18 Jobs für Clinical Trial Coordinator
Stellenangebote Clinical Trial Coordinator Jobs
Job am 08.04.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Region Mittlerer Oberrhein, Württemberg; Regierungsbezirk Karlsruhe; Württemberg Karlsruhe, DE
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 future. Location/ Division Specific Information Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, [. .. ]
Job am 06.03.2026 bei Jobleads gefunden
• München, Bayern
[. .. ] an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description Summary Job Description [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] # # ROLEThe Clinical Trial Coordinator assists the clinical research team ensuring to conduct study in accordance to GCP, SOP, protocol, and in respect of budget and timelines. The Clinical Trial Coordinator is responsible of start up activities and documents management. # # KEY RESPONSABILITIES Responsible (under PM oversight) of start up activities, including Ethic [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 gestern bei Mindmatch.ai gefunden
VIROS
• AT- 9 Wien
Das Vienna Institute for Research in Ocular Surgery (VIROS) sucht zur Komplettierung seines Teams einen Back-Office Mitarbeiter in/
Trial Coordinator Clinical Research Associate (m/w/d) . Back-Office Mitarbeiter in/ Trial Coordinator [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Research Associate (m/w/d) 40 Wochenstunden/ 20 Wochenstunden Das erwartet Sie Koordination, Überwachung und Betreuung von klinischen Studien gemäß den gesetzlichen Vorgaben und unter Einhaltung von Studienprotokollen und ethischen Standards Durchführung von Monitoring Besuchen vor Ort [. .. ]
Job gestern bei Mindmatch.ai gefunden
VIROS
• AT- 9 Wien
Ein Institut für Augenforschung in Wien sucht einen Back-Office Mitarbeiterin/
Trial Coordinator Clinical Research Associate, um klinische Studien zu koordinieren und zu überwachen. Voraussetzungen sind sehr gute Kommunikationsfähigkeiten in Deutsch [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] und Englisch sowie Erfahrung in der klinischen Forschung. Angeboten wird eine abwechslungsreiche Tätigkeit in einem jungen Team und die Möglichkeit an internationalen Kongressen teilzunehmen. Das Gehalt beträgt 2.307, 40 EUR brutto pro [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Fortrea
• AT- 9 Wien
Are you detail-oriented and passionate about supporting
clinical research operations? Join our team as an FSP Clinical Project
Coordinator, where youll play a key role in enabling regulatory workflows across [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical studies. This is a sponsor-dedicated, office-based position in Vienna offering meaningful exposure to global clinical development. Key Responsibilities Coordinate administrative tasks related to regulatory submissions. Maintain trackers, logs, and documentation in compliance with internal SOPs and [. .. ] files. Monitor timelines and elevate delays or issues to relevant stakeholders. Contribute to continuous improvement of administrative processes. Required Qualifications At least 1 year of work experience in a clinical trial environment. Some experience in clinical research preferred. Regulatory administrative background. Strong proficiency in Microsoft Office (Excel, Outlook, Word, Power Point) . High affinity for electronic systems and document management tools. Fluent in German and English (verbal and written) . Excellent organizational skills and attention to detail. What We Offer A [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Fortrea
• AT- 9 Wien
Fortrea is seeking an FSP
Clinical Project
Coordinator in Vienna to support clinical research operations. This office-based role involves coordinating regulatory submissions, managing documentation, and liaising with teams to ensure [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] project success. Candidates should have at least 1 year of experience in a clinical trial environment, familiarity with regulatory processes, and strong skills in Microsoft Office. Fluency in German and English is required. Fortrea offers a collaborative work environment and opportunities for professional development. J-18808-Ljbffr 90431007 [. .. ]
Job am 19.03.2026 bei Mindmatch.ai gefunden
Milestone One
• AT- 9 Wien
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] stronger study delivery. Job Description The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICHGCP, protocol requirements within Study specific defined timelines and enrollment goals. The function of the role may include, but not limited to, any/ all of the following: Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility [. .. ]
Job am 19.03.2026 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 within [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites 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 9 Tagen bei Jooble gefunden
Linical
Clinical Research Associate-Germany
• Deutschland Deutschland, DE
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 08.04.2026 bei Jooble gefunden
Clinical Trial Manager/ Local Study Manager
