Clinical Research Coordinator Stellenangebote


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Stellenangebote Clinical Research Coordinator Jobs


Job am 08.04.2026 bei Jooble gefunden IQVIA

Clinical Research Coordinator (m/w/d) - Teilzeit in Münster

• Regierungsbezirk Münster; Westfalen Münster, DE Teilzeit [. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Study 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 [. .. ]

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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 welcome you [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to join us on our mission to shape the future of clinical development. We are currently seeking a Site Management Associate to join [. .. ]

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Job am 18.04.2026 bei Jobleads gefunden

Clinical Research Nurse

• Berlin [. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 [. .. ]

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Job vor 4 Tagen bei Aktuelle TopJobs gefunden Deutsche Rentenversicherung Baden- Württemberg Sachbearbeiter/in Projektbüro (m/w/d) • Karlsruhe oder Stuttgart Sachbearbeiter/in Projektbüro (m/w/d) Deutsche Rentenversicherung Baden-Württemberg Karlsruhe oder Stuttgart Die Deutsche Rentenversicherung (DRV) Baden Württemberg ist einer der größten Regionalträger der gesetzlichen Rentenversicherung mit rund 3.600 Mitarbeitenden. Unsere Digitalisierungsabteilung stellt [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Anwenderinnen und Anwendern ein breit [. .. ]

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Job gestern bei Mindmatch.ai gefunden VIROS

Back-Office Mitarbeiterin/ Trial Coordinator Clinical Research Associate (m/w/d)

• 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 [. .. ]

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Job gestern bei Mindmatch.ai gefunden VIROS Clinical Research Trial Coordinator CRA • 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 Monat. [. .. ]

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Job vor 7 Tagen bei Mindmatch.ai gefunden Fortrea

FSP Clinical Project Coordinator based in Vienna

• 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 [. .. ]

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Job vor 7 Tagen bei Mindmatch.ai gefunden Fortrea Vienna Office: Clinical Project Coordinator for Regulatory Submissions • 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. [. .. ]

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Job am 19.03.2026 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 [...]
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 questions are provided in due time. Assist in scheduling and preparation for all types of monitoring visits at the medical institution/ research center. Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution. Track patient enrollment and actively support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the [. .. ]

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Job vor 5 Tagen bei Jobleads gefunden Clinical Trials Lead Site Coordinator • Zug Führungs-/ Leitungspositionen Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites [...]
MEHR INFOS ZUM STELLENANGEBOT[...] 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 for all types of monitoring visits at the medical institution/ research center. Be present and available to respond to monitors during all types of monitoring visits conducted at the medical institution. Track patient enrollment and actively support the medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the [. .. ]

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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 sites, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source [. .. ] 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 [. .. ]

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Job vor 11 Tagen bei Jooble gefunden EVIDENT Europe GmbH HR Business Partner (m/f/d) • Hamburg Hamburg, DE [. .. ] total of 57 locations worldwide. Evident Europe, headquartered in Hamburg, Germany, employs approximately 770 people in 16 countries. The product portfolio includes a wide range of microscope [...]
MEHR INFOS ZUM STELLENANGEBOT[...] systems used in clinical diagnostics, medical and basic research, as well as in various industrial areas. In addition, Evident offers videoscopes, products for non-destructive testing techniques and for X-ray fluorescence analysis. As HRBP you will act as a trusted advisor to managers and employees across the EMEA region, driving the full spectrum of HR activities and ensuring [. .. ] and compensation reviews. Provides advice and day-to-day HR support on operational topics (e. g. , parental leave, onboarding, new starter introductions) , in close collaboration with the HR Coordinator. Supports managers with personnel and organizational matters, including fixed-term contracts, extensions, job postings, and related administrative processes. Acts as the primary contact for external service providers and institutions (e. g. , laborlawyers, relocation services, occupational health and safety authorities, immigration offices) Continuously reviews, optimizes, and documents HR processes, ensuring [. .. ]

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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 [. .. ] conduct and leads a study team through change management efforts and by example. 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 [. .. ]

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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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] data to drive smarter decisions and improve patient lives, we want to meet you About the job Were an R D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of [. .. ] 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 [. .. ]

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Job am 08.04.2026 bei Jooble gefunden Thermo Fisher Scientific

Clinical Trial Coordinator II (m/f/d)

• Region Mittlerer Oberrhein, Württemberg; Regierungsbezirk Karlsruhe; Württemberg Karlsruhe, DE [. .. ] our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] step beyond through research, development and delivery of life-changing 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 [. .. ]

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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 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 to [. .. ] 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 [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden

