22 Jobs für Clinical Data Coordinator
Stellenangebote Clinical Data 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 [...]
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[...] Anwenderinnen und Anwendern ein breit [. .. ]
Neu Job vor 4 Std. bei Mindmatch.ai gefunden
Syneos Health, Inc.
On-site monitor open to diverse EMEA countries
• 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 [...]
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[...] 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 [. .. ] guidelines. Document activities 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 [. .. ] 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 [...]
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[...] 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 external regulations. Support the preparation and review of study-related documentation. Liaise with internal teams to ensure timely updates and data accuracy. Assist in scheduling meetings, managing email communications, and organizing project files. Monitor timelines and elevate delays or issues to relevant stakeholders. Contribute to continuous improvement of administrative processes. Required Qualifications At least 1 year of work experience in a clinical trial environment. Some experience in clinical research preferred. Regulatory [. .. ]
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 [...]
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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 [. .. ] 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 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. [. .. ]
Job am 19.03.2026 bei Mindmatch.ai gefunden
Milestone One
• AT- 9 Wien
A global site enabling services organization in Austria seeks a Site
Coordinator to support
clinical trial activities. Responsibilities include communication between sponsors and sites, patient enrollment tracking, and
data management. [...]
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[...] The ideal candidate holds a relevant university degree and has at least 2 years of experience as a site coordinator. Fluent English and the local language are required. This position offers the opportunity to grow within a developing company that values its people. J-18808-Ljbffr 84962418 [. .. ]
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 [...]
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[...] 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 [. .. ] 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 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 [. .. ]
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 [...]
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[...] sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations [. .. ] 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 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 [...]
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[...] 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 [. .. ] 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 [. .. ]
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 [...]
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[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Location/ Division Specific Information Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants. Discover Impactful Work: PPD clinical research services mission is to improve health. It starts as an idea to cure. It becomes a [. .. ]
Job am 08.04.2026 bei Jooble gefunden
KBR
Special Operations Performance Dietitian (Baumholder, Germany)
• Landkreis Birkenfeld; Regierungsbezirk Koblenz; Rheinland- Pfalz Baumholder, DE
[. .. ] and Family (POTFF) contract. At KBR we maintain a highly qualified workforce to help care for service people and astronauts-Could this be you? Essential Duties Responsibilities: Performs [...]
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[...] administrative and clinical duties within their scope of practice. Provide nutritional planning, counseling, and documentation that is guided by evidence-based peer reviewed literature. Advise the chain of command on issues pertinent to nutrition and performance nutrition. Work within the scope of practice, which may include ordering labs. Provide individual and group counseling [. .. ] performance nutrition programs for SOF personnel in Garrison, TAd/TDY, and deployed settings. Develop nutritional protocols and guidelines for rehabilitation and performance. Collaborate with the HP program Manager and/or Coordinator for implementation of new protocols and guidelines. Serve as an advisor on dining facility and/or galley nutrition and liaison between food service and command. Assist other regional SOF assets as required by the HP program Manager and/or Coordinator and approved by the chain of command. Attend and participate [. .. ] (e. g. , Smartbase, etc. ) , as directed by HP program manager and/or coordinator and. or required by USSo COM HQ and its POTFF staff. Collect and report all data as requested by the HP program Manager and/or Coordinator and required by USSOCOM HQ and its POTFF staff. Proficiently utilize computers, software, and technologies as required and requested by the HP program Manager and/or Coordinator and required by USSOCOM HQ and its POTFF staff. Required Education/ Experience/ Skills/ [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• 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) [...]
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[...] 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 [. .. ]
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 source data verification and monitoring process, and ensuring site compliance with all Investigational Product (IP) storage, inventory, dispensing, dosing, and disposition requirements. EU CRAs could have a shared role of Regulatory Affairs Officer (RAO) and CRA. The Regulatory department will oversee the RAO role while the Clinical Operations [. .. ] 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 8 Tagen bei Jobleads gefunden
• 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 [...]
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[...] welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Site Management Associate to join [. .. ] activities are compliant with GCP and applicable regulations. Collaborating with crossfunctional teams to facilitate effective communication and support for trial sites throughout the study lifecycle. Tracking site performance metrics, analyzing data, and providing reports to enhance site management efficiency. Participating in training initiatives and mentoring junior staff to support their development in clinical trial management. Your Profile Bachelors degree in a relevant field such as life sciences, healthcare administration, or clinical research. Experience in clinical research, site management, or monitoring, with [. .. ]
Job am 18.04.2026 bei Jobleads gefunden
Clinical Research Nurse
• Berlin
The
Clinical Research Nurse is responsible for providing clinical nursing care for all study participants an accordance with departmental policies and procedures and established standards of nursing care and [...]
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[...] practice in Clinical Trial setting. 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 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 medical devices in the ward Preparing clinical equipment and areas, [. .. ]
Job am 28.03.2026 bei Jobleads gefunden
• 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 [...]
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[...] 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 [. .. ] CSWE accreditation and curriculum design to budget management and staffing. You will drive program growth by managing marketing, recruitment, and field placements while ensuring instructional excellence through continuous evaluation and data analysis. A key focus involves building strategic partnerships with state boards and educational agencies to diversify the social work workforce and strengthen professional pathways. Additionally, you will remain active in the academic community through teaching, scholarship, and committee service aligned with the universitys mission. Essential Duties and Responsibilities Oversee the [. .. ] 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 [. .. ]
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 [...]
