibilities are awaiting you: You prepare and submit applications for [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] conformity assessments and clinical trials involving non-active implantable class III medical devices in the EU. You coordinate timely and accurate responses to questions from Notified Bodies and Competent Authorities. You compile, assess, and update CE technical documentation and clinical trial application dossiers, including documentation provided by third parties. You advise cross-functional development teams on quality, analytical, preclinical, and clinical requirements to support the acceptance of regulatory submissions. You prepare and maintain product information in accordance with company core data, applicable legislation, and relevant guidelines. You manage the regulatory life [. .. ] Ongoing training: Your personal and professional development is the key to success for us. To foster this, we conduct regular development discussions and facilitate a wide range of management and specialist training courses, soft skills courses, e-learning courses, language courses and coaching sessions. Find out more about our benefits at https:/ / careers. merz-aesthetics. com. We look forward to your application #J-18808-Ljbffr 03442162 [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
Associate Director Biostatistics
• Lavamünd, Kärnten Lavamuend
Führungs-/ Leitungspositionen
We are seeking an experienced and highly motivated Associate Director,
Clinical Biomarker Biostatistics to play a pivotal role in advancing our clinical development and precision medicine strategies. This is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an exciting opportunity for a strategic and handson biostatistician to drive the statistical leadership of biomarker initiatives across a diverse clinical portfolio. As a key member of the Biometrics organization, you will [. .. ] pharmaceutical, biotechnology, or healthcare research environments. Extensive experience supporting biomarker development within clinical drug development programs. Deep understanding of statistical methodologies for biomarker research and precision medicine. Expertise in clinical trial design and analysis. Strong knowledge of regulatory expectations related to biomarker and companion diagnostic development. Advanced proficiency in statistical programming and analysis tools such as R and/or SAS. Demonstrated ability to influence crossfunctional teams and senior stakeholders. Excellent communication and scientific presentation skills. Preferred Qualifications Experience supporting immunology, rare [. .. ] that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent/ direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We [. .. ]
Job vor 9 Tagen bei Jobleads gefunden
Clinical Configuration Specialist I
Join the Centricity Research Team Centricity Research is one of North Americas largest
clinical research networks and a fully centralized Integrated Research Organization (IRO) . We conduct Phase I-IV [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical trials across more than 35 therapeutic areas, partnering with leading pharmaceutical, biotechnology, and medical device companies to advance healthcare through innovative clinical research. Join our growing team and build a rewarding career while helping bring new treatments to patients. About the Role We are seeking a Clinical Configuration Specialist I to support the design, configuration, and ongoing maintenance of study-specific electronic source documents and CTMS workflows. This role plays a critical part in ensuring study teams and site users have accurate, intuitive tools to support data collection, study execution, and financial tracking. Youll collaborate closely with cross-functional [. .. ] within the CTMS in alignment with study protocols and Centricity standards Build and maintain CTMS visit templates and financial configurations to ensure accurate task tracking and billing Review executed Clinical Trial Agreements (CTAs) to determine appropriate visit structures and associated budgets Enter additional invoiceable CTA items into the CTMS to support accurate sponsor and CRO billing Ensure visit schedules and billing items are correctly configured for both clinical and finance teams Maintain working knowledge of study protocols and amendments as they [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
• Sankt Gallen
Job Title: Senior
Specialist, Regulatory Affairs (EU/ Ro W) Job Type: Full time, Permanent Position CPL Life Sciences is collaborating with a growing biotechnology company focused on advancing innovative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies for patients with unmet medical needs. We are seeking an experienced Senior Specialist, Regulatory Affairs (EU/ Ro W) to support global regulatory activities across development and [. .. ] dynamic and collaborative biotech environment. Key Responsibilities Support regulatory leads in the preparation, submission, and maintenance of regulatory applications across EU and Rest of World territories. Coordinate and contribute to Clinical Trial Applications (CTAs) , CTA amendments, pre-and post-authorisation submissions, and annual reports. Assist in the preparation, review, and submission of responses to questions from regulatory authorities. Participate in late stage development activities including initial and new MAAs and potentially any new indications. Ensure all regulatory submissions are complete, compliant, [. .. ]
Job am 08.09.2026 bei Jobleads gefunden
Clinical Research Associate (all levels) - Germany
Homeoffice möglich
Jobticket Work-Life-Balance
EPIC. Evestia
