15 Jobs für Clinical Systems Coordinator
Stellenangebote Clinical Systems Coordinator Jobs
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 [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
• AT- 9 Wien
[. .. ] (SOPs) and Work Instructions (WIs) . Assure compliance with local regulations and appropriate guidance for assigned study design/ classification, including Good Pharmacoepidemiology Practices (GPP) and International Conference [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on Harmonisation Good Clinical Practice (ICHGCP) . Conduct site management activities as per agreed Scope of Work (So W) , Site Management Plan (SMP) and relevant guidelines. Site identification contact sites to gauge interest, confirm contact details, and obtain relevant documents. Site qualification. Ensure selection of appropriate sites for assigned studies. Site startup with minimal [. .. ] via confirmation letters, followup letters, trip reports, communication logs, and other required project documents per SOPs and SMP; support subject recruitment, retention, and awareness strategies; and enter data into tracking systems to monitor observations, status, and action items. Demonstrate diligence in protecting the confidentiality of each subject or patient. Review assigned site data, assist with data query resolution and missing data followup; analyze data using trend reports and site practices; ensure timely resolution of data queries; and use available hardware and [. .. ] equivalent combined education and experience. Proficiency in Microsoft Office Suite (Word, Excel, Power Point) , email/ voicemail, and Clinical Trial Management and EDC systems. Previous site management (inhouse, onsite, study coordinator) or equivalent experience. Excellent communication, time management, organizational, documentation, and customer service skills. Knowledge of local requirements for Real World Late Phase study designs and relevant regulations, including GPP. Excellent customer focus and ability to interact professionally with client organizations and study sites. Willingness to work within a teamoriented environment; [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Fortrea
• AT- 9 Wien
Are you detail-oriented and passionate about supporting
clinical research operations? Join our team as an FSP Clinical Project
Coordinator, where youll play a key role in enabling regulatory workflows across [...]
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 [. .. ] experience in a clinical trial environment. Some experience in clinical research preferred. Regulatory administrative background. Strong proficiency in Microsoft Office (Excel, Outlook, Word, Power Point) . High affinity for electronic systems and document management tools. Fluent in German and English (verbal and written) . Excellent organizational skills and attention to detail. What We Offer A collaborative and inclusive work environment. Opportunities for professional development in clinical operations. Client-office-based role in Vienna with structured onboarding and training. Employee resource groups [. .. ]
Job am 19.03.2026 bei Mindmatch.ai gefunden
Milestone One
• AT- 9 Wien
Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites in [...]
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 [. .. ] Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the site level. Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations. Proper handling, accountability and reconciliation of investigational products and clinical supplies. Collect, handle and maintain all sitespecific regulatory documents as needed. Facilitate and support the contract and [. .. ]
Job vor 5 Tagen bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites [...]
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 [. .. ] Sponsor team in meeting project timelines and enrollment goals. Maintain study specific and general tracking of documents at the site level. Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. Timely reporting and follow up on Reportable Adverse Events and Protocol Deviations. Proper handling, accountability and reconciliation of investigational products and clinical supplies. Collect, handle and maintain all site-specific regulatory documents as needed. Facilitate and support the contract [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
• Deutschland Deutschland, DE
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned sites, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] review of completeness and accuracy of files, and retrieval of documents for the TMF; prepares site close-out visit reports and associated documentation Attend team meetings as required Participates in systems User Acceptance Testing as required Senior CRA assists with the development and implementation of study-specific monitoring and reporting procedures, methods, guidelines, and tools; participates in development of participant tracking systems; conducts monitoring assessment visits for the purpose of rescuing a troubled site or performing audit preparation at the direction [. .. ] process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. , Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trial-related [. .. ]
Job vor 11 Tagen bei Jooble gefunden
EVIDENT Europe GmbH
• Hamburg Hamburg, DE
[. .. ] people at a total of 57 locations worldwide. Evident Europe, headquartered in Hamburg, Germany, employs approximately 770 people in 16 countries. The product portfolio includes a wide [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] range of microscope 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 [. .. ] 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 [. .. ]
Job am 08.04.2026 bei Jooble gefunden
• Berlin Berlin, DE
Clinical Operations Study Country Lead-all genders Bring your passion for AI and data-driven thinking to clinical research that makes a real difference. If you re excited about using data [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] to drive smarter decisions and improve patient lives, we want to meet you About the job Were an R D-[. .. ] 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 ability to create and foster trustful relationships with several internal and and external stakeholders Willingness to travel 10-20 (in-country) Languages : Fluent in German and English Why choose us? Bring the [. .. ]
Job am 08.04.2026 bei Jooble gefunden
Thermo Fisher Scientific
• Region Mittlerer Oberrhein, Württemberg; Regierungsbezirk Karlsruhe; Württemberg Karlsruhe, DE
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