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[...] 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 [. .. ] CSWE accreditation and curriculum design to budget management and staffing. You will drive program growth by managing marketing, recruitment, and field placements while ensuring instructional excellence through continuous evaluation and data analysis. A key focus involves building strategic partnerships with state boards and educational agencies to diversify the social work workforce and strengthen professional pathways. Additionally, you will remain active in the academic community through teaching, scholarship, and committee service aligned with the universitys mission. Essential Duties and Responsibilities Oversee the [. .. ] 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 [. .. ]
Job am 16.03.2026 bei Jobleads gefunden
• 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 [...]
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[...] 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 [. .. ] navigating the high-pressure environment of a fast-growing AI startup. Project Governance Execution Lead the end-to-end delivery of high-priority pharmaceutical and clinical projects. Identify red flags (data bottlenecks, regulatory hurdles) weeks in advance and implement mitigation plans. Balance partner feature creep with internal resources, ensuring commitments are met without compromising quality. Stakeholder Architecture Act as a trusted, high-presentability advisor to our Pharma partners. Navigate difficult conversations regarding delays or technical limitations while maintaining excellent long-term [. .. ]
Job am 28.02.2026 bei Jobleads gefunden
Speech Language Pathologist-26-27
• Unterseen, Bern
[. .. ] and strategies. Parent and Caregiver Communication: Communicate regularly with parents and caregivers to provide updates on student progress. Provide resources and guidance for extending speech and language [...]
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[...] support at home. Data Collection and Reporting: Maintain accurate and up-to-date records of student progress and interventions. Generate reports for IEP meetings and collaborate on data-driven decision-making. Professional Development: Stay current with advancements in speech-language pathology and educational practices. Engage in continuous professional learning to enhance therapeutic effectiveness. Additional [. .. ] essential to note that the above description is illustrative and not exhaustive. Qualifications Masters degree in Speech-Language Pathology. State licensure or certification as a Speech-Language Pathologist. Certificate of Clinical Competence in Speech-Language Pathology (CCC-SLP) (preferred) Experience working with students in a school setting is preferred. Commitment to educational equity, inclusivity, and community empowerment. Strong interpersonal, communication, and organizational skills. Benefits FUSD offers a competitive compensation package, along with opportunities for professional development, healthcare coverage, retirement plans, and [. .. ] Age Discrimination Act of 1975, and the Americans with Disabilities Act of 1990. Questions, complaints, or requests for additional information regarding these laws may be forwarded to the designated compliance coordinator (s) : the District Title IX Coordinator, and/or the District 504 Coordinator, both of which can be located on our web page or in person at 1000 South Main Street, Florence, Arizona. Or by phone at (520) 866-3500. #J-18808-Ljbffr 82196173 [. .. ]
Job am 22.02.2026 bei Jobleads gefunden
• Unterseen, Bern
[. .. ] accommodations to facilitate improved student performance in the classroom and at home. Engages in consultation processes with educators and parents, consistent with established models; participates in integration [...]
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[...] of all available data pertaining to students (home, school, community-based) Assists with the development of intervention and accommodation plans; provides jargon free and understandable recommendations to staff and parents Keeps current with literature on crisis prevention and early intervention Develops and maintains a regular building schedule and informs building level staff of variations [. .. ] 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 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
[. .. ] accommodations to facilitate improved student performance in the classroom and at home Engages in consultation processes with educators and parents, consistent with established models; participates in integration [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] of all available data pertaining to students (home, school, communitybased) Assists with the development of intervention and accommodation plans; provides jargonfree and understandable recommendations to staff and parents Keeps current with literature on crisis prevention and early intervention Develops and maintains a regular building schedule and informs building level staff of variations in schedule [. .. ] 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 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 [...]
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[...] 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 [. .. ] 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. Your [. .. ] 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 21.01.2026 bei Jobleads gefunden
Field Data Collection Specialist Surveyor
• Hamburg
Field
Data Collection Specialist Surveyor Join to apply for the Field Data Collection Specialist Surveyor role at TSMG Holding Field Data Collection Specialist Surveyor 9 months ago Be among [...]
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[...] the first 25 applicants Join to apply for the Field Data Collection Specialist Surveyor role at TSMG Holding Company description: Terry Soot Management [. .. ] Management and Manufacturing Industries Outsourcing and Offshoring Consulting Referrals increase your chances of interviewing at TSMG Holding by 2x Sign in to set job alerts for Field Specialist roles. Field Clinical Specialist, Transcatheter Mitral Tricuspid Therapies OEM Field Support Integration Engineer Talent Pool: Field Service Engineer/ Technician (d/f/m) for Diagnostics and Life Sciences in DACH region Field Technical Engineer/ Applikationsspezialist (w/m/d) Elektrophysiologie-Region Hamburg/ Hannover Learning and Development Specialist (all genders) Sales Operations Field Force Coordinator (gn) Field Clinical Specialist Central Lower Saxony-Nurse Biomedical Full time/ Part time Account Leader Energy Resources (w/m/d) Clinical Specialist (m/w/d) VELYS Robotics-Location: Hessen/ NRW Technical Training Program Developer Wind Turbines (d/w/m) Zoiss Engineering Gmb H Senior Compensation Benefits Specialist (all genders) Claims Restructuring [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Data Coordinator pro Jahr?
Als Clinical Data Coordinator verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 22 offene Stellenanzeigen für Clinical Data Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Coordinator Jobs?
Aktuell suchen 8 Unternehmen nach Bewerbern für Clinical Data Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Coordinator Stellenangebote:
- Milestone One (2 Jobs)
- Fortrea (1 Job)
- Linical (1 Job)
- Thermo Fisher Scientific (1 Job)
In welchen Bundesländern werden die meisten Clinical Data Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Coordinator Jobs werden derzeit in Niedersachsen (4 Jobs), Baden-Württemberg (3 Jobs) und Bayern (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Coordinator Jobs?
Clinical Data Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
