39 Jobs für Research Study Coordinator
Stellenangebote Research Study Coordinator Jobs
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health
• AT- 9 Wien
[. .. ] 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 [...]
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[...] 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 and study site. Willingness to work within a teamoriented environment. Ability to work in a virtual team setting as well as work independently, seeking guidance as appropriate. Ability to handle [. .. ]
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 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 [. .. ]
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 Site Coordinator
• 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 or CRO and the site. Ensureresponse to feasibility questions are provided in due time. Assistin scheduling and preparation for all types of monitoring visits at the medical institution/ research center. Be present and available to respond to monitors duringall types of monitoring visits conducted at the medical institution. Trackpatient enrollment and actively supportthe medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintainstudy specific and general tracking of documents at the site level. Accurate and [. .. ]
Job am 08.03.2026 bei Mindmatch.ai gefunden
Technische Universität Wien
• AT- 9 Wien
TU-ID: 056 2026 09 264469 2 Doctoral Positions (Prae-Doc) 30 hours/ week limited to 4 years TU Wien is Austrias largest institution of
research and higher education in the fields [...]
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[...] of technology and natural sciences. With over 26, 000 students and more than 4000 scientists, research, teaching, and learning dedicated to the advancement of science and technology have been conducted here for more than 200 years, guided by the motto Technology for People. As [. .. ] cutting edge topics High-quality supervision by renowned scientists Continuing personal and professional education Courses on transferable skills Social benefits (e. g. , health insurance, etc. ) Administrative support in study and organizational questions TU Wien is committed to increasing the proportion of women in particular in leadership positions. Female applicants are explicitly encouraged to apply. Preference will be given to women when equally qualified, unless reasons specific to a male applicant tilt the balance in his favour. People with special [. .. ] The article will be sent to the selected candidates one week prior to the hearings. Hearings will be held on June 3, 2026. For further questions please contact the College Coordinator Ivona Brandic, (ivona. brandictuwien. ac. at) , the Co-Coordinator Ioanna Giouroudi (ioanna. giouroudituwien. ac. at) or one of the project leaders. Apply now https:/ / jobs. tuwien. ac. at/ Register/ 264469 If you have any questions, please do not hesitate to contact us Carmen Keck T: +43 1 588 [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Interdisciplinary Transformation University (IT:U)
Study Program Coordinator (f/m/d)
• AT- 4 Linz
Homeoffice möglich
IT:U is a new technical university in Austria (Linz) dedicated to digital transformation, driven by interdisciplinary
research and project-based learning to actively shape this transformation and advance it with a [...]
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[...] solution-oriented approach. Your Tasks And Responsibilities Coordinate courses, faculty, and program administration. Ensure teaching quality, compliance with academic standards, and continuous improvement. Support the Program Committee Chair in curriculum development and strategic alignment. Manage the [. .. ]
Job am 06.03.2026 bei Mindmatch.ai gefunden
Karlstad University
• AT- 4 Linz
Homeoffice möglich
#TRANSFORMINGTOMORROW: MAKE A DIFFERENCE WITH US. IT:U is a new technical university in Austria (Linz) dedicated to digital transformation, driven by interdisciplinary
research and projectbased learning to actively shape [...]
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[...] this transformation and advance it with a solutionoriented approach. For the Ph D program Digital Transformation in Learning Study Program Coordinator (f/m/d) 30h parttime Onsite in Linz (AT) Your tasks and responsibilities: Coordinate courses, faculty, and program administration. Ensure teaching quality, compliance with academic standards, and continuous improvement. Support the Program Committee Chair in curriculum development and strategic alignment. Manage the programs budget and ensure regulatory compliance. Facilitate communication, [. .. ]
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 [...]
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[...] in 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 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 [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• Zürich Zuerich
Call for Predoctoral Fellowships (IMPRS-MDH) Application Deadline: May 31, 2026 Interviews: June 2026 Start: from August 2026 About the IMPRS-MDH The International Max Planck
Research School for Multimodal Digital [...]
