22 Jobs für Clinical Trial Coordinator
Stellenangebote Clinical Trial Coordinator Jobs
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 [...]
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[...] 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 25.10.2025 bei Jobleads gefunden
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Frankfurt, Hesse
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 accelerate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 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 [...]
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[...] 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 [...]
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[...] 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
Associate Clinical Trial Manager (PhD) - Neuroscience/ Ophthalmology
• 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 01.07.2025 bei Jobleads gefunden
• München, Bayern
Clinical Trial Site Relationship
Coordinator Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our [. .. ]
Neu Job vor 4 Std. 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 drive [...]
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[...] 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 [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Sanofi
• Berlin
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 drive [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ]
Neu Job vor 4 Std. bei Neuvoo gefunden
Parexel
Clinical Trial Specialist/ Senior Clinical Trial Associate
• Berlin
When our values align, theres no limit to what we can achieve. Parexel is beginning to search for an experienced Senior
Clinical Trial Administrator to join one of our key [...]
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[...] sponsors in the Clinical Trial Specialist. In this role you will provide technical and administrative support to the clinical study teams responsible for clinical trial execution. Some specifics about this advertised role Support moderately complex clinical study activities in support of the Clinical [. .. ] are a few requirements specific to this advertised role. At least 2 years of experience (3yrs preferred) in clinical studies (Pharmaceutical Industry Experience Preferred) . Previous site monitoring or study coordinator experience is preferred. Working knowledge of Good Clinical Practices (GCP) regulations and Standard Operating Procedures. Understanding of study phases and general knowledge of how they apply to clinical development. Demonstrated ability to work independently and in a team environment. Working knowledge of electronic Systems including Trial Master File, CTMS, etc. [. .. ]
Job gestern bei Neuvoo gefunden
Georgetown University in Qatar
• Ingelheim am Rhein, Rhineland- Palatinate
Work-Life-Balance
[. .. ] close-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 The Clinical Research Coordinator serves as clinical research coordinator for phase I, II, and III oncology clinical trials conducted in the Clinical Research Management Office (CRMO) of Lombardi Comprehensive Cancer Center. Incumbent duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines for minimal risk studies. Schedule and coordinate study-related procedures and assessments while maintaining protocol integrity and patient safety and in accordance with Good Clinical Practice (GCP) guidelines. Assist with triaging [. .. ]
Job vor 6 Tagen bei Neuvoo.com gefunden
Verbatim Pharma
Coordinator
• Berlin
Verbatim Pharma are working with a global company based in Berlin. The company is a global service partner for pharmaceutical and biotech firms, specialising in
clinical trial services. They [...]
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[...] have a great company culture that is a friendly, energetic and a multi-cultural. The company is home to employees from various backgrounds that speak a range of languages. If you have a forward-thinking attitude and are ready to go the extra mile then this could be [. .. ]
Job am 11.11.2025 bei Neuvoo.com gefunden
Medpace
• Munich
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 [. .. ] employing more than 5, 000 people across 40+ countries. Job Summary Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator/ Study Start-up Specialist to join our Clinical Operations team in Munich. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Entry-level positions with permanent contract are available for recent graduates. Responsibilities Prepare, review, and file clinical trial [. .. ]
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 [. .. ]
Job am 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Essen
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 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Stuttgart
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 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Berlin
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 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Cologne
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 14.10.2025 bei Neuvoo.com gefunden
Medpace
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 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 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Munich
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 14.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Düsseldorf
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 04.10.2025 bei Neuvoo.com gefunden
Medpace
Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience
• Hamburg
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 [. .. ]
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 22 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:
- Medpace (10 Jobs)
- Sanofi (2 Jobs)
- Parexel (1 Job)
- Georgetown University in Qatar (1 Job)
- Verbatim Pharma (1 Job)
In welchen Bundesländern werden die meisten Clinical Trial Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Coordinator Jobs werden derzeit in Berlin (4 Jobs), Nordrhein-Westfalen (3 Jobs) und Bayern (3 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Coordinator Jobs?
Clinical Trial Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
