7 Jobs für Clinical Systems Coordinator
Stellenangebote Clinical Systems Coordinator Jobs
Job vor 2 Tagen bei Jobleads gefunden
• Hamburg
[. .. ] their potential. With us, every single employee puts patients first. Make an impact in advancing Cell Therapy by ensuring the highest standards of quality and compliance. We [...]
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[...] are seeking a Clinical Quality Manager (CQM) (m/f/d) - Cell Therapy to join our Cell Therapy Clinical Operations (CTCO) team. In this role, you will collaborate with the Business Processes, Quality Learning (BPQL) team to provide expert guidance and coaching, enabling the successful delivery of Cell Therapy studies by the Site Management [. .. ] (VQV) , if applicable. Foster an engaging quality culture within CT SMM; develop and implement compliance improvement initiatives. Provide country-level consultation during RIST, inspections, and audits; act as audit coordinator for internal audits and serve as SME during sponsor and investigator site inspections. Act as a key member throughout the inspection process, including consultation for inspection responses. Analyze quality metrics and trends to improve performance and proactively manage issues. Participate in regional CT SMM leadership teams and facilitate quality review [. .. ] experience. At least 4 years of operational and/or quality experience in drug development within a pharmaceutical or clinical setting. Solid understanding of business processes, technology, and clinical study information systems. Proven time management skills and the ability to deliver timely responses and support to internal and external stakeholders. Experience working successfully and collaboratively with both internal teams and external partners. Excellent written and verbal communication skills, with the ability to influence, negotiate, collaborate, solve problems, present effectively, mentor others, and [. .. ]
Job am 06.12.2025 bei Jobleads gefunden
• Berlin
Führungs-/ Leitungspositionen
[. .. ] the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive [...]
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[...] healthcare forward. This Clinical Data Team Lead will be responsible for managing end-to-end delivery of data management services for single/ multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products [. .. ] g. , timelines, financial, process, resource Maintain strong customer relationships Ensure open communications with customer and Quintiles management to manage and meet contractual obligations Service Management Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders Support DM service delivery with comprehensive DM process and technical expertise in executing projects Serve [. .. ] root causes of issues and implement remedial actions Serve as Subject Matter Expert (SME) Provide leadership and expertise in a specific CDM task or technology Maintain internal tracking databases and systems Qualifications Bachelors Degree, or educational equivalent, in health, clinical, biological or mathematical sciences, or related field 5+ years direct Clinical Data Management experience in CRO or pharmaceuticals industry, including 3+ years as a CDM project lead; or equivalent combination of education, training and experience Previous experience and proven competence in [. .. ]
Job am 28.11.2025 bei Jobleads gefunden
• Seibersdorf, Niederösterreich
[. .. ] techniques within a framework of quality assurance. The Dosimetry and Medical Radiation Physics Section (DMRP) is responsible for quality assurance and metrology in radiation medicine. The Section [...]
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[...] works closely with clinical colleagues of the Applied Radiation Biology and Radiotherapy Section and the Nuclear Medicine and Diagnostic Imaging Section. Specifically, DMRP provides technical support in medical physics to ensure the safe and effective applications of nuclear technology in radiotherapy, diagnostic radiology and nuclear medicine. It operates the Dosimetry Laboratory located at the [. .. ] work, and mentors scientific visitors and IAEA DOL fellows in QMS procedures. Role The Quality Manager (Dosimetry Laboratory) is a technical specialist on dosimetry instrumentation, calibration and audit methodologies; a coordinator, developing, maintaining and improving the dosimetry laboratory integrated quality and safety management system; a collaborator, contributing to the DOL R D work; and a mentor for scientific visitors and IAEA fellows in dosimetry calibration and audit techniques, and QMS procedures. Functions/ Key Results Expected Coordinate the development, maintenance and implementation [. .. ] DOL dosimetry auditing and calibration services including quality assurance of data processing and report preparation. Contribute to the DOL R D work, including testing and maintenance of dosimetry and instrumentation systems and developing new auditing procedures. Provide measurement support to coordinated research projects in dosimetry. Act as alternate Radiation Protection, Health and Safety Officer. Mentor scientific visitors and train IAEA fellows in QMS activities. The incumbent may perform his/ her work in areas involving exposure to radioactive materials. Therefore, as an [. .. ]
Job am 27.11.2025 bei Jobleads gefunden
Quality Manager (Dosimetry Laboratory) (P3)
• Seibersdorf, Niederösterreich
[. .. ] techniques within a framework of quality assurance. The Dosimetry and Medical Radiation Physics Section (DMRP) is responsible for quality assurance and metrology in radiation medicine. The Section [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] works closely with clinical colleagues of the Applied Radiation Biology and Radiotherapy Section and the Nuclear Medicine and Diagnostic Imaging Section. Specifically, DMRP provides technical support in medical physics to ensure the safe and effective applications of nuclear technology in radiotherapy, diagnostic radiology and nuclear medicine. It operates the Dosimetry Laboratory located at the [. .. ] work, and mentors scientific visitors and IAEA DOL fellows in QMS procedures. Role The Quality Manager (Dosimetry Laboratory) is: a technical specialist on dosimetry instrumentation, calibration and audit methodologies; a coordinator, developing, maintaining and improving the dosimetry laboratory integrated quality and safety management system; a collaborator, contributing to the DOL R D work; a mentor for scientific visitors and IAEA fellows in dosimetry calibration and audit techniques, and QMS procedures. Functions/ Key Results Expected Coordinate the development, maintenance and implementation of [. .. ] DOL dosimetry auditing and calibration services including quality assurance of data processing and report preparation. Contribute to the DOL R; D work, including testing and maintenance of dosimetry and instrumentation systems and developing new auditing procedures. Provide measurement support to coordinated research projects in dosimetry. Act as alternate Radiation Protection, Health and Safety Officer. Mentor scientific visitors and train IAEA fellows in QMS activities. The incumbent may perform his/ her work in areas involving exposure to radioactive materials. Therefore, as an [. .. ]
Job vor 4 Tagen bei Neuvoo gefunden
IQVIA
• Frankfurt, Hessen
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department is supporting our clients project team in the execution of early clinical trials. Joining our team offers the opportunity to [...]
