19 Jobs für Clinical Trials Coordinator
Stellenangebote Clinical Trials Coordinator Jobs
Job vor 7 Tagen bei Mindmatch.ai gefunden
Milestone One
• AT- 9 Wien
A global site enabling services organization in Austria seeks a Site
Coordinator to support
clinical trial activities. Responsibilities include communication between sponsors and sites, patient enrollment tracking, and data management. [...]
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[...] The ideal candidate holds a relevant university degree and has at least 2 years of experience as a site coordinator. Fluent English and the local language are required. This position offers the opportunity to grow [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
PSI CRO
• AT- 9 Wien
Führungs-/ Leitungspositionen
A global
clinical study facilitator is seeking a Site
Coordinator in Vienna to support clinical trial activities. The role involves communication with Sponsors, tracking patient enrollment, and participating in audits. [...]
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[...] Candidates should have a university degree in Life Science and at least 2 years of experience as a site coordinator. Fluent English and local language proficiency are required. Join a [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Zug
Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites in [...]
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[...] stronger study delivery. Please submit CV in English. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICHGCP, protocol requirements within studyspecific defined timelines and enrollment goals. Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility questions are provided in due time. Assist in scheduling and preparation for [. .. ] Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 years of on-the-job experience in a clinical trial environment, where relevant experience has been gained in clinical trials, clinical terminology, and medical research working in the role of a Study Coordinator or similar function. Upperintermediate level of English, with the ability to work in a global team environment. Experience in Oncology, Renal, or Cardiology clinical studies is a plus. Ability to work in a fastpaced environment, with short [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Zug
A global
clinical services firm is seeking a Site
Coordinator to support trial sites in ensuring effective communication with sponsors and CROs. The ideal candidate will have a degree in [...]
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[...] Life Sciences and a minimum of 2 years in a clinical trial environment. Responsibilities include managing patient enrollment, preparing for audits, and tracking data entry. The position offers opportunities for [. .. ]
Job am 06.03.2026 bei Jobleads gefunden
• Wiesbaden, Hessen
Overview Velocity
Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity, we align our [...]
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[...] values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step. Job Summary The Manager, Site Operations is responsible for managing the clinical operations staff, training and onboarding of new staff, managing quality and compliance of clinical work closely with and in support of the Site Director. Able to perform coordinator as well as supervisor duties and fill in during the absence of site coordinators. Able to function as lead coordinator on select protocols. Must be able to work independently and with all staff and customer levels. Responsibilities Work with the Site Director to meet/ exceed the sites financial, operational and [. .. ]
Job am 21.02.2026 bei Jobleads gefunden
• Steinhausen, Zug
[. .. ] our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers. bms. com/working-with-us. Position summary The Business Unit [...]
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[...] Coordinator CHAT Innovative Medicines is an enabler for the Business Unit, going beyond traditional administrative support. The role supports commercial excellence with the BU team and encourages innovative thinking. This role partners closely with the BU Head, BU Team and cross-functional network to optimize operations, facilitate innovation, and ensure the [. .. ] 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 am 17.02.2026 bei Jobleads gefunden
• Eysins, Waadt
Führungs-/ Leitungspositionen
[. .. ] flexible working culture, presenting great opportunities for personal development and career advancement across the globe. We are looking for a highly skilled and strategic Project Manager to [...]
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[...] join our Global Clinical Operations team and lead the delivery of complex global clinical trials. In this role, you will provide leadership and strategic direction to optimize site performance at the global study level, overseeing site and vendor performance while ensuring proactive risk mitigation. You will play a critical role in modernizing the clinical trials under your responsibility by driving innovative, value-adding solutions and [. .. ] quality/ costs) and work with CSLs, CTLs, Data Managers, Clinical Lead (s) and other relevant business partners to implement action plans to resolve and/or mitigate. Participate in Investigator/ Study Coordinator Meetings and promote information sharing with the CSLs as needed. Travel: Position may require domestic/ international travel up to 20 of time. Who you are Minimum Requirements Bachelors Degree Medical or Life Sciences degree in a clinical research related discipline 8-10 years professional and project management experience in delivering [. .. ]
Job am 14.02.2026 bei Jobleads gefunden
Associate Director, Trial Clinical Delivery Lead (all genders)
• Eysins, Waadt
Führungs-/ Leitungspositionen
[. .. ] flexible working culture, presenting great opportunities for personal development and career advancement across the globe. We are looking for a highly skilled and strategic Project Manager to [...]