Clinical is a biotech-focused global CRO delivering authentic expertise and personalized support where client need it most. We are building something EPIC. Evestia Clinical is a biotech-focused [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global CRO delivering authentic expertise and personalized support where client need it most. Our foundation is built on four core principles: Innovation [. .. ] to provide expert knowledge and guidance through complex clinical trials in rare disease, oncology, neurology, immunology, and inflammation. At Evestia Clinical, you will become a vital part of a global specialist CRO. This means you will deliver life changing impact through clinical excellence. We are committed to creating development opportunities that allow your skills to grow right alongside ours. If you are inspired by this collaborative environment and ready to change the lives of patients worldwide, wed love to welcome you to our team. About The Role We are looking for a Clinical Research Associate (CRA of all levels) to be responsible for ensuring that the rights and safety of clinical trial participants are protected and that the clinical data obtained are accurate, complete, and verifiable according to source. What will your job look like? Performing all and any visit types while ensuring regulatory and protocol compliance Participate in all aspects of a clinical trial from development and planning to study closure [. .. ]
Job am 06.09.2026 bei Jobleads gefunden
Clinical Research Associate II
Location: Germany Based, Covering DACH Region Join a Global CRO Making a Difference Our client is a highly respected global CRO with deep expertise in complex and
specialist therapeutic [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] areas. Consistently outperforming the wider market, they have built an excellent reputation for scientific expertise, operational excellence, and delivering high-quality clinical trials across international studies. As part of their continued growth, they are seeking an experienced CRA II to support studies across the DACH region but must be based in Germany. The Opportunity This role offers the chance to join a collaborative and well-established clinical operations team, working on innovative [. .. ] maintain study documentation within required timelines Requirements Previous experience working as a Clinical Research Associate Ability to independently perform on-site monitoring visits Strong understanding of ICH-GCP and clinical trial regulations Experience working within a CRO environment is highly desirable Therapeutic area experience in Respiratory, Kidney/ Renal, or Transplant studies is essential Fluent German and English language skills Willingness and ability to travel regularly across the DACH region Why Apply? Join a global CRO recognised for its specialist expertise and [. .. ]
Job am 04.09.2026 bei Jobleads gefunden
Data Transparency Specialist Data Sharing, Anonymisation and Clinical Trial Disclosure (f/m/d-part/ full-time)
• München, Bayern
Your responsibilities will include Assessing data sharing requests, reviewing informed consent forms for data sharing feasibility Redaction of
clinical trial documents and anonymisation of individual patient data Preparing Redaction Proposal [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Document Packages (RPDP) for submission to EMA and Health Canada in compliance with EMA Policy 0070 and Health Canada PRCI Disclosure of clinical trial information for drugs and medical devices: Registering protocols and preparing results for submission to local and [. .. ]
Job am 03.09.2026 bei Jobleads gefunden
Device Support Specialist New Indications Germany-Thüringen area (w/M)
Field Based/Full Time/ 1 year fixed term contract WHAT YOULL DO The Device Support
Specialist, New Indications is a key position within the Center of Excellence business unit, with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a clinical trial patient focus. The primary role of this position is to support clinical trial oncology patients utilizing Tumor Treating Fields (TT Fields) therapy in Germany. This is an exempt, full-time, fieldbased position reporting to the Snr, New Indications DSS Lead, EMEA. Continue to honor our Patient Forward mission Manage administrative [. .. ]
Job am 02.09.2026 bei Jobleads gefunden
Clinical Specialist
• Mannheim, Baden- Württemberg
Accompanying applications (
trial order of measurement parameters and products) in the field of non-invasive patient monitoring at the customers site Development and implementation of individual overall solutions for the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] customer together with the sales staff and subsequent continued support Training of clinical and nursing staff in the companys own training center or in hospitals Product presentation in workshops, at trade fairs and congresses Documentation and forwarding of customer feedback in the CRM system Collaboration with national and international teams such as Customer Service, Marketing and Technical Service Traveling in the assigned region [. .. ]
Job am 30.08.2026 bei Jobleads gefunden
Clinical Specialist, 6-month FTC
• Hamburg
Region to cover: Hamburg Northern Lower Saxony Duties and Responsibilities Accompanying applications (
trial order of measurement parameters and products) in the field of non-invasive patient monitoring at the customers [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] site Development and implementation of individual overall solutions for the customer together with the sales staff and subsequent continued support Training of clinical and nursing staff in the companys own training center or in hospitals Product presentation in workshops, at trade fairs and congresses Documentation and forwarding of customer feedback in the CRM system Collaboration with national and international teams such as Customer Service, Marketing and Technical Service Traveling in the assigned region [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Specialist pro Jahr?
Als Clinical Trial Specialist verdient man zwischen EUR 50.000,- bis EUR 80.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Specialist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 39 offene Stellenanzeigen für Clinical Trial Specialist Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Jobs?
Aktuell suchen 12 Unternehmen nach Bewerbern für Clinical Trial Specialist Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Specialist Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Specialist Stellenangebote:
- RBW Consulting (5 Jobs)
- Planet Pharma (2 Jobs)
- BD (1 Job)
- Novartis (1 Job)
- Rivia (1 Job)
- MSD (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Specialist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Specialist Jobs werden derzeit in Baden-Württemberg (5 Jobs), Hamburg (3 Jobs) und Thüringen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Specialist Jobs?
Clinical Trial Specialist Jobs gehören zum Berufsfeld Medizinisch-technische Assistenz / MTA.