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[...] Humanities ( IMPRS-MDH ) is a new doctoral school jointly established by the Bibliotheca Hertziana Max Planck Institute for Art History ( BHMPI ) in Rome and the Faculty of Art and Social Sciences ( Ph F ) of the University of Zurich ( UZH ) [. .. ] a central question: How can the nuanced and culturally diverse patterns of thought and argumentation of the humanities be modelled using AI, and how might we use these models to study both cultural history and the cultural position of AI systems themselves, across languages and cultures? We seek doctoral candidates who bring genuine intellectual investment to one or more of the following research areas, which are not fixed tracks but overlapping problem spaces, we actively encourage proposals that cut across them: [. .. ] Shortlisted candidates will be invited to present their project in an online interview in June 2026. Contact For questions about the program and its research areas, please contact the Scientific Coordinator: Dr. Daro Negueruela del Castillo (DVS/ IMPRS-MDH) , #J-18808-Ljbffr 85444560 [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
Visiting Researchers (f/m/d)
Visiting Researchers Program The Max Planck Institute for the
Study of Societies (MPIf G) conducts basic
research on the governance of modern societies. It aims to develop an [...]
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[...] empirically based theory of the social and political foundations of modern economies by investigating the interrelation between social, economic, and political action. Building on the disciplinary traditions of sociology and political science, the Institutes research program aims to combine [. .. ] belief, disability, age, or sexual orientation or identity. In diversity lies the basis for the cutting-edge research conducted at over 80 Max Planck Institutes. Contact Dr. Mischa Stratenwerth Research Coordinator +49 221 2767 254 March 2026 Max Planck Institute for the Study of Societies Paulstr. 3 50676 Köln Linked In Bluesky #J-18808-Ljbffr 85064986 [. .. ]
Job vor 14 Tagen bei Jobleads gefunden
2 Doctoral Positions (Prae-Doc)
• Wien
TU-ID: 056 2026 09 264469 2 Doctoral Positions (Prae-Doc) 30 hours/ week limited to 4 years TU Wien is Austrias largest institution of
research and higher education in the [...]
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[...] fields of technology and natural sciences. With over 26, 000 students and more than 4000 scientists, research, teaching, and learning dedicated to the advancement of science and technology have been conducted here for more than 200 years, guided by the motto Technology for People. As [. .. ] cutting edge topics High-quality supervision by renowned scientists Continuing personal and professional education Courses on transferable skills Social benefits (e. g. , health insurance, etc. ) Administrative support in study and organizational questions TU Wien is committed to increasing the proportion of women in particular in leadership positions. Female applicants are explicitly encouraged to apply. Preference will be given to women when equally qualified, unless reasons specific to a male applicant tilt the balance in his favour. People with special [. .. ] The article will be sent to the selected candidates one week prior to the hearings. Hearings will be held on June 3, 2026. For further questions please contact the College Coordinator Ivona Brandic, (ivona. brandictuwien. ac. at) , the Co-Coordinator Ioanna Giouroudi (ioanna. giouroudituwien. ac. at) or one of the project leaders. Apply now https:/ / jobs. tuwien. ac. at/ Register/ 264469 If you have any questions, please do not hesitate to contact us Carmen Keck T: +43 1 588 [. .. ]
Job am 08.03.2026 bei Jobleads gefunden
Doctoral Student (m/f/d) for the DFG Research Training Group Organizing Architectures
• Frankfurt, Hesse
Werkstudenten
The Max Planck Institute for Legal History and Legal Theory in Frankfurt/ Main is a world leader in fundamental
research on law. Its three research departments with more than [...]
