16 Jobs für Clinical Trials Coordinator
Stellenangebote Clinical Trials Coordinator Jobs
Job gestern bei Jooble gefunden
Hlx Life Sciences
• Berlin
Were working with a CRO whose seeking a Project Manager with 5+ years of CRO project management experience and a strong understanding of the full
clinical trial lifecycle. Lead clinical [...]
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[...] trials from study start-up through closeout-Manage sponsor relationships and cross-functional project teams-Coordinate activities across Clinical Operations and must have strong experience in Medical Writing, Data Management, and Quality Assurance-Ensure compliance with ICH-GCP, regulatory requirements, and company SOPs-Drive project success through effective communication, planning, and [. .. ]
Job am 06.06.2026 bei Jobleads gefunden
• Zug
Milestone One is looking for a Site
Coordinator in Ciudad de Mxico. The successful candidate will support
clinical trial sites by ensuring compliance with ICH-GCP and protocol requirements. Responsibilities include [...]
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[...] acting as the primary communication link between the Sponsor and site, tracking patient enrollment, and facilitating negotiations for contracts. Candidates must have a degree in Life Science, experience in clinical trials, and effective communication skills. This role offers opportunities for professional growth and development. #J-18808-Ljbffr 94228226 [. .. ]
Job am 05.05.2026 bei Jobleads gefunden
• Zug
Führungs-/ Leitungspositionen
Overview Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what
clinical study sites need and our overall mission is to support sites [...]
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[...] in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific defined timelines and enrollment goals. Responsibilities Act as the main line of communication between the Sponsor or CRO and the site. Ensure response to feasibility questions are provided in due time. Assist in scheduling [. .. ] Science, preferably in pharmacy, nursing or lab analytics. Minimum of 2 years of on-the-job experience in a clinical trial environment, where relevant experience has been gained in clinical trials, clinical terminology, and medical research working in the role of a Study Coordinator or similar function. Upper-intermediate level of English, with the ability to work in a global team environment. Experience in Oncology, Renal, or Cardiology clinical studies is a plus. Ability to work in a fast-paced environment, [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
Job Title: Field
Clinical Research Associate This role supports the Clinical Operations team by overseeing clinical studies, ensuring high-quality human study data collection, and facilitating collaboration between internal study teams, [...]
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[...] contract research organizations, and clinical sites. You will take ownership of site monitoring and study oversight for multiple clinical studies, with a focus [. .. ] experience, including handson support for clinical operations. Experience collaborating with contract research organizations and clinical sites to support study execution. Experience facilitating training of site and vendor personnel for clinical trials. Proven track record in tracking and managing regulatory documentation for clinical studies. Experience in analyzing and reconciling clinical study data and generating operational or invoicing reports. Demonstrated ability to monitor clinical sites and ensure adherence to study protocols and regulatory standards. Strong attention to detail to ensure compliance with study [. .. ] guidelines relevant to clinical research. Willingness and ability to travel when required for study needs, while supporting primarily virtual monitoring activities. Additional Skills Qualifications Experience similar to a clinical research coordinator, particularly in invoicing, data tracking, and trial closeout activities. Experience working with or for a contract research organization or in a sponsor role supporting clinical studies. Experience in clinical operations, clinical trial execution, or field clinical roles such as Field Clinical Research Manager or Field Clinical Specialist. Exposure to health [. .. ]
Job vor 12 Tagen bei Jobleads gefunden
• Luzern
Führungs-/ Leitungspositionen
[. .. ] health. If youre looking to join a successful, global company with real career opportunities, wed love to meet you. About the Role We are seeking an experienced [...]
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[...] and proactive Global Clinical Operations Lead (f/m/d) to manage and oversee clinical trials/ clinical studies/ clinical investigations from initiation to close-out. This role will work closely with GC crossfunctional project teams, investigators, and Contract Research Organizations (CRO) to ensure that studies are conducted in compliance with applicable regulatory requirements, Good Clinical Practice (GCP) , and applicable institutional policies. Key responsibilities include ensuring [. .. ] management systems. Excellent command of English is required; knowledge of additional languages will be considered an asset. Willingness to travel internationally as required. Preferred Qualifications Certification as a Clinical Research Coordinator recognized in the US or Europe. Proficiency in class III dental medical devices. Experience with clinical trials preparation, monitoring, tracking and reporting at CRO. Familiarity with electronic medical records (EMR) and patient data privacy regulations (e. g. , EU GDPR, U. S. HIPAA) . Success Metrics Ontime and compliant delivery [. .. ]
Job am 21.05.2026 bei Jobleads gefunden
• Wien
Absolventen, Einsteiger, Trainees
Work-Life-Balance
Study start up CRA, Austria 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 [...]
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[...] welcome you to join us on our mission to shape the future of clinical development. As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key Responsibilities Include Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring [. .. ] skills. Required Qualifications And Experience Bachelors degree in a scientific or healthcare-related field. Minimum of 1 year of experience in the clinical research field (e. g. , as Study Coordinator or similar) . In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60) . Fluency in German and English language. What [. .. ]
Job am 10.05.2026 bei Jobleads gefunden
• Hamburg
Homeoffice möglich
[. .. ] 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 [...]
