15 Jobs für Clinical Study Coordinator
Stellenangebote Clinical Study Coordinator Jobs
Job vor 10 Tagen bei Jobleads gefunden
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 Iterative [...]
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[...] 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-[. .. ]
Job am 14.10.2025 bei Jobleads gefunden
• Allschwil, Basel- Landschaft
Führungs-/ Leitungspositionen
[. .. ] Internal job title: Head of Department In their native language, Swiss TPH employees talk about what motivates them in their daily work. Scientific Project Leader Sonia Borrell, [...]
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[...] Scientific Project Leader Study Nurse Main Secretary Coordinator Saskia Strasser, Main Secretary Coordinator Ph D Student Scientific Collaborator Clinical Consultant How to apply: Please submit your application online. CV Motivational letter including names and contact information (email or phone number) of 1 2 references Reference letters and diploma Swiss TPH is committed to fostering an inclusive and diverse workplace that values and respects differences across gender, race, ethnicity, disability, [. .. ]
Job am 15.09.2025 bei Jobleads gefunden
• 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 Management [...]
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[...] 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 [. .. ]
Job am 11.09.2025 bei Jobleads gefunden
• 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 Management [...]
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[...] 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 [. .. ]
Job am 01.07.2025 bei Jobleads gefunden
• München, Bayern
Clinical Trial Site Relationship
Coordinator Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team [...]
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[...] in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities in Germany. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel. If you want an exciting career within a [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Sanofi
• Frankfurt, Hessen
Führungs-/ Leitungspositionen
Clinical Operations
Study Country Lead I (COSCL) - all genders Join the engine of Sanofis mission where deep immunoscience meets bold, AI-powered research. In the Clinical Study Unit, [...]
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[...] youll drive breakthroughs that could turn the impossible into possible for millions. About Sanofi: Were an R D-driven, AI-powered biopharma company committed [. .. ] Experience: Bachelors or Masters degree (or higher) in medicine, pharmacy, biology, biochemistry, or related natural science Mandatory: Clinical Research experience Preferred: Project management experience combined with field monitor or site-coordinator background Solid knowledge of clinical development processes and relevant therapeutic areas Core Competencies: Strong project management skills with proven ability to manage complex timelines Excellent problem-solving and risk-management capabilities in clinical study environments Proficiency in data analytics and digital tools, platforms, and systems Change management skills with adaptability [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Sanofi
Clinical Operations Study Country Lead I-all genders
• Berlin
Führungs-/ Leitungspositionen
Clinical Operations
Study Country Lead I (COSCL) - all genders Join the engine of Sanofis mission where deep immunoscience meets bold, AI-powered research. In the Clinical Study Unit, [...]
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[...] youll drive breakthroughs that could turn the impossible into possible for millions. About Sanofi: Were an R D-driven, AI-powered biopharma company committed [. .. ] Experience: Bachelors or Masters degree (or higher) in medicine, pharmacy, biology, biochemistry, or related natural science Mandatory: Clinical Research experience Preferred: Project management experience combined with field monitor or site-coordinator background Solid knowledge of clinical development processes and relevant therapeutic areas Core Competencies: Strong project management skills with proven ability to manage complex timelines Excellent problem-solving and risk-management capabilities in clinical study environments Proficiency in data analytics and digital tools, platforms, and systems Change management skills with adaptability [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Parexel
• Berlin
When our values align, theres no limit to what we can achieve. Parexel is beginning to search for an experienced Senior
Clinical Trial Administrator to join one of our [...]
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[...] key sponsors in the Clinical Trial Specialist. In this role you will provide technical and administrative support to the clinical study teams responsible for clinical trial execution. Some specifics about this advertised role Support moderately complex clinical study activities in support of the Clinical Trial Manager. Work closely with the clinical trial team to ensure trial activities are conducted according to Good Clinical Practice (GCP) and relevant SOPs. May assist with [. .. ] are a few requirements specific to this advertised role. At least 2 years of experience (3yrs preferred) in clinical studies (Pharmaceutical Industry Experience Preferred) . Previous site monitoring or study coordinator experience is preferred. Working knowledge of Good Clinical Practices (GCP) regulations and Standard Operating Procedures. Understanding of study phases and general knowledge of how they apply to clinical development. Demonstrated ability to work independently and in a team environment. Working knowledge of electronic Systems including Trial Master File, CTMS, etc. [. .. ]
Job gestern bei Neuvoo gefunden
Georgetown University in Qatar
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job [...]
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[...] Overview The Clinical Research Coordinator serves as clinical research coordinator for phase I, II, and III oncology clinical trials conducted in the Clinical Research Management Office (CRMO) of Lombardi Comprehensive Cancer Center. Incumbent duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines for minimal risk studies. Schedule and coordinate study-related procedures and assessments while maintaining protocol integrity and patient safety and in accordance with Good Clinical Practice (GCP) guidelines. Assist with triaging phone calls and proactive [. .. ]
Job vor 5 Tagen bei Neuvoo gefunden
GULP experts united
• 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 [...]
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[...] 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 [. .. ]
Job vor 6 Tagen 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
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[...] 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 [. .. ]
▶ Zur Stellenanzeige
Job vor 11 Tagen bei Neuvoo.com gefunden
R D Partners
Clinical Research Coordinator/ / Aachen, Germany
• Aachen
Join us as a
Clinical Research
Coordinator in Aachen and help shape the future of clinical development-freelance flexibility, hospital-based impact. R D Partners is seeking a Clinical Research [...]
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[...] Coordinator to join a hospital site in Germany, on a freelancing basis. This role offers an exciting opportunity to contribute to clinical development within a CRO environment. [. .. ] work in this location. Responsibilities: Coordinate and manage clinical research activities at the hospital site. Oversee patient travel cost reimbursement processes. Collaborate with the clinical team to ensure compliance with study protocols and regulations. Maintain accurate documentation and records for clinical trials. Key Skills and Requirements: Native German language proficiency. Prior experience in clinical research coordination. Strong organizational and communication skills. Ability to work onsite in Aachen, Germany. For more information, please contact Terrah-Leigh Pietersen. If you are interested in [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Medpace
Study Start-up Specialist
• Munich
Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
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[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] employing more than 5, 000 people across 40+ countries. Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator/ Study Start-up Specialist to join our Clinical Operations team in Munich. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the [. .. ]
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 [...]
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[...] 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 [. .. ]
Job am 20.10.2025 bei Neuvoo.com gefunden
Medpace
Experienced Regulatory Submissions (Study Start Up) Coordinator
• Munich
Medpace Overview Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission [...]
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[...] is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5, 000 people across 40+ countries. Job Summary As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team office-based in Munich, and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators, you [. .. ]
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 9 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:
- Sanofi (2 Jobs)
- Medpace (2 Jobs)
- Parexel (1 Job)
- Georgetown University in Qatar (1 Job)
- GULP experts united (1 Job)
- IQVIA (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 (3 Jobs), Berlin (2 Jobs) und Rheinland-Pfalz (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Coordinator Jobs?
Clinical Study Coordinator Jobs gehören zum Berufsfeld Medizintechnik.
