29 Jobs für Clinical Study Coordinator
Stellenangebote Clinical Study Coordinator Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
Description On-site monitor open to diverse EMEA countries. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and [...]
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[...] commercial insights 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. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] activities in compliance with the Company and Sponsor (if applicable) Standard Operating Procedures (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance depending on assigned study design/ classification. May include Good Pharmacoepidemiology Practices (GPP) and/or International Conference on Harmonization. Good Clinical Practice (ICH-GCP) . Conduct site management activities as per agreed Scope of Work (So W) , Site Management Plan (SMP) and relevant guidelines. Site identification may contact sites to obtain interest in study participation, [. .. ] and experience. Must be proficient in Microsoft Office Suite (Word, Excel, and 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 as well as Real World Research and relevant regulations including GPP. Excellent customer focus (internal and external) and able to interact professionally with a client organization [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Milestone One
Clinical Site Coordinator
• 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 8 Tagen bei Mindmatch.ai gefunden
NÖ Landesgesundheitsagentur
• AT- 3 Amstetten
Abgeschlossene Ausbildung
Eine Gesundheitsagentur in Niederösterreich sucht eine n medizinisch-pflegerische Studienunterstützung (
Study Nurse) , die/ der klinische Studien organisiert und administriert. Zu den Aufgaben gehören die Koordination von Studienprozessen und die Anleitung [...]
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[...] von Patient innen. Anforderungen sind eine abgeschlossene Ausbildung im Gesundheitsbereich sowie Erfahrungen in klinischen Forschungsprojekten. Die Position bietet ein attraktives Vergütungspaket und vielfältige Weiterbildungsmöglichkeiten. J-18808-Ljbffr 84834624 [. .. ]
Job vor 12 Tagen bei Mindmatch.ai gefunden
PSI CRO
Clinical Trials Site Lead
• 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 12 Tagen bei Mindmatch.ai gefunden
PSI CRO
• AT- 9 Wien
Company Description 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 [...]
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[...] sites in stronger study delivery. 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 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 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
Clinical Trials Site Coordinator
• 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 [. .. ]
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 [...]
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[...] in 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
Manager, Clinical Site
• 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. [. .. ] 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 study-specific targets. Support the identification of strategies to expand the research capabilities at the site-in line with the overall site business plan. Support the implementation and maintenance of VCR quality standards at the site ensuring that the conduct of clinical studies and the collection of patient data is in [. .. ]
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 [...]
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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 17.02.2026 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, value-adding solutions and ensuring the adoption of cuttingedge methodologies. Additionally, you will be responsible for developing and executing effective site 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
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 the adoption of cuttingedge methodologies. Additionally, you will be responsible for developing and executing effective site and patient [. .. ] 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
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
• 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 [. .. ]
Job vor 3 Tagen bei Neuvoo.com gefunden
Green Life Science
Clinical Research Coordinator
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-[. .. ] 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, data capture, monitoring, and project management. Having supported 40+ sponsors across the US, UK, and Europe, the organization has successfully delivered studies significantly faster than traditional CRO models, helping accelerate the development of new treatments and therapies. The Role We are seeking an experienced Clinical Research Coordinator [. .. ]
Job vor 7 Tagen bei Neuvoo gefunden
IQVIA
• Trier, Rhineland- Palatinate
[. .. ] gezielt in einer Teilzeitrolle einsetzen? Arbeiten Sie gerne patientennah und strukturiert und legen Wert auf feste Einsatztage? Zur Unterstützung einer laufenden klinischen Studie suchen wir ab sofort [...]
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[...] eine erfahrene:n Studienkoordinator:in/ Clinical Research Coordinator/ Study Nurse (m/w/d) für ein Studienzentrum in Trier. Rahmenbedingungen Arbeitszeit: 16 Stunden pro Woche Einsatztage: Montag und Dienstag Vertragsdauer: ca. 6 Monate Start: kurzfristig möglich Ihre Aufgaben In dieser Rolle übernehmen Sie eine zentrale Funktion im Studienalltag und arbeiten eng mit dem Prüfarztteam zusammen: Koordination und Betreuung einer klinischen [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 guidelines. Coordinate or conduct study-related procedures 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 11 Tagen 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 timelines and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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. [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Reesi
Manager:in Studienzentren Netzwerke
• Hamburg
Flexible Arbeitszeiten
[. .. ] es keine Studien gibt, sondern weil die Strukturen, die passende Studien für Patienten finden sollten, veraltet und fragmentiert sind. Reesi löst genau das. Unsere AI-Plattform ermöglicht es [...]
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[...] Ärzt:innen und Study Nurses in Studienzentren schnell und präzise passende Studien entweder am eigenen Studienzentrum oder in der Umgebung zu finden. Reesi baut die digitale Infrastruktur auf, die ein besseres Studienscreening und effektivere Zusammenarbeit zwischen Studienzentren ermöglicht. Über 1.000 Onkolog:innen in 300+ Kliniken nutzen Reesi bereits. Wir sind ein kleines, ambitioniertes Team [. .. ] 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 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 [. .. ]
Job vor 12 Tagen bei Neuvoo gefunden
Milestone One
Clinical Site Coordinator
• Kassel, Hesse
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 timelines [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
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 work [...]
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[...] 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 written correspondence, status reports to ensure alignment with study timelines. Funtions: Assists in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker plans, and other supporting documents. Create Master ICF template and review/approve site changes (in consultation with legal, safety when warranted) . Update template for [. .. ] 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 [. .. ]
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 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 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 source documents and medical records and completion of case report forms per sponsor requirements. Supports trials of varying complexity and disease indication. Works collaboratively with trial stakeholders and internal study teams (physicians, Regulatory team, Study Coordinators, nursing staff, Research Laboratory Technicians, and Research Pharmacy team) . Reviews and analyzes information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc. ) to extract data for all assigned research protocols-including but not limited to industry, national, and investigator-[. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 guidelines. Coordinate or conduct study-related procedures 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 10.01.2026 bei Neuvoo gefunden
IQVIA
Clinical Research Coordinator/ Study Nurse (m/w/d) in Teilzeit
• Erfurt, Thuringia
Teilzeit
Sind Sie auf der Suche nach einer neuen Chance oder Herausforderung in der klinischen Forschung? Möchten Sie für ein branchenführendes Unternehmen arbeiten? IQVIA sucht derzeit einen
Clinical Research
MEHR INFOS ZUM STELLENANGEBOT
[...] class=highlight_text>Coordinator/
Study Nurse (m/w/d) zur Unterstützung der Durchführung einer klinischen Studie an einem Zentrum in Erfurt. Diese Teilzeit-Position ist ab sofort zu besetzen, zunächst befristet auf ein Jahr. Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den Gesundheits- und Sicherheitsrichtlinien unter der Leitung [. .. ]
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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 29 offene Stellenanzeigen für Clinical Study Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Coordinator Jobs?
Aktuell suchen 13 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:
- IQVIA (6 Jobs)
- Georgetown University in Qatar (3 Jobs)
- Milestone One (2 Jobs)
- PSI CRO (2 Jobs)
- Syneos Health (1 Job)
In welchen Bundesländern werden die meisten Clinical Study Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Study Coordinator Jobs werden derzeit in Baden-Württemberg (5 Jobs), Rheinland-Pfalz (5 Jobs) und Hessen (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Coordinator Jobs?
Clinical Study Coordinator Jobs gehören zum Berufsfeld Medizintechnik.