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[...] 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 Climate [. .. ]
Neu Job vor 3 Std. 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 [...]
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[...] work with the preparation and documentation of clinical research projects in different therapeutic areas. We currently offer the exciting opportunity to join the team as Clinical Trials Assistant 2 (m/w/d) in full-time and work in a combination of office and [. .. ] or pharmaceutical field or office management. At least 2 years of experience as Clinical Trials Assistant or in another administrative role in clinical research, e. g. as Project Assistant, Study Coordinator, Study Nurse. Excellent knowledge of applicable clinical research regulatory requirements, i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Fluent languages skills in German on at least C1 level and good command of English. Computer skills including working knowledge of Microsoft Word, Excel and Power [. .. ]
Job vor 10 Tagen 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 an exciting opportunity to join the team as Experienced Clinical Trial Coordinator (m/w/d) to work in home-office anywhere in Germany. Your responsibilities might include: 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 [. .. ]
Job am 07.06.2026 bei Neuvoo gefunden
Subject Well Inc.
• München- Flughafen, Bayern
Freiberuflich
Accelerate patient enrollment in
clinical trials with Subject Well/ Clariness, helping patients gain access to life-changing medications. We support biopharmaceutical companies and CROs in completing clinical trials faster so innovative [...]
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[...] treatments can reach patients sooner. If you enjoy helping people and have strong communication skills, join our virtual team and contribute to meaningful medical research. We are currently seeking a Freelance Study Coordinator to support our team in handling unscripted patient calls related to oncology clinical trials. If you have a medical background, excellent communication skills, and experience in oncology or clinical research, this could be a great fit. Tasks About the role As an Onco-Companion Patient Recruitment, you will serve as [. .. ]
Job am 25.05.2026 bei Neuvoo gefunden
Sanofi
Junior Discovery Pharmacokinetics Outsourcing Partner VIE Contract
• Frankfurt, Hessen
Absolventen, Einsteiger, Trainees
Work-Life-Balance
[. .. ] are submitted in English will be considered. Please make sure to apply with your personal email address. About the job About Sanofi Main responsibilities: Study Management: Serve [...]
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[...] as the study coordinator for the outsourcing and operationalization of preclinical PK and TK activities, ensuring scientific integrity, adherence to timelines, quality deliverables, and budget compliance. Central Point of Contact: Act as liaison for all discovery PK/ TK-related activities, both internal and external providing the team with high-quality data to support informed [. .. ] vendor activities. Hands-on experience with complex data sets and proficiency with Certaras Phoenix and D360 software solutions would be an asset. Soft and technical skills: Solid understanding of non-clinical in vivo PK study design, LC/ MS-and LBA-based bioanalysis, and PK/ TK evaluation. Working knowledge of Gx P regulations and the ability to identify and troubleshoot issues arising from external vendor study activities. Strong communication skills with the ability to collaborate effectively across multiple teams and stakeholder groups, with [. .. ] Work Abroad Program, i Move, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our i Move Work Abroad Program is a unique opportunity to make a difference through your work. #LI-EUR Pursue, discover Better is out there. Better medications, better [. .. ]
Job am 17.05.2026 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 [...]
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[...] 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 14.04.2026 bei Neuvoo gefunden
Parexel
Clinical Research Coordinator
• Berlin
When our values align, theres no limit to what we can achieve. The
Clinical Research
Coordinator is accountable for the planning, preparation, and execution of clinical
trials [...]
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[...] in conjunction with the Team Leader, Project Manager, and Investigator. This role ensures that clinical studies are conducted according to the study protocol, ICH GCP guidelines, and unit SOPs. The coordinator assists in the conduct of Phase I-III studies across all therapeutic areas, ensuring studies are prepared to the [. .. ]
Job am 15.02.2026 bei Neuvoo gefunden
Thermo Fisher Scientific
Clinical Trial Coordinator II (m/f/d)
• 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 [...]
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[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the [. .. ] also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our dedicated, forward-thinking and upbeat teams. Position Overview: As a Clinical Trial Coordinator, you will provide administrative and technical support to the Project Team. You will support audit readiness by ensuring files are reviewed on schedule detailed in the organizations WPD and department guidance document. Essential Functions: According to the specific role (Central or Local) , coordinates, oversees and completes functions on assigned [. .. ]
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 [...]
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[...] 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 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 [...]
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[...] 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 [. .. ]
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 16 offene Stellenanzeigen für Clinical Trials Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trials Coordinator Jobs?
Aktuell suchen 9 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:
- IQVIA (2 Jobs)
- Georgetown University in Qatar (2 Jobs)
- Hlx Life Sciences (1 Job)
- Subject Well Inc. (1 Job)
- Sanofi (1 Job)
- Parexel (1 Job)
In welchen Bundesländern werden die meisten Clinical Trials Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Coordinator Jobs werden derzeit in Sachsen-Anhalt (3 Jobs), Hessen (3 Jobs) und Sachsen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Coordinator Jobs?
Clinical Trials Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
