15 Jobs für Clinical Trial Coordinator
Stellenangebote Clinical Trial Coordinator Jobs
Job gestern bei Stellen-Online.de gefunden
UCB Group
• Mettmann, 40822
Make your mark for patients We are looking for a Senior Principal Programmer (Statistical Computing Environment Business
Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and [...]
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[...] Reporting team, based in any of our Brussels (Belgium) , Monheim (Germany) , Raleigh (USA) , or Slough (UK) offices. About the role You will help clinical programming teams move to and work confidently within UCBs modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs. Who youll work with You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical ways [. .. ]
Job vor 4 Tagen bei Stellen-Online.de gefunden
Medpace
• München, 80331 Muenchen
Job Summary At Medpace, our European Pharmacovigilance (PV) activities are growing rapidly. As such, we are searching for motivated individuals to join our
Clinical Safety team in London. Working as [...]
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[...] part of a high performing group alongside Medical Monitors, Quality Assurance, Clinical Trial Management and others, this position plays a key role at Medpace to accomplish tasks and work on projects that are instrumental to the development of life changing medicines. If you want an exciting career where you can apply yourself to a variety of opportunities and develop new skills, then this [. .. ]
Job vor 4 Tagen bei Stellen-Online.de gefunden
Medpace
• München, 80331 Muenchen
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 vor 4 Tagen bei Stellen-Online.de gefunden
Medpace
• München, 80331 Muenchen
Job Summary 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 team in Germany, Munich. [...]
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[...] This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities across the DACH region. This position will [. .. ]
Job vor 4 Tagen bei Stellen-Online.de gefunden
Medpace
• München, 80331 Muenchen
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 2 Tagen bei Jobleads gefunden
• Lausanne, Waadt
Work-Life-Balance
[. .. ] and resource recovery, based in Prverenges, Switzerland. Founded in 2015 by engineers from cole Polytechnique Fdrale de Lausanne (EPFL) , ou. . . Mehr anzeigen Vers-chez-les-Blanc, Switzerland. [...]
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[...] Clinical Research Unit, Nestl Research. The Senior Clinical Trial Assistant (Sr. CTA) provides high-qualityoperational and administrative support to clinical trial. . . Mehr anzeigen Shape the future through scientific breakthroughs and innovation. As a Specialist Neuroscience at Nestl Research, your mission is to lead and contribute to research on the impact of nutrition in in. . . Mehr anzeigen For the development of our core strategic solutions, we are currently looking for a very experienced, top motivated, hands-on:. TECHNICAL COORDINATOR (SOFTWARE/ AUTOMATION) . The Technical Coordinato. . . Mehr anzeigen The International Institute for Management Development (IMD) has been pioneering leadership development for nearly 80 years. Founded by business for business, we are an independent university instit. . . Mehr anzeigen Vers-chez-les-Blanc, Switzerland. Clinical Research Unit, Nestl [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• München, Bayern
Are you ready to take the next step in your
clinical research career and transition into a Clinical Research Associate role? We are looking for motivated professionals with experience as [...]
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[...] a Study Nurse, Study Coordinator, Clinical Trial Assistant (CTA) , or In-House CRA who are eager to move into onsite monitoring and build a successful CRA career. You will contribute to the execution of clinical studies across a variety of therapeutic areas, including Oncology, Dermatology, Respiratory, Cardiology, and Diabetes, gaining broad exposure and handson experience while [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Berlin
Beratungs-/ Consultingtätigkeiten
The
Clinical Research Nurse is responsible for providing clinical nursing care for all study participants an accordance with departmental policies and procedures and established standards of nursing care and [...]
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[...] practice in Clinical Trial setting. Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• München, Bayern
The
Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance [...]
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[...] of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs) , International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP) , and applicable regulatory requirements. Key Responsibilities Conduct site qualification, initiation, routine monitoring and closeout visits across all trial phases in accordance with the Site Monitoring Plan, ensuring [. .. ] years of relevant clinical research experience, able to work independently, demonstrates proficiency in all aspects of the role. Relevant prior Pharma/ Biotech Sponsor employment or experience as a clinical study coordinator preferred. Experience in the drug discovery/ development process. Competencies Knowledge and understanding of clinical research processes, regulations and methodology. Understands clinical landscape with practical knowledge of a variety of medical settings and medical records management. Working knowledge of ICH/ GCP Guidelines and applicable local laws and regulations to ensure compliance [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Krailling, Bayern
Overview The
Clinical Development Operations
Coordinator (f/d/m) provides dedicated administrative and operational support to the Clinical Development and Clinical Operations functions. This role is ideal for an experienced [...]
