13 Jobs für Clinical Trial Coordinator
Stellenangebote Clinical Trial Coordinator Jobs
Job vor 7 Tagen bei Neuvoo gefunden
IQVIA
• Frankfurt, Hessen
Homeoffice möglich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team as global Clinical Trial Coordinator ECT (m/w/d) in full-time and work home-based throughout Germany, Austria and Switzerland. 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 [. .. ]
Job vor 5 Tagen bei StepStone gefunden
Milteny GmbH
• Bergisch Gladbach
Homeoffice möglich
Miltenyi Biomedicine is a biopharmaceutical company committed to advancing personalized cell and gene therapies. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for
clinical professionals [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and patients worldwide with the aim to improve and extend patients lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. Join our highly professional team in bringing new medicines to market and ensuring the safety of our pharmacological developments at all stages. As a Clinical Trial Assistant, you will be supporting the Clinical Trial Manager in all aspects that are required to keep the quality and timeliness of study data and communication on a high level: You support the distribution and tracking of critical clinical documents and information, e. g. essential documents, study supplies, budgets, manuals, [. .. ] in internal team meetings, taking minutes and providing status updates. You have already gained experience in clinical research as a clinical trial associate, clinical research associate and/or clinical study coordinator in the pharmaceutical/ biotech industry and/or you are a holder of an academic degree in life sciences, natural sciences, or healthcare. Attention to detail comes naturally to you as well as being highly organized. You are are used to prioritize multiple tasks, to take initiative, to work independently and [. .. ]
Job vor 2 Tagen bei Jobleads gefunden
• München, Bayern
[. .. ] Summary Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and engage in clinical trial management on a daytoday level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the companys success. Responsibilities Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile and maintain [. .. ]
Job am 25.11.2025 bei Jobleads gefunden
• Wien
Are you ready to make an impact in
clinical research while leveraging your administrative expertise Join our dynamic FSP team in Vienna as a and help shape the future of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] clinical development at Fortrea. Why this role matters : You will play a key role in supporting clinical trial operations ensuring smooth coordination and documentation and contributing to the success of our client research programs. Your attention to detail and communication skills will help drive excellence in trial execution. What youll do : Provide administrative support for clinical trial activities including documentation tracking and reporting. Collaborate with cross-functional [. .. ] 1 year of professional experience in a company setting Experience or exposure to clinical research is preferred. Administrative experience in clinical settings preferred for instance if previous experience as Study Coordinator. Excellent German language skills (C1 or native) and strong English skills both verbal and written. Outstanding communication and organizational skills. High affinity for electronic systems and digital tools. Positive attitude and willingness to follow best practices and team recommendations. Full-time availability and willingness to work office-based in client [. .. ]
Job am 21.11.2025 bei Jobleads gefunden
Clinical Project Coordinator
• München, Bayern
[. .. ] Summary Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing German team [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the companys success. Responsibilities Work closely with the Project Clinical Trial Manager for timely delivery of recurrent tasks consistently with a high degree of accuracy; Compile [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
[. .. ] review, approval, and implementation of medical and commercial materials. You will be product or project business lead for global CMRP at Takeda CMRP Meeting Chair-pausing to communicate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] comments to coordinator, diffusing team disputes, serving as a dependable negotiator, keeping team focus on our ultimate stakeholders which are the patients who trust us to do the right thing, and overseeing escalation steps if MLR cannot come to alignment or if there is new data or campaigns that require senior level management input or alignment. Strategic business partner from clinical trial development through the marketing maintenance phase of a product lifecycle Subject matter expert on EFPIA, IFPMA, and FDA code/ regs, guidance, industry standards, complaints/ violations, and innovative promotional platforms Act as a strategic partner spanning clinical trial development through the marketing and maintenance phases of the product lifecycle. Regulatory Subject [. .. ]
Job am 26.09.2025 bei Jobleads gefunden
• Essen, Nordrhein- Westfalen
Overview Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/ deficiencies and corrective/ preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/ drug accountability and inventory; Verification and review of adverse [. .. ]
Job am 20.09.2025 bei Jobleads gefunden
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
Clinical Research Associate (Home-Based) - Clinical Research
Coordinator Experience Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage [. .. ] deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/ deficiencies and corrective/ preventive actions to bring a site back into compliance and mitigate risks moving forward; Verification that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/ drug accountability and inventory; Verification and review of adverse [. .. ]
