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15 Jobs für Clinical Study Coordinator


Stellenangebote Clinical Study Coordinator Jobs


Job gestern bei Jobleads gefunden

Studienkoordinator (m/w/d)

• München, Bayern Betriebliche Altersvorsorge Jobticket Tarifvertrag Join the LMU Klinikum München team as a Study Coordinator (m/w/d) . This role involves coordinating clinical research on adrenal disorders and sex development variants within a multinational research group. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Ihr Aufgabenbereich Vor- und Nachbereitung der Patientenvisiten in der Studienambulanz Mitarbeit an multizentrischen, internationalen klinischen Studien Unterstützung des Studienteams vor Ort bei der Koordination und Durchführung der Studien Betreuung der Patienten während der Studienphase Vorbereitung (inklusive Terminvereinbarung) [. .. ]

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Job vor 4 Tagen bei Jobleads gefunden

Clinical Quality Manager (m/f/d) - Cell Therapy

• Hamburg [. .. ] their potential. With us, every single employee puts patients first. Make an impact in advancing Cell Therapy by ensuring the highest standards of quality and compliance. We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] are seeking a Clinical Quality Manager (CQM) (m/f/d) - Cell Therapy to join our Cell Therapy Clinical Operations (CTCO) team. In this role, you will collaborate with the Business Processes, Quality Learning (BPQL) team to provide expert guidance and coaching, enabling the successful delivery of Cell Therapy studies by the Site Management [. .. ] (VQV) , if applicable. Foster an engaging quality culture within CT SMM; develop and implement compliance improvement initiatives. Provide country-level consultation during RIST, inspections, and audits; act as audit coordinator for internal audits and serve as SME during sponsor and investigator site inspections. Act as a key member throughout the inspection process, including consultation for inspection responses. Analyze quality metrics and trends to improve performance and proactively manage issues. Participate in regional CT SMM leadership teams and facilitate quality review [. .. ] equivalent professional experience. At least 4 years of operational and/or quality experience in drug development within a pharmaceutical or clinical setting. Solid understanding of business processes, technology, and clinical study information systems. Proven time management skills and the ability to deliver timely responses and support to internal and external stakeholders. Experience working successfully and collaboratively with both internal teams and external partners. Excellent written and verbal communication skills, with the ability to influence, negotiate, collaborate, solve problems, present effectively, mentor [. .. ]

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Job vor 8 Tagen bei Jobleads gefunden

Director, Market Access, Health Technology Assessment Ops Hematology (EU)

• Basel, Basel- Stadt Führungs-/ Leitungspositionen [. .. ] most importantly, share our passionate interest in fighting cancer. General Description:We are hiring an experienced EU HTA Coordination Lead to manage all operational activities related to the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] EU HTA Joint Clinical Assessment (JCA) and Joint Scientific Consultation (JSC) processes for assigned products. In this role, you will serve as the cross-functional coordinator responsible for ensuring timely, high-quality execution of all JCA and JSC procedural steps in alignment with the GVAP Portfolio Lead, who retains accountability for JCA strategy, JCA dossier, and JSC briefing book development. You will coordinate global, regional, and country contributors; manage project timelines; ensure consistent evidence inputs; lead [. .. ] regulatory affairs, incl. regulatory scenario planning, final assessment scope received, changes to indication etc. Ensure close collaboration and alignment with HEOR on PICO simulation, SLR, ITC timeline, information retrieval process, study list development. Ensure timely delivery of cross-functional contributions and maintain strong version control and documentation quality. Identify key risks early, propose mitigation strategies, and ensure procedural readiness at all stages. Internal Expertise Building Continuous Improvement Drive continuous improvement by integrating lessons learned and optimizing internal workflows, templates, and operational [. .. ]

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Job vor 9 Tagen bei Jobleads gefunden Director, Market Access, Health Technology Assessment Ops Hematology (EU) • Basel, Basel- Stadt Führungs-/ Leitungspositionen [. .. ] importantly, share our passionate interest in fighting cancer. General Description We are hiring an experienced EU HTA Coordination Lead to manage all operational activities related to the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] EU HTA Joint Clinical Assessment (JCA) and Joint Scientific Consultation (JSC) processes for assigned products. In this role, you will serve as the cross-functional coordinator responsible for ensuring timely, high-quality execution of all JCA and JSC procedural steps in alignment with the GVAP Portfolio Lead, who retains accountability for JCA strategy, JCA dossier, and JSC briefing book development. You will coordinate global, regional, and country contributors; manage project timelines; ensure consistent evidence inputs; lead [. .. ] regulatory affairs, incl. regulatory scenario planning, final assessment scope received, changes to indication etc. Ensure close collaboration and alignment with HEOR on PICO simulation, SLR, ITC timeline, information retrieval process, study list development. Ensure timely delivery of cross-functional contributions and maintain strong version control and documentation quality. Identify key risks early, propose mitigation strategies, and ensure procedural readiness at all stages. Internal Expertise Building Continuous Improvement Drive continuous improvement by integrating lessons learned and optimizing internal workflows, templates, and operational [. .. ]