Business Process

• Hamburg Homeoffice möglich [. .. ] Team Assistant Finance Operations übernimmst du eine zentrale Rolle in unserem Germany Value and Risk Advisory (VRA) Team. Business Operations Assistant (m/w/d) Darmstadt Reporting directly to the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Workplace Coordinator, the Office Services Assistant will provide exceptional customer service to both internal and external customers. To go above and beyond, making our guests feel welcome and comfortable. Clinical Trials Assistant 1 (m/w/d) Frankfurt, Hesse, Germany We currently offer the exciting opportunity to join the team as Clinical Trials Assistant 1/ CTA I (m/w/d) in fulltime and work officebased in our Germany headquarter in Frankfurt. Occasional homeoffice is possible after onboarding. Administrative Assistant for the [. .. ] Assistant technologies (e. g. Google Dialogflow, IBM Watson) Experience with cloud services such as AWS, GCP or Azure Knowledge of Agile/ Dev Ops software development (Git Ops is a plus) Research Assistant (Post Doc) in the field of additive manufacturing of metals Wuppertal Bergische Universität Wuppertal sucht in eine/n Research Assistant (Post Doc) in the field of additive manufacturing of metals (ID-Nummer: 13962031) . Facility Administrative Assistant Southbridge Your Profile High School Diploma or equivalent Minimum three (3) years [. .. ]

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Job vor 6 Tagen bei Jobleads gefunden Projektmitarbeiter der Geschäftsführung (m/w/d) Vollzeit in München • München, Bayern Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium Betriebliche Altersvorsorge [. .. ] chances of interviewing at BONAGO Incentive Marketing Group by 2x Get notified about new Project Associate jobs in Munich, Bavaria, Germany. Junior Project Manager/ PMO (all genders) [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Tester for a car voice assistant project-English (Australian) speaker Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Supply Chain Project Coordinator (m/f/d) Product Process Support Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Junior Projektmanager Elektrotechnik (all gender) Working Student Smart Site Operations Strategy (m/f/d) Intern Sustainability Management (f/m/d) Working Student Medical ML Data Management (f/m/x) Project Manager-Employee Research/ Surveys Tester for a car voice assistant project-French (France) speaker Strategic Project Assistant to CSMO (m/w/d) Working Student: Product Management and Data Analyst Associate (f/m/div) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of [. .. ]

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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 sites, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source [. .. ] 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 [. .. ]

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Job vor 11 Tagen bei Jobleads gefunden Responsable de psychologues spcialiss ou spcialises en psychothrapie-Crans-Montana-80 • Crans- Montana, Wallis Join HUG as a specialized psychotherapist in Crans-Montana. Enjoy a supportive work environment with great benefits. Tasks Supervise clinical evaluations and psychotherapeutic activities. Coordinate training for trainee psychologists and [...]
MEHR INFOS ZUM STELLENANGEBOT[...] interns. Contribute to the development of rehabilitation care programs. Skills Masters in psychology and federal specialist title in psychotherapy required. Strong communication and organizational skills needed. Experience in psychosomatic rehabilitation is a plus. Job Description Reporting to the units responsible physician, you are part of the services management team and work closely with all professionals, as well as with the institutional coordinator of the psychologists network. As a psychologist expert, you put your expertise at the service of the team and ensure the transmission of knowledge. You supervise clinical assessments, psychotherapeutic activities, and the continuing education of psychologists. In this capacity, you organize their scheduling, ensure the quality of case followup, compliance [. .. ] well as to the implementation of evaluation systems within the service. In collaboration with the services professionals, you initiate, coordinate, and participate in undergraduate and postgraduate teaching activities. You lead research projects related to the services focus areas and support, when applicable, staff mandated for public or private research. Clinically, you assess the psychological functioning of patients, address their difficulties, and develop appropriate intervention plans. You develop therapeutic and preventive actions promoting proactive care. Your activity is part of a strong [. .. ]

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Job am 28.03.2026 bei Jobleads gefunden MSW Program Director Associate/ Professor (Online) • Steiermark Führungs-/ Leitungspositionen [. .. ] Division Division Academic Division Location Location WZ 209 Link to Department Website or Custom Search Page Position Summary, Requirements, and Qualifications Position Summary, Requirements, and Qualifications Overview [...]
MEHR INFOS ZUM STELLENANGEBOT[...] The School of Clinical and Developmental Sciences in the College of Health and Human Sciences at Northern Illinois University invites applications for a full-time, 9-month, Associate Professor or Professor to serve as the inaugural Master of Social Work ( MSW ) Program Director and provide visionary leadership to develop the MSW program [. .. ] a commitment to NIUs mission by supporting access to high-quality education, mentoring faculty, and developing partnerships with community-based organizations while directing the program. NIU is a Carnegie Doctoral/ Research University-High Research Activity located in De Kalb, IL. The main campus is in De Kalb, which is a diverse and growing community, 65 miles west of Chicagos Loop and 40 miles southeast of Rockford with education centers in Rockford and Naperville. De Kalb County, with a population of about [. .. ] and orders pertaining to nondiscrimination, equal opportunity and affirmative action. The following person has been designated to handle inquiries regarding the non-discrimination policies: Ethics and Compliance Officer, Title IX Coordinator Health Services Building Room 230 815-753-5560 In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. ADA Accommodation NIU remains committed to ensuring that [. .. ]