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Clinical Trial Manager/ Local Study Manager Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything [. .. ] Qualifications: Bachelors degree or higher degree in Health or Natural Sciences Three years of experience in clinical research. Experience in project management and certain time as field monitor or site coordinator. International experienced preferred. Fluency in German and English. Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Excellent communication, presentation and interpersonal skills We are always excited to connect with great talent. This posting is intended for a possible upcoming opportunity rather than a live role. By [. .. ]
Job am 08.04.2026 bei Jooble gefunden
R D Where your curiosity drives the miracles of science
• Berlin Berlin, DE
Clinical Operations Study Country Lead-all genders Bring your passion for AI and data-driven thinking to clinical research that makes a real difference. If you re excited about using data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to drive smarter decisions and improve patient lives, we want to meet you About the job Were an R D-[. .. ] (QD) s and ICH/ GCP and regulatory guidelines directives. As Clinical Operations Study Country Lead, you are the strategic hub at country level connecting internal and external stakeholders to accelerate trial execution. You ll collaborate with: Globally: COSL, Data Management, Vendor Management, Study Medical Manager, Clinical Supply Chain Study Manager, Patient Recruitment Retention Lead, and other Core Study Team members Locally: Clinical Research Associates, Clinical Project Assistants, Medical Advisors, Site Engagement Leads, Start-Up Strategy Managers, Medical Science Liaisons, and more [. .. ] medicine, pharmacy, biology, biochemistry or related natural science Experience in clinical research is mandatory, preferably in combination with experience in project management and certain time as field monitor or site-coordinator. Solid knowledge of clinical development process and relevant therapeutic/ disease area (s) ; GCP certificate Soft skills: Strong skills in project management Data analytic skills and use of digital tools, platforms and systems Problem-solving and risk-management skills in a clinical study environment Change management skills Interpersonal skills with [. .. ]
Job am 08.04.2026 bei Jooble gefunden
ICON
Site Engagement Liaison
• Homeoffice Homeoffice, DE
Homeoffice möglich
Work-Life-Balance
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 you to join us [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on our mission to shape the future of clinical development. As a Site Engagement Liaison (SEL) will be responsible for developing relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in pharmaceutical industry clinical trials. You will be partnering with one of the worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and [. .. ] are: Experience in site management, start-up activities to site activation, and close-out activities Exposure to the clinical research environment as a SEL, medical science liaison (MSL) , study coordinator, Senior CRA or experience in a CRO Demonstrated knowledge of quality and regulatory requirements in applicable countries Excellent communication skills in German and English Ability to travel What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build [. .. ]
Job vor 7 Tagen 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 8 Tagen bei Jobleads gefunden
Site Management Associate
• Frankfurt, Hesse
Work-Life-Balance
Clinical Research
Coordinator II ICON plc is a worldleading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Site Management Associate to join our diverse and dynamic team. As a Site Management Associate at ICON, you will play a vital role in supporting the management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will contribute to the efficiency of clinical research operations by providing advanced support to site management teams and fostering strong relationships with site personnel. What You Will Be Doing Coordinating monitoring activities at clinical [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
Clinical Research Nurse
• Berlin
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 12.12.2025 bei Jobleads gefunden
Clinical Project Coordinator
• München, Bayern
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and engage 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 maintain [. .. ]
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 18 offene Stellenanzeigen für Clinical Trial Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Coordinator Jobs?
Aktuell suchen 8 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:
- VIROS (2 Jobs)
- Fortrea (2 Jobs)
- Milestone One (2 Jobs)
- Linical (1 Job)
- Thermo Fisher Scientific (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), Berlin (2 Jobs) und Baden-Württemberg (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Coordinator Jobs?
Clinical Trial Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
