43 Jobs für Clinical Study Coordinator
Stellenangebote Clinical Study Coordinator Jobs
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• Wiesbaden
Work-Life-Balance
[. .. ] experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] is preferred. Current knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Freiberuflich
[. .. ] groundbreaking medical research and make a real impact? Join our client and lead the way in advancing clinical research Proclinical is supporting a client who is seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an experienced Freelance Clinical Study Coordinator for an on-site assignment in North Rhine-Westphalia, Germany. This is a 6-month freelance contract, with the possibility of renewal, requiring 2-3 days per week on site, with an immediate start date. Responsibilities Clinical data entry Query resolution Management of patient travel cost reimbursement Key Skills and [. .. ]
Job am 24.01.2026 bei Neuvoo gefunden
Proclinical
Freelance Clinical Research Coordinator
• Düsseldorf, North Rhine- Westphalia
Freiberuflich
[. .. ] groundbreaking medical research and make a real impact? Join our client and lead the way in advancing clinical research Proclinical is supporting a client who is seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] an experienced Freelance Clinical Study Coordinator for an on-site assignment in North Rhine-Westphalia, Germany. This is a 6-month freelance contract, with the possibility of renewal, requiring 2-3 days per week on site, with an immediate start date. The main responsibilities include: Clinical data entry Query resolution Management of patient travel cost reimbursement [. .. ]
Job vor 3 Tagen bei Jooble gefunden
Kantonsspital Aarau AG
• Schweiz
# # #BL/ BL # # #
Clinical Research
Coordinator (Datamanagement) Clinical Research Coordinator (Datamanagement) KSA Kinderspital Aarau, Pädiatrische Hämatologie und Onkologie Startdatum Ab 1. April 2026 oder nach Vereinbarung, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] unbefristet Pensum 40-60 Arbeitsort Aarau Ihre Aufgaben Koordination/ Datamanagement von klinischen Studien und wissenschaftlichen Projekten am Universitären Zentrum für Pädiatrische Hämatologie und Onkologie Nordwestschweiz, Standort Kinderspital Kantonsspital Aarau Vorbereitung, [. .. ] u. a. ) Ihr Profil Ausbildung/ Tätigkeit im Gesundheitswesen (z. B. Pflegefachperson, MPA) , naturwissenschaftlicher Hintergrund (z. B. Biomedizin, Phar-mazie) oder Qualitätsmanagement Weiterbildung/ Erfahrung als Clinical Research Coordinator oder Study Nurse von Vorteil Sorgfältige, zuverlässige und selbständige Arbeitsweise Sicherer Umgang mit digitalen Dokumentationssystemen Deutschkenntnisse in Wort und Schrift, Englischkenntnisse unerlässlich Teamfähigkeit, vernetztes Denken und hohe Sozialkompetenz im Kontakt mit internen und externen Stellen Ihre Vorteile Das Kantonsspital Aarau führt eine eigene Tagesstätte für Kinder von Mitarbeitenden zwischen 0 und 12 [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d) - Germany
• Karlsruhe
[. .. ] 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, 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 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
Regional Clinical Operations Manager
• München
Milestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites in stronger [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study delivery. Job Description As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. This is a regional role, with the region [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
• München
Milestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites in stronger [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study delivery. As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. Take end-to-end operational responsibility for clinical [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Senior Site Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model
• München
Führungs-/ Leitungspositionen
Senior Site Contracts Lead (Multiple location: 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 that we do. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] subject matter expert within the organization equipped to help resolve global site contracting issues, and escalation point within the Company for internal customers to seek assistance. Oversees negotiations of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract budget negotiators. Advises study team and Sponsor stakeholders on industry trends, norms, and emergent developments surrounding site contract [. .. ] . BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/ pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Proficient in MS Office (Word, Excel and Power Point) , MS Project, outlook and Internet. Ability to handle multiple tasks to meet deadlines, delivering high quality work in [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
• Homeoffice
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 on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 am 14.01.2026 bei Jooble gefunden
IQVIA
Clinical Research Coordinator/ Study Nurse (m/w/d) - Neuwied
• Koblenz
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 Neuwied. Diese Position ist ab sofort zu besetzen, zunächst befristet auf 6 Monate. Der Umfang beträgt 24 Stunden pro Woche. Zu den täglichen Aufgaben gehören: Koordinierung klinischer Forschungsstudien und Aufrechterhaltung eines sicheren Studienumfelds gemäß den [. .. ]
