21 Jobs für Clinical Trial Coordinator
Stellenangebote Clinical Trial Coordinator Jobs
Job vor 10 Tagen bei Neuvoo gefunden
IQVIA
• Frankfurt, Hessen
Homeoffice möglich
[. .. ] 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 [...]
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[...] team as Experienced Clinical Trial Coordinator (m/w/d) to work in home-office anywhere in Germany. Your responsibilities might include: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e. g. , Trial Master File (TMF) ) that track site compliance and performance [. .. ]
Job am 15.02.2026 bei Neuvoo gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d)
• Karlsruhe, Baden- Württemberg
[. .. ] approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams. Position Overview: As [...]
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[...] a Clinical Trial Coordinator, you will provide administrative and technical support to the Project Team. You will support audit readiness by ensuring files are reviewed on schedule detailed in the organizations WPD and department guidance document. Essential Functions: According to the specific role (Central or Local) , coordinates, oversees and completes functions on assigned [. .. ]
Job gestern bei Jooble gefunden
Hlx Life Sciences
• Berlin
Were working with a CRO whose seeking a Project Manager with 5+ years of CRO project management experience and a strong understanding of the full
clinical trial lifecycle. Lead clinical [...]
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[...] trials from study start-up through closeout-Manage sponsor relationships and cross-functional project teams-Coordinate activities across Clinical Operations and must have strong experience in Medical Writing, Data Management, and Quality Assurance-Ensure compliance with ICH-GCP, regulatory requirements, and company SOPs-Drive project success through [. .. ]
Job am 25.05.2026 bei Mindmatch.ai gefunden
Syneos Health, Inc.
On-site monitor open to diverse EMEA countries
• AT- 9 Wien
[. .. ] (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance for assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference [...]
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[...] on Harmonisation Good Clinical Practice (ICHGCP) . Conduct site management activities as per agreed Scope of Work (So W) , Site Management Plan (SMP) and relevant guidelines. Site identification contact sites to gauge interest, confirm contact details, and obtain relevant documents. Site qualification. Ensure selection of appropriate sites for assigned studies. Site startup with minimal [. .. ] regulatory teams. Conduct all remote and onsite monitoring activities through all study stages. Routinely review the Investigator Site File (ISF) for accuracy, timeliness and completeness; reconcile its contents with the Trial Master File (TMF) ; and ensure sites archive essential documents per local guidelines. Document activities via confirmation letters, followup letters, trip reports, communication logs, and other required project documents per SOPs and SMP; support subject recruitment, retention, and awareness strategies; and enter data into tracking systems to monitor observations, status, [. .. ] equivalent combined education and experience. Proficiency in Microsoft Office Suite (Word, Excel, Power Point) , email/ voicemail, and Clinical Trial Management and EDC systems. Previous site management (inhouse, onsite, study coordinator) or equivalent experience. Excellent communication, time management, organizational, documentation, and customer service skills. Knowledge of local requirements for Real World Late Phase study designs and relevant regulations, including GPP. Excellent customer focus and ability to interact professionally with client organizations and study sites. Willingness to work within a teamoriented environment; [. .. ]
Job am 06.06.2026 bei Jobleads gefunden
• Zug
Milestone One is looking for a Site
Coordinator in Ciudad de Mxico. The successful candidate will support
clinical trial sites by ensuring compliance with ICH-GCP and protocol requirements. Responsibilities include [...]
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[...] acting as the primary communication link between the Sponsor and site, tracking patient enrollment, and facilitating negotiations for contracts. Candidates must have a degree in Life Science, experience in clinical trials, and effective communication skills. This role offers [. .. ]
Job am 05.05.2026 bei Jobleads gefunden
Clinical Trials Lead Site Coordinator
• Zug
Führungs-/ Leitungspositionen
Overview 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 [...]
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[...] in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities 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 [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Job Title: Field
Clinical Research Associate This role supports the Clinical Operations team by overseeing clinical studies, ensuring high-quality human study data collection, and facilitating collaboration between internal study teams, [...]
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[...] contract research organizations, and clinical sites. You will take ownership of site monitoring and study oversight for multiple clinical studies, with a focus [. .. ] study protocols, Good Clinical Practice (GCP) , and ICH guidelines. Collaborate closely with contract research organizations and university sites to facilitate training of site and vendor personnel and support clinical trial execution. Track and maintain regulatory documentation and ensure that all required records are complete, accurate, and up to date. Work with incoming study data to reconcile data reports, identify discrepancies, and generate reports for invoicing and other operational needs. Resolve data queries and delinquencies in a timely manner, coordinating with [. .. ] guidelines relevant to clinical research. Willingness and ability to travel when required for study needs, while supporting primarily virtual monitoring activities. Additional Skills Qualifications Experience similar to a clinical research coordinator, particularly in invoicing, data tracking, and trial closeout activities. Experience working with or for a contract research organization or in a sponsor role supporting clinical studies. Experience in clinical operations, clinical trial execution, or field clinical roles such as Field Clinical Research Manager or Field Clinical Specialist. Exposure to health [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
Global Clinical Operations Lead (m/f/d)
• Luzern
Führungs-/ Leitungspositionen
[. .. ] health. If youre looking to join a successful, global company with real career opportunities, wed love to meet you. About the Role We are seeking an experienced [...]