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Job vor 11 Tagen bei Jobleads gefunden

Clinical Project Coordinator

• München, Bayern Job Summary Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and engage [...]
MEHR INFOS ZUM STELLENANGEBOT[...] in clinical trial management on a daytoday level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the companys success. Responsibilities Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and [. .. ]

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Job am 25.11.2025 bei Jobleads gefunden

Senior Regional Clinical Research Coordinator (Central Eastern Europe)

Senior Regional Clinical Research Coordinator (Central Eastern Europe) Europe Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. The [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Iterative Health Site Network is a premier network of 70+ clinical research sites across US and Europe accelerating the path to market for gastrointestinal (GI) and [. .. ] success and growth of our partner sites by empowering them with tech-enabled services. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Why this role exists Were scaling an ex-US site network across Central Eastern Europe and Georgia. With 20+ active sites and more studies coming, we need a senior coordinator who keeps studies moving across countriesmaking start-[. .. ]

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Job am 21.11.2025 bei Jobleads gefunden Clinical Project Coordinator • München, Bayern Job Summary Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the companys success. Responsibilities Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; [. .. ]

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Job am 15.09.2025 bei Jobleads gefunden

Associate Clinical Trial Manager (PhD) - Infectious Disease/ Immunology

• München, Bayern Job Summary Medpace is currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (a CTM) to join our Clinical Trial [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Management team. The a CTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills [. .. ] expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM) . Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Manage and perform quality control of our [. .. ]

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Job am 11.09.2025 bei Jobleads gefunden

Associate Clinical Trial Manager (PhD) - Neuroscience/ Ophthalmology

• München, Bayern Job Summary Medpace is currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (a CTM) to join our Clinical Trial [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Management team. The a CTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills [. .. ] expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM) . Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Manage and perform quality control of our [. .. ]

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Job vor 3 Tagen bei Neuvoo gefunden IQVIA

Clinical Research Coordinator (m/w/d) Teilzeit in Münster

• Münster, North Rhine- Westphalia Muenster;Kreisfreie Stadt Muenster Teilzeit Sind Sie auf der Suche nach einer Chance oder einer neuen Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht eine/n engagierte/ n Study [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Nurse/ Clinical Research Coordinator (m/w/d) zur Unterstützung einer klinischen Studie am Standort in Münster. Diese Teilzeitstelle (24 Stunden pro Woche) mit Start per sofort ist zunächst bis zum 30.08.20 26 zu besetzen. Zu den täglichen Aufgaben gehören: Koordination und Organisation klinischer Studienabläufe Sicherstellung eines sicheren Studienumfelds gemäß Gesundheits- und Sicherheitsrichtlinien [. .. ]

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Job vor 6 Tagen bei Neuvoo gefunden Astra Zeneca Clinical Quality Manager (m/f/d) - Cell Therapy • Hamburg [. .. ] their potential. With us, every single employee puts patients first. Make an impact in advancing Cell Therapy by ensuring the highest standards of quality and compliance. We [...]
MEHR INFOS ZUM STELLENANGEBOT[...] are seeking a Clinical Quality Manager (CQM) (m/f/d) - Cell Therapy to join our Cell Therapy Clinical Operations (CTCO) team. In this role, you will collaborate with the Business Processes, Quality Learning (BPQL) team to provide expert guidance and coaching, enabling the successful delivery of Cell Therapy studies by the Site Management [. .. ] (VQV) , if applicable. Foster an engaging quality culture within CT SMM; develop and implement compliance improvement initiatives. Provide country-level consultation during RIST, inspections, and audits; act as audit coordinator for internal audits and serve as SME during sponsor and investigator site inspections. Act as a key member throughout the inspection process, including consultation for inspection responses. Analyze quality metrics and trends to improve performance and proactively manage issues. Participate in regional CT SMM leadership teams and facilitate quality review [. .. ] equivalent professional experience. At least 4 years of operational and/or quality experience in drug development within a pharmaceutical or clinical setting. Solid understanding of business processes, technology, and clinical study information systems. Proven time management skills and the ability to deliver timely responses and support to internal and external stakeholders. Experience working successfully and collaboratively with both internal teams and external partners. Excellent written and verbal communication skills, with the ability to influence, negotiate, collaborate, solve problems, present effectively, mentor [. .. ]

