34 Jobs für Clinical Operations Coordinator
Stellenangebote Clinical Operations Coordinator Jobs
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening [. .. ] with stakeholders. Maintains and completes own expense reports as per local and applicable guidelines. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Qualifications Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Current knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, [. .. ]
Job am 23.01.2026 bei Jooble gefunden
University of Maryland Global Campus
• Homeoffice
Werkstudenten
Student Wellness Basic Needs
Coordinator (Non-
Clinical) Office of Student Affairs Part Time (19hrs a week) , Non-Exempt Contingent 1 Remote UMGC seeks a compassionate, solution-focused professional to serve [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Coordinator of Wellness Basic Needs within Global Student Support Services. This role supports a global population of adult learners by reducing barriers related to wellness, [. .. ] Design and deliver virtual workshops, campaigns, and outreach initiatives that promote proactive wellness, resilience, and awareness among students, faculty, and staff. Support food insecurity and basic needs initiatives, including pantry operations and institutional giving programs. Build and maintain partnerships with Financial Aid, Global Military Operations, Title IX, Accessibility Services, the Behavioral Intervention Team, and other student support units. Collect and analyze student feedback and service data to drive continuous improvement and surface actionable trends. Support department-wide initiatives advancing equity, belonging, [. .. ]
Job am 20.01.2026 bei Jooble gefunden
KBR
Special Operations Physical Therapist (Baumholder, Germany)
• Stuttgart
Title: Special
Operations Physical Therapist (Baumholder, Germany) THIS POSITION OFFERS RELOCATION. Belong. Connect. Grow. with KBR KBR is a company of innovators, thinkers, creators, explorers, volunteers, and dreamers; but [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] we all share one goal: to improve the world responsibly and safely. We maintain a highly qualified workforce to help care for service people [. .. ] following services in support of POTFFs HP program for SOF personnel, with the priority on SOF Operators and Direct Combat Support personnel: Provide neuro-musculoskeletal injury care, utilizing approved supplemental clinical privileges including the ordering of images, laboratory tests, pharmaceuticals, dry needling, acupuncture, joint injections and aspirations, and referrals to specialty providers. If directed by HP Program Manager and/or Coordinator, directly supervise the PT Tech, PT Assistant, and/or Certified Athletic Trainer (ATC) within their scope of practice. Participate in periodic meetings with HP and POTFF for reasons such as, but not limited to, reviewing care provided to patients. Identify opportunities for improvement. Serve as an advisor to the HP [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
• München
Milestone One is a Site Enabling 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 As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. This is a regional role, with the region [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
Area Operations Manager-Clinical
• München
Milestone One is a Site Enabling 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. As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, leading site operations, managing coordinator teams, and ensuring that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a hands-on leader with deep knowledge of clinical trial operations who can proactively identify and resolve day-to-day challenges in a dynamic international environment. Take end-to-end operational responsibility for clinical [. .. ]
Job am 21.01.2026 bei Jooble gefunden
Doctolib GmbH
• Berlin
[. .. ] the Netherlands, we re reinventing how care is delivered through a new generation of AI-powered technologies and services. Our Operating System supports health professionals in all their [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities, from clinical, financial, to admin and care cooperation. Our Health Companion helps people prevent health problems, detect risks earlier, access care faster, and better follow treatments. Today, over 90 million people use Doctolib to manage their health and find care, while 420K health professionals use Doctolib to focus on what matters most: caring for patients. Your tasks What you ll do We are looking for a Talent Acquisition Coordinator to join the Tech Product Recruiting Team in our Berlin office. As a Coordinator, you ll focus on three essential areas: delivering exceptional candidate experience, mastering complex tech product interview scheduling, and continuously improving our interview processes. In this role, you ll gain comprehensive insight into recruitment while applying your [. .. ] s shoes and a genuine passion for finding solutions that work best for everyone A curious, problem-solving mindset with a willingness to learn and dig deeper to understand how operations and processes work Fluency in English with strong verbal and written communication skills, allowing you to adapt your expression to different audiences and situations Now, it would be fantastic if you: Speak German, French or Italian We offer Job details Internship-6 months Full-time Workplace: Berlin Start date: February [. .. ]
Job am 15.01.2026 bei Jooble gefunden
Senior Site Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model
• München
Führungs-/ Leitungspositionen
Senior Site Contracts Lead (Multiple location: Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem [. .. ] relationships with customer and internal project teams. Escalates deviations to senior management and is equipped to resolve issues with Quality Assurance. Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues. Identifies best practices, investigates root causes of fundamental issues and problems for projects and recommends solutions. Trains and mentors less experienced staff members on department Standard Operating Procedures (SOPs) , processes, tools and templates and ensures quality of teamwork products. May [. .. ] . BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/ pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Proficient in MS Office (Word, Excel and Power Point) , MS Project, outlook and Internet. Ability to handle multiple tasks to meet deadlines, delivering high quality work in [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Frankfurt am Main
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] e. 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 [. .. ]
Job vor 8 Tagen 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 [. .. ] 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 vor 11 Tagen bei Jobleads gefunden
