25 Jobs für Clinical Trials Coordinator
Stellenangebote Clinical Trials 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 activities [. .. ] 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 activities [. .. ] 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 activities [. .. ] 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 activities [. .. ] 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 activities [. .. ] 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 activities [. .. ] 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 vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
• Karlsruhe
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ]
Job am 16.01.2026 bei Jooble gefunden
Milestone One
Regional Clinical Operations Manager
• 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 stronger [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 to be assigned. Key Responsibilities Take [. .. ]
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 stronger [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 research projects within the assigned region. [. .. ]
Job am 14.01.2026 bei Jooble gefunden
ICON
Site Engagement Liaison
• Homeoffice
Work-Life-Balance
ICON plc is a world-leading healthcare intelligence and
clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] our mission to shape the future of clinical development. As a Site Engagement Liaison (SEL) will be responsible for developing relationships with clinical trial investigators and research site staff to facilitate recruitment of subjects in pharmaceutical industry clinical trials. You will be partnering with one of the worlds premier Biopharmaceutical companies. Working across a vast portfolio of medicines and vaccines this company has, over centuries created a strong heritage of delivering innovative treatments and preventive medicines globally. What you will be doing: Work with clinical research associates (CRAs) and [. .. ] are: Experience in site management, start-up activities to site activation, and close-out activities Exposure to the clinical research environment as a SEL, medical science liaison (MSL) , study coordinator, Senior CRA or experience in a CRO Demonstrated knowledge of quality and regulatory requirements in applicable countries Excellent communication skills in German and English Ability to travel What ICON can offer you: Our success depends on the quality of our people. Thats why weve made it a priority to build [. .. ]
Job am 14.01.2026 bei Jooble gefunden
Biocair
• Hamburg
The role of the Customer Care
Coordinator (Logistics Coordinator) is to deliver the highest quality service in our industry by meticulously overseeing every aspect of the shipment process, ensuring [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] that all shipments are managed with the utmost efficiency, safety, and cost-effectiveness while maintaining clear communication with clients, addressing their concerns promptly, and consistently striving to exceed [. .. ] orders and enquiries and ensure that customer interactions are handled in a pro-active and professional manner at all times. Manage the end to end shipment process for research samples, clinical trials medicines and other pharmaceutical and healthcare related products, on a worldwide basis Ensure correct and timely completion of all after shipment tasks Develop and maintain a close relationship with existing and potential clients by understanding needs, providing high levels of accurate and timely communication, ensuring complete satisfaction with the service [. .. ]
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 study sites independently, from start-up to closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRA IIIs are expected to guide junior team members Handson experience [. .. ] 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 sites independently, from start-up to closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRAs are expected to guide junior team members Hands-on experience [. .. ] 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 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. Key Responsibilities Take endtoend operational responsibility [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
• 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 sites independently, from start-up to closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRA IIIs are expected to guide junior team members Handson experience [. .. ] 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 19.12.2025 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 [. .. ] CTCO Process Owners to ensure all established SMM processes align with global quality standards. Leading or contributing to quality-related initiatives and continuous improvement programs that enhance compliance within CTCO trials and processes. Collaborating actively with the Director, Cell Therapy Quality Management to strengthen quality culture and compliance across the organization. Typical Responsibilities Assess training compliance of local SMM teams as part of quality oversight activities; deliver onboarding and ad hoc training on quality and compliance topics. Share global process updates [. .. ] (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 gestern bei Neuvoo gefunden
IQVIA
• Frankfurt, Hessen
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department issupporting our clients project team in the execution of clinical
trials. Joining the team provides the opportunity to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] work with the preparation and documentation of clinical research projects in different therapeutic areas in Germany or the DACH region. You will be involved in data management, creation of study related documents and correspondence with internal departments, research sites and our client to ensure a complete and accurate Trial Master File delivery. We currently offer the exciting opportunity to join the team as Experienced Clinical Trial Coordinator (m/w/d) in full-time and work in home-office throughout Germany. RESPONSIBILITIES Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e. g. , Trial Master File (TMF) ) that track site compliance and performance within [. .. ]