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[...] coordinator who understands the pace, confidentiality, documentation standards and regulated environment of clinical drug development. Acting as the operational backbone of the CMO organization, the coordinator [. .. ] Key Responsibilities Provide highquality administrative support to Clinical Development, Clinical Operations and Regulatory Affairs leaders, including calendar management, meeting coordination, agenda preparation and followup tracking. Coordinate complex crossfunctional meetings, including trial team meetings, governance meetings, vendor meetings, Steering Committees, Advisory Boards and leadership reviews. Prepare, organise and distribute meeting agendas, presentations, prereads, minutes, action logs and followup summaries. Maintain awareness of key clinical milestones and proactively coordinate meeting cadence and preparation to support timely decisionmaking. Partner closely with Project Management to [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Senior Clinical Project Manager
Work-Life-Balance
Responsible for independently leading the
clinical trial study team. Managing global clinical trial activities on pivotal trial. Effectively communicates and guides clinical team members. Partners effectively with R D, Regulatory, [...]
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[...] Quality, Marketing/ Product stake-holders. Management of all clinical studies including developing project management plans. Identification, qualification, and training of investigators and teams. Responsible for the activities related to IRBs/ ECs, and clinical study vendors. Proactively manage the data management and data lock processes. Great site relationships with the PI and coordinator Requirements Bachelors degree in a Life Sciences discipline required Exceptional proficiency in professional English, with advanced medical and scientific writing skills Demonstrated experience authoring clinical study protocols Strong presentation and communication skills Comprehensive knowledge of the medical device clinical trial lifecycle In-depth understanding of medical device clinical research Solid [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Clinical Research Nurse
• Berlin
The
Clinical Research Nurse is responsible for providing clinical nursing care for all study participants in accordance with departmental policies and procedures and established standards of nursing care and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] practice in Clinical Trial setting. Key Accountabilities Coordinate and provide support and continuity for the allocated studies Supporting all study activities, documentation processes and special needs of a clinical study in conjunction with the Senior Clinical Research Coordinator, Clinical Research Coordinator Responsibility for subjects safety and medical data documentation according to the case report forms, study protocol and ICH/ GCP guidelines Organisation and Preparation of clinical studies, as listed below: Verification and maintenance of the file containing the volunteers informed consent forms Organisation of study specific materials and [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Senior Principal Programmer
• Monheim, Bayern
We are looking for a Senior Principal Programmer (Statistical Computing Environment Business
Coordinator) who is collaborative, detail-oriented, and compliance-minded to join our Programming, Visualization and Reporting team, based in [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] any of our Brussels (Belgium) , Monheim (Germany) , Raleigh (USA) , or Slough (UK) offices. About The Role You will help clinical programming teams move to and work confidently within UCBs modern Statistical Computing Environment. You will translate clinical reporting needs into well-governed study setups, support compliant platform operations, and help improve the way teams generate, validate, and deliver clinical trial analysis and reporting outputs. Who Youll Work With You will work with the Programming, Visualization and Reporting team, statistical programming teams, platform administrators, Biometrics partners, and business stakeholders. You will connect technical and business needs, support users through onboarding and daily operations, and help teams follow consistent, compliant, and practical [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
Clinical Research Associate m/w/d
• Heidelberg, Baden- Württemberg
Responsibilities Primary point of contact at the site level for both internal and external stakeholders Responsible for overseeing the quality, integrity and compliance of
clinical trial sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the protocol, SOPs, ICH GCP, and applicable regulatory requirements Conduct site qualification, initiation, routine monitoring and closeout visits across all trial phases Monitor site adherence to ICH GCP and local regulations Cultivate and sustain effective relationships with internal crossfunctional teams and external partners Prepare and submit [. .. ] years of relevant clinical research experience, able to work independently Demonstrated proficiency in all aspects of the role Relevant prior Pharma/ Biotech Sponsor employment or experience as a clinical study coordinator preferred Working knowledge of ICH/ GCP Guidelines and applicable local laws and regulations Proficient in navigating and utilizing multiple clinical systems (e. g. , CTMS, e TMF, RBQM dashboards) #J-18808-Ljbffr 01503677 [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
Site Engagement Manager, Immunology (Germany)
[. .. ] for providing operational expertise to sites through ownership/ management of Site Engagement Strategy. The scope of this role includes the following: Duties and Responsibilities: Define and implement [...]
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[...] strategies for engaging clinical sites and investigators. Characterize and understand the attributes of a good clinical site versus a poor performing site. Engage clinical sites to develop build and maintain relationships with investigators/ staff to ensure continued performance and capitalize on site expertise. Evaluate, screen and develop high quality investigative sites to support the [. .. ] internal stake holders throughout the life cycle of the Companys clinical trials. Support the Companys clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the Companys trials. Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication channels to create awareness of the Company and its activities thereby increasing their desire to partner with the Company. [. .. ] and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e. g. , clinical project manager, study director/ coordinator, clinical research associate, patient/ site engagement companies) . Qualified individuals will have a strong familiarity of and experience with clinical research and study site logistics. Scientific and/or clinical experience in Immunology, Autoimmune Disease, strongly preferred. Prior Pharmaceutical or Device industry experience as a Clinical Trial Liaison highly regarded. Candidates [. .. ]
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 15 offene Stellenanzeigen für Clinical Trial Coordinator Jobs.
In welchen Bundesländern werden die meisten Clinical Trial Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trial Coordinator Jobs werden derzeit in Bayern (8 Jobs), Baden-Württemberg (2 Jobs) und Berlin (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trial Coordinator Jobs?
Clinical Trial Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