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[...] and proactive Global Clinical Operations Lead (f/m/d) to manage and oversee clinical trials/ clinical studies/ clinical investigations from initiation to close-out. This role will work closely with GC crossfunctional project teams, investigators, and Contract Research Organizations (CRO) to ensure that studies are conducted in compliance with applicable regulatory requirements, Good Clinical [. .. ] Strong knowledge of clinical investigation processes, GCP, and global regulatory guidelines including ISO14155. Excellent organizational and time management skills. Strong diplomatic and communication skills. Proficiency in Microsoft Office and clinical trial management systems. Excellent command of English is required; knowledge of additional languages will be considered an asset. Willingness to travel internationally as required. Preferred Qualifications Certification as a Clinical Research Coordinator recognized in the US or Europe. Proficiency in class III dental medical devices. Experience with clinical trials preparation, monitoring, tracking and reporting at CRO. Familiarity with electronic medical records (EMR) and patient data privacy regulations (e. g. , EU GDPR, U. S. HIPAA) . Success Metrics Ontime and compliant delivery [. .. ]
Job am 21.05.2026 bei Jobleads gefunden
• Wien
Absolventen, Einsteiger, Trainees
Work-Life-Balance
Study start up CRA, Austria ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome [...]
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[...] you to join us on our mission to shape the future of clinical development. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key Responsibilities Include Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data [. .. ] skills. Required Qualifications And Experience Bachelors degree in a scientific or healthcare-related field. Minimum of 1 year of experience in the clinical research field (e. g. , as Study Coordinator or similar) . In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60) . Fluency in German and English language. What [. .. ]
Job am 14.05.2026 bei Jobleads gefunden
Clinical Research Nurse
• Berlin
Beratungs-/ Consultingtätigkeiten
The
Clinical Research Nurse is responsible for providing clinical nursing care for all study participants an accordance with departmental policies and procedures and established standards of nursing care and [...]
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[...] practice in Clinical Trial setting. Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Job am 05.05.2026 bei Jobleads gefunden
Clinical Research Associate
• Frankfurt, Hesse
Work-Life-Balance
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned [...]
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[...] sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] contact with the site staff, to be aware of patient enrolment, enrolled patients status, IP supply and any further site requests or issues Ensures essential documents are filed in the Trial Master File (TMF) according to the project guidelines Ensures appropriate and timely transmission of clinical data to data management; reviews data queries, and clarifies and/or obtains changes to data as appropriate Conducts site close-out visits to include final IP reconciliation and disposition, review of completeness and accuracy of [. .. ] review process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential. Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trial-related [. .. ]
Job am 03.05.2026 bei Jobleads gefunden
Clinical Research Associate-Germany
• München, Bayern
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned [...]
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[...] sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] contact with the site staff, to be aware of patient enrolment, enrolled patients status, IP supply and any further site requests or issues Ensures essential documents are filed in the Trial Master File (TMF) according to the project guidelines Ensures appropriate and timely transmission of clinical data to data management; reviews data queries, and clarifies and/or obtains changes to data as appropriate Conducts site closeout visits to include final IP reconciliation and disposition, review of completeness and accuracy of files, [. .. ] process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. , Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trialrelated systems [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
• Berlin
The
Clinical Research Nurse is responsible for providing clinical nursing care for all study participants in accordance with departmental policies and procedures and established standards of nursing care and [...]
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[...] practice in Clinical Trial setting. Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Neu Job vor 3 Std. bei Neuvoo gefunden
IQVIA
Clinical Trials Assistant 2 (m/w/d) , based in the Düsseldorf 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 work [...]
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[...] with the preparation and documentation of clinical research projects in different therapeutic areas. We currently offer the exciting opportunity to join the team as Clinical [. .. ] Düsseldorf area. Your responsibilities might include: Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e. g. , Trial Master File (TMF) ) that track site compliance and performance within project timelines. Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for completeness. Assist [. .. ] or pharmaceutical field or office management. At least 2 years of experience as Clinical Trials Assistant or in another administrative role in clinical research, e. g. as Project Assistant, Study Coordinator, Study Nurse. Excellent knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and Power [. .. ]
Job am 07.06.2026 bei Neuvoo gefunden
Subject Well Inc.
• München- Flughafen, Bayern
Freiberuflich
Accelerate patient enrollment in
clinical trials with Subject Well/ Clariness, helping patients gain access to life-changing medications. We support biopharmaceutical companies and CROs in completing clinical trials faster so [...]