• Hechingen, 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 study [. .. ] 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 vor 12 Tagen bei Jobleads gefunden
Project Manager in Regulatory Affairs (f/m/D)
• Kaiserslautern, Rheinland- Pfalz
Work-Life-Balance
[. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Reporting to project coordinator, partners and funding agencies. Your profile Master s degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell therapies is considered beneficial. Experience in regulatory frameworks relevant to biotechnology and biomedical products (e. g. EU GMO regulation, medical device regulation (MDR) , ATMPs) is highly desirable. Strong analytical skills and attention to detail. Clear writing and strong communication skills in German and English. Project management [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 21.01.2026 bei Jobleads gefunden
Data Team Lead/Senior Data Team Lead (m/w/D)
• 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] e. 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 [. .. ]
Job am 20.01.2026 bei Jobleads gefunden
• Saarbrücken, Saarland
Work-Life-Balance
[. .. ] network. Conceptualization of the outreach action plan (website, online platform, workshops) in cooperation with scientists in Material Vital Hub and communication experts at INM and partner institutions. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Reporting to project coordinator, partners and funding agencies. Your profile Masters degree in Regulatory Affairs and at least 2 years of related work experience. Alternatively, university degree in natural, engineering or life sciences and several years experience in regulatory science or regulatory affairs. A Ph D in biomedical materials, microbiology, or experience in clinical translation of cell therapies is considered beneficial. Experience in regulatory frameworks relevant to biotechnology and biomedical products (e. g. EU GMO regulation, medical device regulation (MDR) , ATMPs) is highly desirable. Strong analytical skills and attention to detail. Clear writing and strong communication skills in German and English. Project management [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Regional Clinical Operations Manager
• München, Bayern
Milestone One is a Site Enabling 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 As Milestone One continues its global expansion, we are seeking an experienced Operations Manager to join our international team. This newly created role is critical to ensuring operational excellence across our regional activities and supporting the scalable, high-quality delivery of clinical research projects worldwide. The Operations Manager will take full operational ownership of assigned regions, lead site operations, manage coordinator teams, and ensure that clinical trials are executed efficiently, compliantly, and without disruption. This role requires a handson leader with deep knowledge of clinical trial operations who can proactively identify and resolve daytoday challenges in a dynamic international environment. This is a regional role, with the region to be assigned. [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Clinical Research Associate III
• Berlin
[. .. ] counts, 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. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We are hiring Clinical Research Associate III (m/f/d) Location: EMEA (Flexible) Your strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials on human subjects (e. g. , ISO 14155, GCP, MDR, EU, FDA) Ability to manage 1015 study [. .. ] 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 purposedriven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure to [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Senior Site Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] January 14, 2026 Location: Munich, Germany Job ID: 25104919-OTHLOC-3530-2DR Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] maintains document status reports, and updates department tools/ systems and team members on a regular basis; ensures appropriate documentation is maintained. Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues. Manages site and study level discussions with internal and sponsor team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites. Identifies best practices, investigates root causes of fundamental issues and [. .. ] Qualifications BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/ pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Strong presentation, documentation and interpersonal skills. Proficient in MS Office (Word, Excel and Power Point) , MS Project, Outlook and Internet. Ability to handle multiple tasks to meet [. .. ]
Job am 18.01.2026 bei Jobleads gefunden
Senior Site Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model
• München, Bayern
Führungs-/ Leitungspositionen
[. .. ] Contracts Lead (Multiple location: Poland, Spain, France, Hungary, Serbia) - FSP Model Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] maintains document status reports, and updates department tools/ systems and team members on a regular basis; ensures appropriate documentation is maintained. Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues. Manages site and study level discussions with internal and sponsor team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites. Identifies best practices, investigates root causes of fundamental issues and [. .. ] Qualifications BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/ pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Strong presentation, documentation and interpersonal skills. Proficient in MS Office (Word, Excel and Power Point) , MS Project, outlook and Internet. Ability to handle multiple tasks to meet [. .. ]
Job am 19.12.2025 bei Jobleads gefunden
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 and Monitoring (SMM) organization. The CQM (m/f/d) is responsible for developing, tracking, and analyzing [. .. ] (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 [. .. ]
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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
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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 34 offene Stellenanzeigen für Clinical Operations Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Operations Coordinator Jobs?
Aktuell suchen 9 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:
- Abb Vie (6 Jobs)
- Milestone One (3 Jobs)
- IQVIA (2 Jobs)
- Georgetown University in Qatar (2 Jobs)
- University of Maryland Global Campus (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 (6 Jobs), Rheinland-Pfalz (5 Jobs) und Berlin (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Operations Coordinator Jobs?
Clinical Operations Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