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[...] 70 scholars, the unrivalled collections of its specialized library, and its numerous national and international co-operations make it the central research hub for a global scientific community investigating the past, present and future of legal regimes. We are looking to [. .. ] of the graduate school and more detailed information on applications can be found at We are also offering an online information event where we will present the research concept, the study program and the future working methods of the college, and will of course be available to answer any questions. Registration is not required. The link to participate can be found on the website mentioned above. Your profile We welcome applications that demonstrate a serious interest in legal history or in [. .. ] of June 2026. Contact Informal enquiries may be directed to PD Dr. Peter Collin or-as far as it generally concerns the activities of the Research Training Group to the coordinator of the research training group, Friederike Weidner. For questions as to the terms and conditions of employment please contact Anna Heym. #J-18808-Ljbffr 83340879 [. .. ]
Job am 08.03.2026 bei Jobleads gefunden
2 Doctoral Positions (Prae-Doc)
• Wien
TU-ID: 056 limited to 4 years TU Wien is Austrias largest institution of
research and higher education in the fields of technology and natural sciences. With over 26, 000 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] students and more than 4000 scientists, research, teaching, and learning dedicated to the advancement of science and technology have been conducted here for more than 200 years, guided by the motto Technology for People. As [. .. ] cutting edge topics High-quality supervision by renowned scientists Continuing personal and professional education Courses on transferable skills Social benefits (e. g. , health insurance, etc. ) Administrative support in study and organizational questions TU Wien is committed to increasing the proportion of women in particular in leadership positions. Female applicants are explicitly encouraged to apply. Preference will be given to women when equally qualified, unless reasons specific to a male applicant tilt the balance in his favour. People with special [. .. ] The article will be sent to the selected candidates one week prior to the hearings. Hearings will be held on June 3, 2026. For further questions please contact the College Coordinator Ivona Brandic, ( ) , the Co-Coordinator Ioanna Giouroudi ( ) or one of the project leaders. https:/ / jobs. tuwien. ac. at/ Register/ 264469 In your application, please refer to my Science. at and reference Job ID48803. #J-18808-Ljbffr 83339485 [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our values and behaviors to give our employees the best chance of delivering on our brand promise: to bring innovative medical treatments to patients. We [. .. ] 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
[. .. ] 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
[. .. ] 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 [...]
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[...] 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 [. .. ] medication, etc. Oversee service providers to ensure successful implementation within agreed timelines, budget, and quality. Develop and implement a monitoring strategy in collaboration with Clinical Trial Leads (CTLs) and Contract Research Organizations (CROs) , using a riskbased quality management approach. Continuously update the strategy based on external changes and new internal data. Utilize site performance and quality data analytics to drive proactive, riskbased site oversight practices and quality risk oversight and management across all stages of study delivery. Develop, implement, 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
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] medication, etc. Oversee service providers to ensure successful implementation within agreed timelines, budget, and quality. Develop and implement a monitoring strategy in collaboration with Clinical Trial Leads (CTLs) and Contract Research Organizations (CROs) , using a riskbased quality management approach. Continuously update the strategy based on external changes and new internal data. Utilize site performance and quality data analytics to drive proactive, riskbased site oversight practices and quality risk oversight and management across all stages of study delivery. Develop, implement, 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. 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 12.02.2026 bei Jobleads gefunden
Doctoral candidate for Broadband Packaging of SiC optical frequency combs
• Villigen, Aargau
[. .. ] team as a doctoral candidate. This position is part of Silicon carbide photonic integrated circuit (Si CPIC) , a prestigious European Doctoral Network project funded by the [...]