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[...] innovative treatments can reach patients sooner. If you enjoy helping people and have strong communication skills, join our virtual team and contribute to meaningful medical research. We are currently seeking a Freelance Study Coordinator to support our team in handling unscripted patient calls related to oncology clinical trials. If you have a medical background, excellent communication skills, and experience in oncology or clinical research, this could be a great fit. Tasks About the role As an Onco-Companion Patient Recruitment, you will serve as a key link between cancer patients, their treating physicians, and clinical trial sites. Your mission is to help patients feel informed and supported as they consider research participation. You will not assess medical eligibility, but rather support understanding, encourage dialogue with care teams, and help coordinate communication with study sites. As an Onco-Companion Patient Recruitment, you will: Conduct unscripted, empathetic conversations [. .. ]
Job am 27.05.2026 bei Neuvoo gefunden
Hays
Contract Coordinator-Clinical Study (m/w/d)
• Monheim am Rhein, North Rhine- Westphalia
Angebote von Zeitarbeitsunternehmen
Contract
Coordinator-Clinical Study (m/w/d) Arbeitnehmerüberlassung Monheim Startdatum: sofort Referenznummer: 878616/ 1 Diesen Job teilen oder drucken Aufgaben Bearbeitung von Anfragenvon Lieferanten, einschließlich Entwurf und Koordination der Prüfung bis zur finalen [...]
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[...] Version Verteilung und Nachverfolgung aller Lieferantenverträge zur internen und externen Unterzeichnung bis zur vollständigen Ausführung, mit Fokus auf elektronische Signaturen [. .. ] deren Verfügbarkeit für relevante Mitarbeitende Anonymisierung von Lieferantenverträgen zum Schutz vertraulicher Informationen, für Inspektionen und Audits Abgleich der Vertragsablage nach Genehmigung des Clinical Study Reports im Rahmen der Archivierungsprozesse des Trial Master File Bereitstellung vertraglicher Informationen auf Anfrage Unterstützung bei Präsentationen und Protokollen Organisation von Meetings sowie Koordination von Büro- und Ausstattungsbedarf Profil Eine abgeschlossene kaufmännische oder naturwissenschaftliche Ausbildung Berufserfahrung in einer Sekretariats-, Verwaltungs-, oder vergleichbaren kaufmännischen Rolle Erfahrung in der Pharma-, Biotechnologie-oder CRO-Branche ist von [. .. ]
Job am 17.05.2026 bei Neuvoo gefunden
Georgetown University in Qatar
• 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 phase I, II and III oncology clinical trials conducted in the Lombardi Clinical Trials Office (Lombardi CTO) at Lombardi Comprehensive Cancer Center. 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 selection of study participants; document and collect data to support protocol screening and determine compliance with eligibility requirements. Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory [. .. ] chart, in compliance with protocol and sponsor requirements. Conduct follow-up with study participants in accordance with established standards and protocols. Provide clinical and administrative nursing support to Clinical Research Coordinator and Clinical Research Nurse positions. Ensure site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities. Coordinate collection of research specimens per protocol requirements with Clinical Research Coordinators. Provide patient education about clinical trial participation, treatment, potential [. .. ]
Job am 14.04.2026 bei Neuvoo gefunden
Parexel
Clinical Research Nurse
• Berlin
When our values align, theres no limit to what we can achieve. The
Clinical Research Nurse is responsible for providing clinical nursing care for all study participants in accordance [...]
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[...] with departmental policies and procedures and established standards of nursing care and practice in Clinical Trial setting. Key Accountabilities : Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Job am 05.04.2026 bei Neuvoo gefunden
PSI
• Kassel, Hessen
Job Description The Milestone One Site
Coordinator role supports a
Clinical Study Site in clinical
trial related activities according to ICH-GCP, protocol requirements within Study specific defined [...]
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[...] timelines and enrollment goals. The function of the role may include, but not limited to, any/ all of the following: Actas the main line of communication between the Sponsor or CRO and the site. Ensureresponse to feasibility questions [. .. ]
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 selection of study participants; document and collect data to support protocol screening and determine compliance with eligibility requirements. Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory [. .. ] 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, [. .. ] This organization leads with purposeconducting ethical, precise, and innovative clinical research that improves lives. The team is dedicated to advancing healthcare by fostering collaboration, scientific excellence, and integrity in every trial conducted. Whats In It for You Be part of meaningful, life-changing research that drives medical progress Enjoy a steady weekday schedule no weekends or holidays Gain hands-on experience with industry-sponsored clinical trials Work in a collaborative, professional environment where your work truly matters Qualifications Bachelors degree required [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Coordinator pro Jahr?
Als Clinical Trial Coordinator verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 21 offene Stellenanzeigen für Clinical Trial Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Coordinator Jobs?
Aktuell suchen 11 Unternehmen nach Bewerbern für Clinical Trial Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Coordinator Stellenangebote:
- IQVIA (2 Jobs)
- Georgetown University in Qatar (2 Jobs)
- Hlx Life Sciences (1 Job)
- Subject Well Inc. (1 Job)
- Hays (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Coordinator Jobs werden derzeit in Bayern (4 Jobs), Sachsen-Anhalt (3 Jobs) und Hessen (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Coordinator Jobs?
Clinical Trial Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