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Job am 07.12.2025 bei Neuvoo.com gefunden Rapid Trials Clinical Research Coordinator (Part-time, On-site, Independent Contractor) • Chemnitz POSITION SUMMARY Rapid Trials is hiring an experienced Clinical Research Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. [...]
MEHR INFOS ZUM STELLENANGEBOT[...] This part-time, freelance role is based in Chemnitz, Germany. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, and ensuring compliance with protocol, GDPR, and site SOPs. Location: On-[. .. ] Friday Total Project Hours: 520 Reports To: PI or designee KEY RESPONSIBILITIES Prescreening Recruitment Review patient charts/ EMRs for eligibility Serve as contact for interested participants Educate patients about the study Log patient interest and inform CRC/ PI Patient Referral Engagement Introduce participants to CRC Schedule study procedures (eg, Fibroscan, biopsy, EGD) Send appointment reminders Organize transportationand follow-up Request/ track medical records Share results with referral sources Coordinate with CRC Complete Sponsor or CRO logs Documentation Systems Enter data into [. .. ]

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Job am 30.11.2025 bei Neuvoo gefunden GULP experts united Employee as study coordinator (m/f/d) • Hamburg [. .. ] of being taken on by our business partners Tailored further training opportunities and free language courses A wide range of employee benefits Your tasks Management of the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Teamcenter software for study data and documentation Booking test rooms and scheduling test subjects Procurement and provision of study materials and equipment Carrying out the studies: Application of products to subjects skin according to study requirements Carrying out measurements and other tests to evaluate the skin care products Ensuring compliance with safety and ethical [. .. ] the antiperspirant effect under warm conditions Your profile Completed training or studies in the field of natural sciences, cosmetic sciences or a related field Experience in conducting volunteer studies or clinical trials, ideally in the field of skin care or cosmetics Good knowledge in the use of database software and Microsoft Office applications Willingness to be present during ongoing studies Very good written and spoken German and English skills Careful way of working and attention to detail Team and communication skills [. .. ]

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Job am 29.11.2025 bei Neuvoo gefunden IQVIA Clinical Research Coordinator/ Study Nurse (m/w/d) - Neuwied • Koblenz, Rhineland- Palatinate Sind Sie auf der Suche nach einer neuen Chance oder Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit einen Clinical Research
MEHR INFOS ZUM STELLENANGEBOT[...] class=highlight_text>Coordinator/ Study Nurse (m/w/d) zur Unterstützung der Durchführung einer klinischen Studie an einem Zentrum in Neuwied. Diese Position ist ab sofort zu besetzen, zunächst befristet auf 6 Monate. Der Umfang beträgt 24 Stunden pro Woche. Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den [. .. ]

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Job am 30.10.2025 bei Job-Consult gefunden Herman Medical Staffing GmbH Clinical Nurse Coordinator-Wound Ostomy Care for Saudi Arabia • Saudi Arabia/ sonstiges/ weltweit clinical nurse coordinator wound ostomy care for saudi arabia herman medical staffing gmbh saudi arabia standard of excellence state of the art prestigious leading hospital in the kingdom [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of saudi arabia is urgently looking for western educated trained and experienced clinical nurse coordinator wound ostomy care hospital the hospital is one of the [. .. ] wound and ostomy care wound ostomy care registered nurse with expertise and experience in wound ostomy care bachelor of science in nursing or equivalent nursing degree not less than years study duration from an accredited program specialist training along with post graduate specialist certification in wound ostomy care cwon wocncb wcn wound care nurse cwcn certified wound care nurse or similar equivalent specialist training certification post graduate diploma and or certification in stoma care wound management wcc wound care certification oms [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Clinical Study Coordinator pro Jahr?

Als Clinical Study Coordinator verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Clinical Study Coordinator Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 15 offene Stellenanzeigen für Clinical Study Coordinator Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Coordinator Jobs?

Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Study Coordinator Jobs.


Welche Unternehmen suchen nach Bewerbern für Clinical Study Coordinator Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Study Coordinator Stellenangebote:


  • IQVIA (2 Jobs)
  • Astra Zeneca (1 Job)
  • Rapid Trials (1 Job)
  • GULP experts united (1 Job)
  • Herman Medical Staffing GmbH (1 Job)


In welchen Bundesländern werden die meisten Clinical Study Coordinator Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Study Coordinator Jobs werden derzeit in Bayern (5 Jobs), Hamburg (3 Jobs) und Nordrhein-Westfalen (1 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Study Coordinator Jobs?

Clinical Study Coordinator Jobs gehören zum Berufsfeld Medizintechnik.


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