Job vor 2 Tagen bei Neuvoo gefunden
Georgetown University in Qatar
Research Data Coordinator I
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job Overview [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] The Research Data Coordinator I position is responsible for data management for phase I, II, and III oncology clinical trials conducted within the Clinical Research Management Office (CRMO) of the Lombardi Comprehensive Cancer Center (LCCC) . Additional duties include, but are not limited to: Supports all aspects of clinical research data management for clinical trials conducted in the LCCC Clinical Research Management Office (CRMO) , including collection of data from [. .. ]
Job vor 3 Tagen bei Neuvoo gefunden
IQVIA
• Frankfurt, Hessen
Homeoffice möglich
The IQVIA sponsor-dedicated
Clinical Functional Service Partnerships (Clinical FSP) department is supporting our clients project team in the execution of early clinical
trials. Joining our team offers the [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] opportunity to work on innovative projects in a dynamic environment. You will support trial preparation, documentation, and coordination, ensuring compliance with regulatory standards and internal processes. This role combines operational and administrative responsibilities and requires close collaboration with internal and external stakeholders. We currently offer an exciting opportunity to join the FSP team as global Clinical Trial Coordinator ECT (m/w/d) in full-time and work home-based throughout Germany. RESPONSIBILITIES Coordinate clinical trials in early clinical development for both Sponsor and Study site. Support Clinical Trial Leaders, Clinical Trial Managers, Clinical Research Associates and Principal Investigators in all study-related activities throughout all study phases (preparation, [. .. ]
Job vor 6 Tagen bei Neuvoo gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d) - Germany
• Karlsruhe, Baden- Württemberg
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ]
Job am 23.01.2026 bei Neuvoo gefunden
Georgetown University in Qatar
Clinical Research Nurse II
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Overview Serves as Clinical Research Nurse 2 for the Cellular Therapy Program oncology clinical trials conducted in the Lombardi Clinical Trials Office of the Lombardi Comprehensive Cancer Center at Georgetown University. Incumbent duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Collaborate with investigators and more senior study team members by participating in recruitment and [. .. ] trials. Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials with Clinical Research Coordinators. Collaborate with Data Coordinator (s) to assure the documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. Document and report serious adverse events per protocol and institutional policy. Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors. Act [. .. ]
Job am 16.01.2026 bei Neuvoo gefunden
Milestone One
Regional Clinical Operations Manager
• Munich, Bavaria
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 to be assigned. Key Responsibilities Take [. .. ]
Job am 16.01.2026 bei Neuvoo gefunden
PSI
Regional Clinical Operations Manager.
• Munich, Bavaria
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 to be assigned. Key Responsibilities Take [. .. ]
Job am 14.01.2026 bei Neuvoo gefunden
Georgetown University in Qatar
Clinical Research Nurse 1
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Overview Serves as Clinical Research Nurse 1 for phase I, II and III oncology clinical trials conducted in the Lombardi Clinical Trials Office (Lombardi CTO) at Lombardi Comprehensive Cancer Center. Incumbent duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Collaborate with investigators and more senior study team members by participating in recruitment and selection of [. .. ] chart, in compliance with protocol and sponsor requirements. Conduct follow-up with study participants in accordance with established standards and protocols. Provide clinical and administrative nursing support to Clinical Research Coordinator and Clinical Research Nurse positions. Ensure site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities. Coordinate collection of research specimens per protocol requirements with Clinical Research Coordinators. Provide patient education about clinical trial participation, treatment, potential [. .. ]
Job am 07.01.2026 bei Neuvoo gefunden
MRI Network
Clinical Research Coordinator
• Östlicher Neubäuer Forst, Bayern
Clinical Research
Coordinator (Onsite) Dallas, TX Ready to make an impact in medical research? This Clinical Research Coordinator role offers the chance to play a vital part in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] advancing patient care through high-quality, hospital-based clinical trials. The position involves coordinating study activities, collecting data, ensuring compliance, and collaborating with physicians, sponsors, and research teams to keep studies on track and accurate. Company Summary This organization leads with purposeconducting ethical, precise, and innovative clinical research that improves lives. The team is dedicated to advancing healthcare by fostering [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Trials Coordinator pro Jahr?
Als Clinical Trials Coordinator verdient man zwischen EUR 45.000,- bis EUR 65.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trials Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 25 offene Stellenanzeigen für Clinical Trials Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Coordinator Jobs?
Aktuell suchen 10 Unternehmen nach Bewerbern für Clinical Trials Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trials Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trials Coordinator Stellenangebote:
- Abb Vie (6 Jobs)
- Milestone One (3 Jobs)
- Georgetown University in Qatar (3 Jobs)
- Thermo Fisher Scientific (2 Jobs)
- IQVIA (2 Jobs)
- ICON (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Coordinator Jobs werden derzeit in Baden-Württemberg (4 Jobs), Bayern (3 Jobs) und Rheinland-Pfalz (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Coordinator Jobs?
Clinical Trials Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