▶ Zur Stellenanzeige
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Münster
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Nurse/ 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 14.01.2026 bei Jooble gefunden
IQVIA
Study Nurse (m/w/d)
• Mannheim
Homeoffice möglich
[. .. ] unerwünschten Ereignissen und Produktbeschwerden gemäß den geltenden Anforderungen verantwortlich. Das bringen Sie mit: Examinierte Krankheits- und Gesundheitspfleger/-in oder eine gleichwertige Ausbildung mit mindestens 1 Jahr Berufserfahrung Erfahrung [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] in Studien (Study Nurse/ Study Coordinator) Sehr gutes Verständnis und allgemeine Kenntnisse des Gesundheitswesens Flexibilität (neue Projekte, Arbeitszeit) Sie organisieren Ihren Arbeitsalltag gerne eigenverantwortlich Sie sind ein echter Teamplayer und pflegen gerne nachhaltige Beziehungen zu ihren Ansprechpartnern Das bieten wir Ihnen: Ein attraktives Gehaltspaket Firmen PKW auch zur Privatnutzung (ohne Zuzahlung) Moderne IT-Ausstattung Attraktive Sozialleistungen [. .. ] Bewerbung per Mail an: click to reveal email address #LI-CES #LI-DNP #LI-SS2 #Nurses #Field Nurse IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at 76125238 [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
• Mannheim, Baden- Württemberg
Ready to be the heartbeat of medical research? Join our client as a
Study Coordinator and assist in turning innovative science into life-changing care R D Partners is seeking a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Clinical Research Associate to support the planning, coordination, and execution of clinical research studies. You will work closely with study sites to ensure compliance with protocols, regulations, and best practices. This role involves collaboration with cross-functional teams and offers an opportunity to contribute to impactful research projects. Please note that [. .. ]
Job vor 8 Tagen 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 vor 11 Tagen bei Jobleads gefunden
Clinical Research Associate III (m/f/d)
• Hechingen, 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 CRAs are expected to guide junior team members Hands-on 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 19.01.2026 bei Jobleads gefunden
Regional Clinical Operations Manager
• München, Bayern
Milestone One is a Site Enabling Organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites in stronger [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] study delivery. Job Description As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, lead site operations, manage coordinator teams, and ensure that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a handson leader with deep knowledge of clinical trial operations who can proactively identify and resolve daytoday challenges in a dynamic international environment. This is a regional role, with the region to be assigned. [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Clinical Research Associate III
• Berlin
[. .. ] counts, 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We are hiring 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 purposedriven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure to [. .. ]
Job am 19.01.2026 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 [...]
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 and Regulatory submission (at national and international level) and [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Senior Site Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] January 14, 2026 Location: Munich, Germany Job ID: 25104919-OTHLOC-3530-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and 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 [. .. ] subject matter expert within the organization equipped to help resolve global site contracting issues, and escalation point within the Company for internal customers to seek assistance. Oversees negotiations of clinical study agreements (CTAs) on a study level and drives CTA document finalization and execution, including contractual language terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract budget negotiators. Provides oversight of contact budget negotiations status and manages escalation of out-of-parameter queries on [. .. ] Qualifications BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/ pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Strong presentation, documentation and interpersonal skills. Proficient in MS Office (Word, Excel and Power Point) , MS Project, Outlook and Internet. Ability to handle multiple tasks to meet [. .. ]
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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 43 offene Stellenanzeigen für Clinical Study Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Study Coordinator Jobs?
Aktuell suchen 14 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:
- Abb Vie (6 Jobs)
- IQVIA (6 Jobs)
- Milestone One (3 Jobs)
- Georgetown University in Qatar (3 Jobs)
- Thermo Fisher Scientific (2 Jobs)
- Kantonsspital Aarau AG (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 (10 Jobs), Baden-Württemberg (5 Jobs) und Rheinland-Pfalz (4 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Study Coordinator Jobs?
Clinical Study Coordinator Jobs gehören zum Berufsfeld Medizintechnik.