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Job am 28.03.2026 bei Jobleads gefunden Associate Professor/ Professor and Master of Social Work (MSW) Program Director (6363) • Steiermark Führungs-/ Leitungspositionen [. .. ] (6363) Faculty, School of Clin Devl Sciences, College of Health and Human Sciences, Northern Illinois University Position: Full-Time; 9-month; FTE 1.00; Exempt Position Summary The School of [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Clinical and Developmental Sciences in the College of Health and Human Sciences at Northern Illinois University invites applications for a full-time, 9-month, Associate Professor or Professor to serve as the inaugural Master of Social Work ( MSW ) Program Director and provide visionary leadership to develop the MSW program [. .. ] a commitment to NIUs mission by supporting access to high-quality education, mentoring faculty, and developing partnerships with community-based organizations while directing the program. NIU is a Carnegie Doctoral/ Research University-High Research Activity located in De Kalb, IL. The main campus is in De Kalb, which is a diverse and growing community, 65 miles west of Chicagos Loop and 40 miles southeast of Rockford with education centers in Rockford and Naperville. De Kalb County, with a population of about [. .. ] pertaining to nondiscrimination, equal opportunity and affirmative action. Discrimination Policies The following person has been designated to handle inquiries regarding the non-discrimination policies: Ethics and Compliance Officer, Title IX Coordinator Health Services Building Room 230 815-753-5560 ADA Accommodation NIU remains committed to ensuring that its recruitment and application procedures include full opportunities for applicants with disabilities. Employment opportunities will not be denied to anyone because of the need to make accommodations for a persons disability during either the [. .. ]

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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 [...]
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 [. .. ]

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Job am 22.02.2026 bei Jobleads gefunden School Psychologist (2026-27) • Unterseen, Bern [. .. ] District level committees Communicates psychological principles and information in a useable and practical manner for broad use with schools or systems Participates in activities that promote professional [...]
MEHR INFOS ZUM STELLENANGEBOT[...] development and uses clinical/ educational research to enhance therapy services Provides immediate supervision of school psychologist interns and support staff, when applicable. Uses effective and current teaching techniques and feedback processes in instructing interns Makes certain interns are oriented to department practices and activities Provides regular supervision and consultation Actively assesses progress of interns skills and [. .. ] District. EEO Statement St. Cloud School District 742 prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to the Title IX Coordinator. The notice of nondiscrimination is located at https:/ / For inquiries, please contact #J-18808-Ljbffr 81608418 [. .. ]

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Job am 20.02.2026 bei Jobleads gefunden School Psychologist-Part-time (2026-27) • Unterseen, Bern [. .. ] District level committees Communicates psychological principles and information in a useable and practical manner for broad use with schools or systems Participates in activities that promote professional [...]
MEHR INFOS ZUM STELLENANGEBOT[...] development and uses clinical/ educational research to enhance therapy services Provides immediate supervision of school psychologist interns and support staff, when applicable Uses effective and current teaching techniques and feedback processes in instructing interns Makes certain interns are oriented to department practices and activities Provides regular supervision and consultation Actively assesses progress of interns skills and [. .. ] the needs of the District. St. Cloud School District742 prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to the Title IX Coordinator. The notice of nondiscrimination is located athttps:/ / For inquiries, please contact #J-18808-Ljbffr 81310225 [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Clinical Research Coordinator pro Jahr?

Als Clinical Research Coordinator verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Clinical Research Coordinator Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 28 offene Stellenanzeigen für Clinical Research Coordinator Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Research Coordinator Jobs?

Aktuell suchen 11 Unternehmen nach Bewerbern für Clinical Research Coordinator Jobs.


Welche Unternehmen suchen nach Bewerbern für Clinical Research Coordinator Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Research Coordinator Stellenangebote:


  • VIROS (2 Jobs)
  • Fortrea (2 Jobs)
  • Milestone One (1 Job)
  • Linical (1 Job)
  • EVIDENT Europe GmbH (1 Job)


In welchen Bundesländern werden die meisten Clinical Research Coordinator Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Research Coordinator Jobs werden derzeit in Bayern (6 Jobs), Niedersachsen (4 Jobs) und Baden-Württemberg (2 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Research Coordinator Jobs?

Clinical Research Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.


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