17 Jobs für Clinical Study Coordinator
Stellenangebote Clinical Study Coordinator Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] Responsibilities Perform site management activities in compliance with Company and Sponsor Standard Operating Procedures (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate [...]
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[...] guidance for assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference 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 [. .. ] 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 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 [...]
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[...] 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 external regulations. Support the preparation and review of study-related documentation. Liaise with internal teams to ensure timely updates and data accuracy. Assist in scheduling meetings, managing email communications, and organizing project 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 [. .. ]
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 [...]
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[...] 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 [. .. ]
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 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 [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
• 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 sites, [...]
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[...] ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have [. .. ] 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 24.04.2026 bei Jooble gefunden
Trenkwalder Deutschland
• Region Rhein- Neckar, Württemberg; Regierungsbezirk Karlsruhe; Württemberg Mannheim, DE
Angebote von Zeitarbeitsunternehmen Abgeschlossenes Studium
Weihnachtsgeld Arbeitszeitkonto Übertarifliche Vergütung
Clinical Study Documentation
Coordinator (m/w/d) Unser Kunde, die Roche Diagnostics Gmb H, ist mit rund 15.000 Mitarbeitern (m/w/d) an mehreren Standorten in Deutschland vertreten. Als führendes Unternehmen im Bereich [...]
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[...] der Pharma und Diagnostik entwickelt, produziert und vertreibt unser Kunde Arzneimittel und diagnostische Tests. Das Ziel ist es Krankheiten zu verhindern, [. .. ]
Job am 08.04.2026 bei Jooble gefunden
IQVIA
• Regierungsbezirk Münster; Westfalen Münster, DE
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 Nurse/ [...]
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[...] 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 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
• 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 [...]
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[...] into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. [. .. ] 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
• 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 [...]
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[...] data to drive smarter decisions and improve patient lives, we want to meet you About the job Were an R D-driven, AI-[. .. ] 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
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 [...]
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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 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, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants. Discover Impactful Work: PPD clinical research services mission is to improve health. It starts as an idea to cure. It becomes a life saved. All in-between, [. .. ]
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 [. .. ] this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally. What you will be doing: Work with clinical research associates (CRAs) and the study team to ensure that investigators and site staff have a thorough understanding of the investigational agents being used in the study, the trials eligibility criteria, and all study procedures Responsible for site start-up and activation, for study conduct and close-out and being local expert by providing site recommendations [. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] assigned sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have [. .. ] 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 [. .. ] 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 trial sites, ensuring adherence to study [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 06.03.2026 bei Jobleads gefunden
Clinical Trial Coordinator
• 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 [...]
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[...] # # 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 and Regulatory submission (at national and international level) and [. .. ]
Job am 31.01.2026 bei Jobleads gefunden
Clinical Research Associate III (m/f/d)
• 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 with monitoring systems, data verification, and compliance tracking Strong organizational skills and the ability to manage multiple [. .. ] 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 am 12.12.2025 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 [...]
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[...] 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 [. .. ]
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 17 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:
- Fortrea (1 Job)
- Milestone One (1 Job)
- Linical (1 Job)
- Trenkwalder Deutschland (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 (5 Jobs), Baden-Württemberg (3 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Coordinator Jobs?
Clinical Study Coordinator Jobs gehören zum Berufsfeld Medizintechnik.
