6 Jobs für Clinical Trials Coordinator
Stellenangebote Clinical Trials Coordinator Jobs
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 [. .. ] experience Working knowledge of Safety Databases (Argus is desirable) Demonstrate advanced knowledge of medical terminology, global safety reporting requirements and Good Clinical Practice (GCP) Guidelines Exposure to working on global trials as part of a multidisciplinary team Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-l V clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement [. .. ]
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 [. .. ] responsibilities as assigned, including site Qualification Visits, prepping/ consultation support for site audits, etc. Qualifications Minimum a Bachelor of Science in health-related field; Minimum 1 years site and clinical trials experience (more experience for the more senior positions required) ; CRA experience is an asset; Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred; Knowledge of medical terminology and clinical patient management preferred; Fluency in English; Demonstrated organizational and prioritization skills; Excellent oral and written [. .. ]
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 [. .. ] monitoring visits across Germany. Why Join Us? Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring. Gain handson exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills. Benefit from formal training programs, modern clinical systems, and continuous learning opportunities. Enjoy a flexible work model, competitive benefits, and a culture that values collaboration, quality, and wellbeing. At Fortrea, we welcome ambitious clinical research professionals who are ready to [. .. ]
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 of [...]
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[...] clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs) , International Council for Harmonization (ICH) Guideline for Good Clinical [. .. ] all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS Standard Operating Procedures (SOPs) and ICH GCP. Maintain the ethical and scientific integrity of clinical trials by verifying data within electronic systems and paper records (as applicable) to ensure the accessibility, completeness and accuracy of data submitted by study sites. Monitor site adherence to ICH GCP and local regulations, including compliance with the principles of ALCOA to maintain data integrity and reliability. Where required, provide training [. .. ] 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
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 [. .. ] Management Biostatistics Data Management Clinical Data Interpretation Medical Writing Soft Skills Leadership Communication Presentation Organizational Skills Industry Keywords Life Sciences Clinical Trial Lifecycle Investigational Review Boards External Clinical Vendors Pivotal Trials #J-18808-Ljbffr 01448414 [. .. ]
Job vor 2 Tagen bei Neuvoo.com gefunden
The Medical Affairs Company (TMAC)
[. .. ] 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 [. .. ] party vendor. Develop, communicate, and execute Site Engagement Strategy/ Plan working closely with the Companys Clinical Team and key 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 [. .. ] 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 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 6 offene Stellenanzeigen für Clinical Trials Coordinator Jobs.
In welchen Bundesländern werden die meisten Clinical Trials Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Trials Coordinator Jobs werden derzeit in Bayern (4 Jobs), Baden-Württemberg (1 Jobs) und Thüringen (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Trials Coordinator Jobs?
Clinical Trials Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