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[...] European Unions Horizon Europe Research and Innovation Programme under the Marie Skodowska-Curie Action (MSCA) , Grant Agreement No. 101227010. Project Context The Si CPIC project aims at developing next-generation PIC technologies by unlocking the unique optical properties of Silicon carbide (Si C) . One example is the Si C based optical frequency comb (OFC) with low [. .. ] and the candidate will be enrolled in one of the general degree programs at Polytechnic University of Turin. For information about enrolment requirements and the general planning of the Ph D study program, please see the Politecnico di Torino Doctoral School website. Diversity Swiss PIC is committed to diversity at the workplace. With us you will find an open, multicultural environment. Excellent flexible working arrangements enable all genders to strike the desired balance between their professional development and their personal lives. All [. .. ] will be informed by email within two work weeks on the outcome. The following interviews and selection process will be carried out by a temporary Selection Committee constituted by the Coordinator (when possible) and the supervisors. Evaluation criteria include: Scientific background, capacity for creativity and independent thinking and leadership, mentoring and presentation abilities. #J-18808-Ljbffr 80493913 [. .. ]
Job am 08.02.2026 bei Jobleads gefunden
• Basel, Basel- Stadt
[. .. ] the University of Basel offers doctoral students excellent conditions for writing their dissertations in literary studies and closely related fields. Selected seminars, regular doctoral colloquia, as well [...]
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[...] as retreats and study days provide opportunities to exchange ideas, receive feedback on work in progress, and acquire skills for an academic career. The Program also supports members with contributions to conferences, research trips, archival travel and financial support for their own events. The Start-Up Grant The one-year start-up grant (application deadline: April 12, 2026; start date: October 1, 2026) is intended to contribute to living expenses during the elaboration phase of a dissertation project in literary studies. The aim [. .. ] must present a confirmation of supervision no later than the interview. Read our website carefully. The following documents should be sent in electronic form (collected in one PDF) to the coordinator of the Doctoral Program in Literary Studies: by April 12, 2026: letter of motivation curriculum vitae (with list of publications, if applicable) outline of the dissertation project (max. 5 pages plus bibliography) degree certificate with final grade (MA degree or equivalent; if the certificate is not yet available, include a [. .. ]
Job am 31.01.2026 bei Jobleads gefunden
Clinical Research Associate III (m/f/d)
• Stein, Baden- Württemberg
[. .. ] 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 are [...]
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[...] 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 [. .. ] Degree preferred; Excellent oral and written English Language communication skills, German knowledge desirable; Knowledge of Microsoft Office programs; Experience in a health sciences or business setting preferred; Experience in clinical research is preferred but not required; Excellent organisational and prioritisation skills; Strong attention to detail; We kindly ask you to attach a cover letter and submit your application in English. Medpace Overview Medpace is a fullservice clinical contract research organisation (CRO) . We provide Phase IIV clinical development services to the [. .. ]
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 next-generation, full-service [...]
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[...] 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
Studienkoordinator:in/ Clinical Research Coordinator/ Study Nurse (m/w/d)
• Trier, Rhineland- Palatinate
[. .. ] 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 eine [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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
[. .. ] 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 [...]
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[...] 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
Clinical Site Coordinator.
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 or CRO and the site. Ensureresponse to feasibility questions are provided in due time. Assistin scheduling and preparation for all types of monitoring visits at the medical institution/ research center. Be present and available to respond to monitors duringall types of monitoring visits conducted at the medical institution. Trackpatient enrollment and actively supportthe medical site and CRO/ Sponsor team in meeting project timelines and enrollment goals. Maintainstudy specific and general tracking of documents at the site level. Accurate and [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Research Study Coordinator pro Jahr?
Als Research Study Coordinator verdient man zwischen EUR 45.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Research Study Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 39 offene Stellenanzeigen für Research Study Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Research Study Coordinator Jobs?
Aktuell suchen 18 Unternehmen nach Bewerbern für Research Study Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Research Study Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Research Study Coordinator Stellenangebote:
- IQVIA (6 Jobs)
- Georgetown University in Qatar (3 Jobs)
- Milestone One (2 Jobs)
- Syneos Health (1 Job)
- PSI CRO (1 Job)
In welchen Bundesländern werden die meisten Research Study Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Research Study Coordinator Jobs werden derzeit in Baden-Württemberg (6 Jobs), Hessen (5 Jobs) und Rheinland-Pfalz (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Research Study Coordinator Jobs?
Research Study Coordinator Jobs gehören zum Berufsfeld Forschung, Lehre, Wissenschaft.
