20 Jobs für Clinical Operations Coordinator
Stellenangebote Clinical Operations 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 [. .. ] understand project scope, budgets, and timelines; manage sitelevel activities and communications to meet project objectives, deliverables, and timelines; and adapt quickly to changing priorities under the oversight of the Clinical Operations Lead or designee. Identify and communicate outofscope activities to the Clinical Operations Lead. Attend, contribute to, and present at study and department meetings. Qualifications Minimum 1 year relevant onsite monitoring experience. Proficiency in German language, written and spoken. BA/ BS degree in a science/ healthcare field, nursing degree, or 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 [. .. ]
Job vor 7 Tagen bei Mindmatch.ai gefunden
Fortrea
Vienna Office: Clinical Project Coordinator for Regulatory Submissions
• AT- 9 Wien
Fortrea is seeking an FSP
Clinical Project
Coordinator in Vienna to support clinical research
operations. This office-based role involves coordinating regulatory submissions, managing documentation, and liaising with teams to ensure [...]
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[...] project success. Candidates should have at least 1 year of experience in a clinical trial environment, familiarity with regulatory processes, and strong skills in Microsoft Office. Fluency in German and English is required. Fortrea [. .. ]
Job vor 3 Tagen bei Jooble gefunden
• Ausland Philippinen, DE
[. .. ] be part of it At Alpha-H, were not just about skincarewere about transforming routines into rituals. As pioneers in acid-based, science-backed skincare, we craft products that deliver [...]
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[...] clinical results at home. With over 27 years of expertise, our award-winning formulas, including the iconic Liquid Gold Exfoliating Treatment, have set new standards in the industry. Alpha-H, a proud member of the Vita Green brand portfolio, is a leading beauty brand headquartered in Australia, dedicated to delivering high-quality products and exceptional customer experiences. As we expand our business, we are searching for a dynamic Influencer and UGC Coordinator to be part of our marketing blueprint. About the Role We are seeking a highly organised, proactive, and detail-oriented Influencer UGC Coordinator to support our growing creator ecosystem. This is a hands-on operational role focused on execution and coordination. You will manage day-to-day outreach, relationship nurturing, campaign execution, and UGC asset delivery, ensuring smooth operations between creators and the Melbourne marketing team. Responsibilities Execute outreach to beauty and skincare influencers/ KOLs (micro to mid-tier) as directed Handle day-to-day communication, follow-ups, and relationship management with existing creators Coordinate gifting, seeding, and paid collaboration deliveries Track deliverables, chase content submissions, and manage approval [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Linical
Clinical Research Associate-Germany
• Deutschland Deutschland, DE
The
Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned sites, [...]
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[...] ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] 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 Manager (COM) will oversee the CRA role. Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and associated documentation; participates in the final selection of investigative sites Conducts site initiation visits; trains [. .. ] 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
• Region München, Bayern; Regierungsbezirk Oberbayern; Bayern München, DE
Clinical Trial Manager/ Local Study Manager Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial [...]
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[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of [. .. ] Qualifications: Bachelors degree or higher degree in Health or Natural Sciences Three years of experience in clinical research. Experience in project management and certain time as field monitor or site coordinator. International experienced preferred. Fluency in German and English. Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Excellent communication, presentation and interpersonal skills We are always excited to connect with great talent. This posting is intended for a possible upcoming opportunity rather than a live role. By [. .. ] 1 clinical research studies at the organization s facilities. Individuals in these roles collaborate closely with the principal investigator, serve as liaisons between research subjects, client teams, investigators, and clinic operations teams, and meticulously plan logistics and resource usage. These roles require tracking study progress in alignment with project milestones, client deliverables, and budget, while ensuring compliance with applicable regulations globally and by region. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may [. .. ]
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 data to [...]
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[...] drive smarter decisions and improve patient lives, we want to meet you About the job Were an R D-driven, [. .. ] 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
KBR
• Landkreis Birkenfeld; Regierungsbezirk Koblenz; Rheinland- Pfalz Baumholder, DE
Title: Special
Operations Performance Dietitian (Baumholder, Germany) Job Posting Description THIS POSITION IS ONSITE THIS POSITION OFFERS RELOCATION Belong. Connect. Grow. with KBR KBR is a company of innovators, [...]
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[...] thinkers, creators, explorers, volunteers, and dreamers; but we all share one goal: to improve the world responsibly and safely. We maintain a highly qualified [. .. ] 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 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 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Business Process
• Hamburg
Homeoffice möglich
[. .. ] technology, or youre looking to apply your relevant experience to a new industry, join our team as we help shape a brighter way forward. Team Assistant (m/w/d) [...]
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[...] Finance Operations Vollzeit Quereinsteigerinnen willkommen. Als Team Assistant Finance Operations übernimmst du eine zentrale Rolle in unserem Germany Value and Risk Advisory (VRA) Team. Business Operations Assistant (m/w/d) Darmstadt Reporting directly to the Workplace Coordinator, the Office Services Assistant will provide exceptional customer service to both internal and external customers. To go above and beyond, making our guests feel welcome and comfortable. Clinical Trials Assistant 1 (m/w/d) Frankfurt, Hesse, Germany We currently offer the exciting opportunity to join the team as Clinical Trials Assistant 1/ CTA I (m/w/d) in fulltime and work officebased in our Germany headquarter in Frankfurt. Occasional homeoffice is possible after onboarding. Administrative Assistant for the [. .. ]
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 [. .. ]
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 [...]