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[...] join our Global Clinical Operations team and lead the delivery of complex global clinical trials. In this role, you will provide leadership and strategic direction to optimize site performance at the global study level, overseeing site and vendor performance while ensuring proactive risk mitigation. You will play a critical role in modernizing the clinical trials under your responsibility by driving innovative, valueadding solutions and ensuring [. .. ] quality/ costs) and work with CSLs, CTLs, Data Managers, Clinical Lead (s) and other relevant business partners to implement action plans to resolve and/or mitigate. Participate in Investigator/ Study Coordinator Meetings and promote information sharing with the CSLs as needed. Travel: Position may require domestic/ international travel up to 20 of time. Minimum Requirements Bachelors Degree Medical or Life Sciences degree in a clinical research related discipline 8-10 years professional and project management experience in delivering Clinical Operations of [. .. ]
Job am 31.01.2026 bei Jobleads gefunden
• Stein, Baden- Württemberg
[. .. ] too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We [...]
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[...] are hiring a Clinical Research Associate III (m/f/d) Location: EMEA (Flexible) . Your Strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials on human subjects (e. g. , ISO 14155, GCP, MDR, EU, FDA) Ability to manage 1015 study sites independently, from start-up to closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRA IIIs are expected to guide junior team members Handson experience [. .. ] safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our Strength A purpose-driven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure [. .. ]
Job vor 3 Tagen bei Neuvoo.com gefunden
Green Life Science
Job Title:
Clinical Research
Coordinator (CRC) Location: Fully Remote Germany Employment Type: Full-time, Permanent Language Requirement: Native or Fluent German About the Company Our client is a leading [...]
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[...] next-generation, full-service Contract Research Organization (CRO) transforming how clinical trials are delivered. The company combines a world-class clinical operations team with advanced AI-powered software to run faster, more reliable clinical studies for life sciences organizations. By integrating innovative technology with deep clinical expertise, they manage the end-to-end delivery of clinical trials, including study design, patient recruitment, [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
Georgetown University in Qatar
Clinical Research Nurse
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] 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 Serves as Clinical Research Nurse 1 for the Cellular Therapy Program oncology clinical trials conducted in the Lombardi Clinical Trials Office of the Lombardi Comprehensive Cancer Center at Georgetown University. Additional duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Collaborate with investigators and more senior study team members by participating in recruitment and [. .. ] trials. Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials with Clinical Research Coordinators. Collaborate with Data Coordinator (s) to assure the documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. Document and report serious adverse events per protocol and institutional policy. Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Act [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Reesi
Manager:in Studienzentren Netzwerke
• Hamburg
Flexible Arbeitszeiten
[. .. ] strukturiertes Follow-up mit bestehenden Partnern nach Veranstaltungen Qualifikation Pflichtanforderungen Erfahrung im Umfeld klinischer Studien Du hast Erfahrung in der Arbeit mit klinischen Studien z. B. als Study [...]
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[...] Nurse, Study Coordinator, in einem Studienzentrum, einer CRO oder in der Zusammenarbeit mit Studienstandorten. Du verstehst die Abläufe rund um Patientenrekrutierung und Studienkoordination. Erfahrung in der Zusammenarbeit mit medizinischem Fachpersonal Du arbeitest sicher und professionell mit Ärzt:innen, Study Nurses und Studienkoordinator:innen zusammen. Du verstehst ihre Arbeitsrealität und kannst auf Augenhöhe kommunizieren. Freude an [. .. ] Umfeld: Arbeiten in einem motivierten und interdisziplinären Team mit kurzen Entscheidungswegen Weiterentwicklung: Individuelle Förderung und Entwicklungsmöglichkeiten Transparenz: Offene Kommunikationskultur und flache Hierarchien Every year, many cancer patients never learn about clinical trials that could help them not because the trials dont exist, but because the information is fragmented, inconsistent, and difficult to search. This challenge delays over 80 of clinical trials and prevents more than 30 of eligible patients from accessing potentially life-saving treatments. Reesi is a web-based AI platform [. .. ]
Job vor 13 Tagen bei Neuvoo gefunden
IQVIA
Experienced Clinical Trial Coordinator (m/w/d) , Home Office within the Ulm area
• Frankfurt, Hessen
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical
trials. Joining the team provides the opportunity to [...]
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[...] work with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region. You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery. We currently offer an exciting opportunity to join the team as Experienced Clinical Trial Coordinator (m/w/d) to work in home-office within the Ulm/Biberach an der Riß area (e. g. Ulm, Neu-Ulm, Memmingen, Ehingen an der Donau, Ravensburg, Leutkirch im Allgäu, etc. ) . Your responsibilities might include: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with [. .. ]
Job am 06.03.2026 bei Neuvoo gefunden
IQVIA
Senior Clinical Operations Lead-Sponsor Dedicated (m/w/d)
• Berlin
The Senior
Clinical Operations Lead will be responsible to support the Clinical Trial Manager/ operational team in execution of the trial (s) . The function could include direct liaison [...]