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 [. .. ] research services/ Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/ clinical aspects of project implementation, execution, and closeout Ability to effectively analyse project specific data/ systems to ensure accuracy and efficiency Experience of manage multiple projects with differing priorities at one given time Outstanding communication, teamwork, interpersonal and time management skills Excellent English and German (C1 level) languages Severely disabled applicants with the same aptitude will be given preferential treatment. / Schwerbehinderte Bewerber werden bei gleicher Eignung [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] disposition, review of completeness and accuracy of files, and retrieval of documents for the TMF; prepares site closeout visit reports and associated documentation Attend team meetings as required Participates in systems User Acceptance Testing as required Senior CRA assists with the development and implementation of studyspecific monitoring and reporting procedures, methods, guidelines, and tools; participates in development of participant tracking systems; conducts monitoring assessment visits for the purpose of rescuing a troubled site or performing audit preparation at the direction of [. .. ] process regarding performance of assigned CRAs Other duties as assigned Required Skills and Abilities Require a minimum of four years clinical research experience (e. g. , Clinical Trial Associate, Study Coordinator) or equivalent. Life Science degree or equivalent experience combined with successful completion of a recognized CRA training program is essential Requires a minimum of two years monitoring and site management experience as Clinical Research Associate Pulmonology and Oncology therapeutic expertise Excellent understanding of the clinical research process, clinical trialrelated systems [. .. ]
Job vor 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 [. .. ] for the supervision of pregraduate trainee psychologists and postgraduate trainee psychologists. You actively contribute to the development and improvement of care programs, as 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 [. .. ]
Job am 16.03.2026 bei Jobleads gefunden
Senior Medical Project Manager (m/f/d)
• Hamburg
[. .. ] and patient outcomes around the world. Position Summary Role: Senior Medical Project Manager We are looking for a Senior Medical Project Manager who acts as the execution [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] engine for Mindpeaks clinical and pharmaceutical partnerships. In this role, you bridge the gap between complex biological science and high-speed software delivery. You will take full end-to-end ownership of our most important projects, ensuring they move from kickoff to completion through rigorous planning and superior stakeholder management. Your mission is to ensure that complex project requirements turn into reliable, scalable execution. You are not just a coordinator; you are an operational architect. You build the backbone of our partnership delivery by introducing standardized workflows that make scaling predictable. You dont just follow a processyou improve it. When things go wrong, you dont offer excuses; you find creative solutions to keep the customer happy and the project on [. .. ] in Pathology/ Histology, basic Python skills, or a background in top-tier management consulting. Based in Hamburg with regular on-site presence. What Mindpeak Offers The opportunity to build AI systems that power both clinical cancer diagnostics and data-driven drug development. An open, creative work environment with flat hierarchies and quick decision-making. Be part of an excellent leadership team that invests in continuous development. A centrally located Hamburg office with a beautiful view over the harbor. Application Details Please [. .. ]
Job am 22.02.2026 bei Jobleads gefunden
School Psychologist (2026-27)
• Unterseen, Bern
[. .. ] and what changes or activities may be needed Participates in District level committees Communicates psychological principles and information in a useable and practical manner for broad use [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with schools or systems Participates in activities that promote professional 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 [. .. ] 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 [. .. ]
Job am 20.02.2026 bei Jobleads gefunden
School Psychologist-Part-time (2026-27)
• Unterseen, Bern
[. .. ] and what changes or activities may be needed Participates in District level committees Communicates psychological principles and information in a useable and practical manner for broad use [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] with schools or systems Participates in activities that promote professional 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 [. .. ] 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 [. .. ]
Job am 31.01.2026 bei Jobleads gefunden
Clinical Research Associate III (m/f/d)
• Stein, Baden- Württemberg
[. .. ] too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We [...]
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 [. .. ] 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 priorities Willingness to travel for site visits and meetings Fluency in German and English is required. Proficiency in the language of one of Germanys neighboring countries is an advantage, to support potential cross-border monitoring activities. [. .. ] 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 [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Systems Coordinator pro Jahr?
Als Clinical Systems Coordinator verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Systems Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 15 offene Stellenanzeigen für Clinical Systems Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Systems Coordinator Jobs?
Aktuell suchen 8 Unternehmen nach Bewerbern für Clinical Systems Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Systems Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Systems Coordinator Stellenangebote:
- Fortrea (1 Job)
- Milestone One (1 Job)
- Linical (1 Job)
- EVIDENT Europe GmbH (1 Job)
In welchen Bundesländern werden die meisten Clinical Systems Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Systems Coordinator Jobs werden derzeit in Baden-Württemberg (2 Jobs), Niedersachsen (2 Jobs) und Bayern (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Systems Coordinator Jobs?
Clinical Systems Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