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[...] work on innovative projects in a dynamic environment. You will support trial preparation, documentation, and coordination, ensuring compliance with regulatory standards and internal processes. [. .. ] role combines operational and administrative responsibilities and requires close collaboration with internal and external stakeholders. We currently offer an exciting opportunity to join the FSP team as global Clinical Trial Coordinator ECT (m/w/d) in full-time and work home-based throughout Germany or Switzerland. RESPONSIBILITIES Coordinate clinical trials in early clinical development for both Sponsor and Study site. Support Clinical Trial Leaders, Clinical Trial Managers, Clinical Research Associates and Principal Investigators in all study-related activities throughout all study phases (preparation, conduct, close-out) . Prepare and manage clinical trial documentation Compilation and collection of submission documents. Maintain trial-specific data and timelines in electronic systems. Communicate effectively with internal and external partners (e. g. , statisticians, data managers, regulatory affairs, investigators) . Organize and monitor study-related activities, meetings, and documentation. Ensure timely preparation of submission documents for authorities and ethics committees. Manage essential documents for Investigator Site File (ISF) and ensure Trial Master File [. .. ]
Job vor 4 Tagen bei Neuvoo gefunden
Astra Zeneca
Clinical Quality Manager (m/f/d) - Cell Therapy
• Hamburg
[. .. ] their potential. With us, every single employee puts patients first. Make an impact in advancing Cell Therapy by ensuring the highest standards of quality and compliance. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are seeking a Clinical Quality Manager (CQM) (m/f/d) - Cell Therapy to join our Cell Therapy Clinical Operations (CTCO) team. In this role, you will collaborate with the Business Processes, Quality Learning (BPQL) team to provide expert guidance and coaching, enabling the successful delivery of Cell Therapy studies by the Site Management [. .. ] (VQV) , if applicable. Foster an engaging quality culture within CT SMM; develop and implement compliance improvement initiatives. Provide country-level consultation during RIST, inspections, and audits; act as audit coordinator for internal audits and serve as SME during sponsor and investigator site inspections. Act as a key member throughout the inspection process, including consultation for inspection responses. Analyze quality metrics and trends to improve performance and proactively manage issues. Participate in regional CT SMM leadership teams and facilitate quality review [. .. ] experience. At least 4 years of operational and/or quality experience in drug development within a pharmaceutical or clinical setting. Solid understanding of business processes, technology, and clinical study information systems. Proven time management skills and the ability to deliver timely responses and support to internal and external stakeholders. Experience working successfully and collaboratively with both internal teams and external partners. Excellent written and verbal communication skills, with the ability to influence, negotiate, collaborate, solve problems, present effectively, mentor others, and [. .. ]
Job vor 14 Tagen bei Neuvoo.com gefunden
Rapid Trials
• Chemnitz
POSITION SUMMARY Rapid Trials is hiring an experienced
Clinical Research
Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. [...]
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[...] This part-time, freelance role is based in Chemnitz, Germany. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, and ensuring compliance with protocol, GDPR, and site SOPs. Location: On-[. .. ] procedures (eg, Fibroscan, biopsy, EGD) Send appointment reminders Organize transportationand follow-up Request/ track medical records Share results with referral sources Coordinate with CRC Complete Sponsor or CRO logs Documentation Systems Enter data into EDC Review and QC data in EDC Compliance Training Complete onboarding requirements: Training on protocol and study-related tools and systems Site Training, including SOPs and workflow Ensure GDPR-compliant data handling, including consent for background checks and data usage EU work authorization and freelancer eligibility (tax [. .. ]
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 7 offene Stellenanzeigen für Clinical Systems Coordinator Jobs.
In welchen Bundesländern werden die meisten Clinical Systems Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Systems Coordinator Jobs werden derzeit in Hamburg (2 Jobs), Hessen (1 Jobs) und Sachsen-Anhalt (1 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Systems Coordinator Jobs?
Clinical Systems Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