Job am 15.09.2025 bei Jobleads gefunden
• München, Bayern
Job Summary Medpace is currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience for a full-time, office-based Associate
Clinical Trial Manager (a CTM) to join our Clinical Trial Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team. The a CTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in [. .. ] and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM) . Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Manage and perform quality control of our [. .. ]
Job am 11.09.2025 bei Jobleads gefunden
• München, Bayern
Job Summary Medpace is currently seeking candidates with Ph Ds and/or Post-Doctoral Research experience for a full-time, office-based Associate
Clinical Trial Manager (a CTM) to join our Clinical Trial Management [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team. The a CTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in [. .. ] and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM) . Responsibilities Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy Compile and maintain project-specific status reports within the clinical trial management system Interact with the internal project team, Sponsor, study sites, and third-party vendors Manage and perform quality control of our [. .. ]
Job vor 7 Tagen bei Neuvoo.com gefunden
Rapid Trials
Clinical Research Coordinator (Part-time, On-site, Independent Contractor)
• Chemnitz
POSITION SUMMARY Rapid Trials is hiring an experienced
Clinical Research
Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical
trial. This [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] part-time, freelance role is based in Chemnitz, Germany. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, and ensuring compliance with protocol, GDPR, and site SOPs. Location: On-site, Chemnitz, Germany Contract Type: Independent Contractor/ Freelance Duration: 3 months Hours: 8 hours/ day, Monday-Friday Total [. .. ]
Job vor 9 Tagen bei Neuvoo gefunden
Sanofi
Clinical Operations Study Country Lead I-all genders
• Frankfurt, Hessen
Führungs-/ Leitungspositionen
Clinical Operations Study Country Lead I (COSCL) - all genders Join the engine of Sanofis mission where deep immunoscience meets bold, AI-powered research. In the Clinical Study Unit, youll [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] drive breakthroughs that could turn the impossible into possible for millions. About Sanofi: Were an R D-driven, AI-powered biopharma [. .. ] Collaborate with Vendor Functional Line Managers to drive quality and study KPIs Coordinate with Medical Advisors, Site Engagement Leads, and other key stakeholders Establish productive partnerships with Medical Affairs for trial conduct activities Quality Compliance Assurance Ensure data quality, patient safety, and compliance with study metrics Oversee appropriate data collection and query resolution processes Collaborate on audit and inspection activities Maintain system readiness (PAI, TMF, CTMS) and ensure CRA training compliance Required Qualifications and Experience: Bachelors or Masters degree (or higher) in medicine, pharmacy, biology, biochemistry, or related natural science Mandatory: Clinical Research experience Preferred: Project management experience combined with field monitor or site-coordinator background Solid knowledge of clinical development processes and relevant therapeutic areas Core Competencies: Strong project management skills with proven ability to manage complex timelines Excellent problem-solving and risk-management capabilities in clinical study environments Proficiency in data analytics and digital tools, platforms, and systems Change management skills with adaptability [. .. ]
Job am 20.10.2025 bei Neuvoo.com gefunden
Medpace
Experienced Regulatory Submissions (Study Start Up) Coordinator
• Munich
Medpace Overview Medpace is a full-service
clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5, 000 people across 40+ countries. Job Summary As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team office-based in Munich, and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators, you will gain valuable hands-on experience to enable you to develop a career in clinical research. Responsibilities Prepare, review, and file initial clinical trial applications to regulatory authorities and Ethics committees in Germany, Austria and Switzerland; Prepare and submit responses to queries and amendments to clinical trial applications; Ensure submissions comply with applicable regulations and guidance documents; Advise team members on changing regulations and compliance requirements; Maintain the Clinical Trial Management System and ensure [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Trial Coordinator pro Jahr?
Als Clinical Trial Coordinator verdient man zwischen EUR 40.000,- bis EUR 70.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Trial Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 13 offene Stellenanzeigen für Clinical Trial Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Trial Coordinator Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Clinical Trial Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Trial Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Trial Coordinator Stellenangebote:
- Milteny GmbH (1 Job)
- IQVIA (1 Job)
- Rapid Trials (1 Job)
- Sanofi (1 Job)
- Medpace (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Coordinator Jobs werden derzeit in Bayern (4 Jobs), Nordrhein-Westfalen (2 Jobs) und Hessen (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Coordinator Jobs?
Clinical Trial Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