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[...] with CROs and other ancillary vendors, as appropriate, to manage relevant trial (s) operational tasks. Maintain effective communication with project team through oral and [. .. ] monitoring organization. Assist in the development and management of study timelines and priorities, including recruitment tools/ strategy and patient retentions plan. Plan and organize meetings with team support (eg. investigator/ coordinator meetings, DMC, SMC, safety call, etc. ) . Assist in the development of the IP and co-medication strategy (Quantities, labels, depots, tracking, etc. ) working closely with other departments. Participate in data review and discrepancy resolution. Participate in coordinating efforts with internal Pharmacovigilance, and safety group. Monitor study-specific [. .. ] other relevant regulatory/ health authority experience. Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously. Prior experience in assisting the conduct and management of multinational clinical trials is preferred. Please note This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to [. .. ]
Job am 19.02.2026 bei Neuvoo gefunden
Massive Bio, Inc.
Patient Relations Coordinator Germany
About Massive Bio Every cancer patient deserves access to treatment options. Massive Bio is an AI-powered precision medicine platform transforming how cancer patients discover and access
clinical trials by eliminating [...]
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[...] the barriers of geography, financial constraints, and information asymmetry that have historically limited enrollment. Founded in 2015 and headquartered in US, Massive Bio is scaling its impact globally by powering operations across multiple countries and bringing innovative cancer treatment options to a rapidly growing and diverse population of [. .. ] leading pharmaceutical companies, contract research organizations (CROs) , and healthcare systems to accelerate drug development and expand equitable access to cutting-edge therapies. About the Role As the Patient Relations Coordinator, you will support cancer patients and caregivers in Germany through structured, compliant communication and coordination. You ll manage patient onboarding, documentation, and follow-ups in our systems while protecting sensitive data under GDPR standards. This role will be engaged as an independent contractor in Germany (self-employed) . Key Responsibilities [. .. ]
Job am 15.02.2026 bei Neuvoo gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d)
• Karlsruhe, Baden- Württemberg
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
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[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ]
Job am 06.02.2026 bei Neuvoo gefunden
Georgetown University in Qatar
Research Data Coordinator I
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] 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 Overview [...]
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[...] The Research Data Coordinator I position is responsible for data management for phase I, II, and III oncology clinical trials conducted within the Clinical Research Management Office (CRMO) of the Lombardi Comprehensive Cancer Center (LCCC) . Additional duties include, but are not limited to: Supports all aspects of clinical research data management for clinical trials conducted in the LCCC Clinical Research Management Office (CRMO) , including collection of data from [. .. ]
Job am 23.01.2026 bei Neuvoo gefunden
Georgetown University in Qatar
Clinical Research Nurse II
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] 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 Serves as Clinical Research Nurse 2 for the Cellular Therapy Program oncology clinical trials conducted in the Lombardi Clinical Trials Office of the Lombardi Comprehensive Cancer Center at Georgetown University. Incumbent duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Collaborate with investigators and more senior study team members by participating in recruitment and [. .. ] trials. Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials with Clinical Research Coordinators. Collaborate with Data Coordinator (s) to assure the documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. Document and report serious adverse events per protocol and institutional policy. Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Act [. .. ]
Job am 07.01.2026 bei Neuvoo gefunden
MRI Network
Clinical Research Coordinator
• Östlicher Neubäuer Forst, Bayern
Clinical Research
Coordinator (Onsite) Dallas, TX Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in [...]
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[...] advancing patient care through high-quality, hospital-based clinical trials. The position involves coordinating study activities, collecting data, ensuring compliance, and collaborating with physicians, sponsors, and research teams to keep studies on track and accurate. Company Summary This organization leads with purposeconducting ethical, precise, and innovative clinical research that improves lives. The team is dedicated to advancing healthcare by fostering [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Coordinator pro Jahr?
Als Clinical Trials Coordinator verdient man zwischen EUR 45.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 19 offene Stellenanzeigen für Clinical Trials Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Coordinator Jobs?
Aktuell suchen 10 Unternehmen nach Bewerbern für Clinical Trials Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Coordinator Stellenangebote:
- Georgetown University in Qatar (3 Jobs)
- IQVIA (2 Jobs)
- Milestone One (1 Job)
- PSI CRO (1 Job)
- Green Life Science (1 Job)
- Reesi (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Coordinator Jobs werden derzeit in Baden-Württemberg (4 Jobs), Sachsen (3 Jobs) und Rheinland-Pfalz (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Coordinator Jobs?
Clinical Trials Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