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[...] sites, ensuring site compliance with Good Clinical Practice (GCPs) , applicable regulations, the protocol and study plans; ensuring data integrity through [. .. ] 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 Manager (COM) will oversee the CRA role. Duties and Responsibilities Participates in the identification of potential investigative sites, conducts site qualification visits, collects, and reviews site regulatory documents, and prepares site qualification visit reports and associated documentation; participates in the final selection of investigative sites Conducts site initiation visits; trains [. .. ] 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 [. .. ] management and monitoring of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. You will contribute to the efficiency of clinical research operations by providing advanced support to site management teams and fostering strong relationships with site personnel. What You Will Be Doing Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of siterelated issues. Assisting in the preparation and review of regulatory documents, ensuring all site [. .. ]
Job am 28.03.2026 bei Jobleads gefunden
MSW Program Director Associate/ Professor (Online)
• Steiermark
Führungs-/ Leitungspositionen
[. .. ] Division Division Academic Division Location Location WZ 209 Link to Department Website or Custom Search Page Position Summary, Requirements, and Qualifications Position Summary, Requirements, and Qualifications Overview [...]
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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 [. .. ] pathways and diversify the social work workforce. Engage in teaching, scholarship, and service aligned with the missions of the program, college, and university. Develop and manage program budgets and administrative operations. Teach courses within the online MSW program. Contribute to ongoing curriculum development and program advancement. Minimum Required Qualifications Earned doctorate (Ph D or Ed D) in Social Work or a closely related field Master of Social Work ( MSW ) from a CSWE-accredited program Minimum of two years of post-MSW [. .. ] 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
• 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 [. .. ] pathways and diversify the social work workforce. Engage in teaching, scholarship, and service aligned with the missions of the program, college, and university. Develop and manage program budgets and administrative operations. Teach courses within the online MSW program. Contribute to ongoing curriculum development and program advancement. Minimum Required Qualifications Earned doctorate (Ph D or Ed D) in Social Work or a closely related field Master of Social Work ( MSW ) from a CSWE-accredited program Minimum of two years of post-MSW [. .. ] 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 21.03.2026 bei Jobleads gefunden
Clinic Nurse Manager-Oncology
• Potsdam, Brandenburg
[. .. ] Clinic Nurse Manager Department: Oncology Location: Canton-Potsdam Hospital Hours Per Week: 40 scheduled weekly hours Schedule: 8-hour day shifts, 8-4:30 pm, Monday-Friday SUMMARY Responsible for the
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[...] class=highlight_text>clinical management of assigned PPM Practice (s) servicing patients in and around SLH in St. Lawrence County, New York. Works collaboratively in dyad relationship with Practice Manager (s) /
Coordinator (s) in the supervision and support of clinical care coordinators, LPNs and MAs. Collaborate with key function leaders at SLH such as Director of Quality, Director of Patient Safety, and Director of Patient Experience. Responsible for the management of quality clinical standards for employed and contracted physicians, mid-levels (providers) [. .. ] information on all patients including telephone encounters, reports from outside facilities, preventative services, prescription refill requests and health related concerns. Develops plans as necessary to ensure the successful clinical quality
operations of the facility. Clinical Management Participates in hiring, onboarding, evaluation, and disciplinary activities for all clinical support staff. Works in didactic relationship with Practice Managers and Providers. Oversight of Clinical Care Coordinators and RNs within outpatient practices. Is knowledgeable about all elements of appropriate 1199 SEIU United Healthcare Workers collective [. .. ]
▶ Zur Stellenanzeige
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 track. What Youll Do Driving High-Stakes Projects: Leading pharma partnerships with zero hand-holding and full accountability for results. Scaling Operations: Reducing onboarding times and automating repetitive tasks to move from 25 labs in 2026 to 100+ in 2027. Bridging Science Tech: Translating clinical requirements and pathology results into technical requirements for our engineering teams. Maintaining Excellence: Ensuring high-quality delivery while navigating the high-pressure environment of a fast-growing [. .. ]
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 [. .. ] Perform data review and verification for patient 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
• Hamburg
[. .. ] 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 [...]
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[...] 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 [. .. ]
Job am 13.12.2025 bei Jobleads gefunden
Lead Physiotherapist and Rehab Coordinator Academy (m/f/)
• Leipzig, Sachsen
Führungs-/ Leitungspositionen
Lead Physiotherapist and Rehab
Coordinator Academy (m/f/) Join to apply for the Lead Physiotherapist and Rehab Coordinator Academy (m/f/) role at RB Leipzig Direct message the job poster from [...]
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[...] RB Leipzig Company Description The Lead Physiotherapist Rehabilitation Coordinator provides clinical leadership, operational oversight, and strategic direction to ensure high-quality physiotherapy, rehabilitation, and player availability across the academy. The role leads the physiotherapy team, oversees complex case management, and ensures alignment of assessment, treatment, rehabilitation, documentation, and communication with the academys Return-to-Performance (RTP) model and RB Leipzig medical [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Operations Coordinator pro Jahr?
Als Clinical Operations Coordinator verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Operations Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 20 offene Stellenanzeigen für Clinical Operations Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Operations Coordinator Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Operations Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Operations Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Operations Coordinator Stellenangebote:
- Fortrea (2 Jobs)
- Linical (1 Job)
- KBR (1 Job)
In welchen Bundesländern werden die meisten Clinical Operations Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Operations Coordinator Jobs werden derzeit in Bayern (4 Jobs), Hamburg (3 Jobs) und Baden-Württemberg (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Operations Coordinator Jobs?
Clinical Operations Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
