When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Job Overview: Our FSO team is seeking an Oncology Clinical Project Manager II or Sr Project Manager to join our growing team. This role requires 3+ years of global project management experience, with mandatory experience in
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Clinical Trial Psych Rater - Portuguese Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs,
Planet Pharma is supporting a leading clinical research organisation in hiring experienced Asegúrese de enviar su solicitud rápidamente para maximizar sus posibilidades de ser considerado para una entrevista. Lea la descripción completa del puesto a continuación. Mobile
Job Overview : Summary of Responsibilities : - To serve as contact for project team and investigative sites, conduct site contacts and document contacts for assigned sites as required per study guidelines, including creating contact reports
Summary of Responsibilities : - Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. - Conducts site monitoring
Principal Clinical Research Associate Please submit your CV in English for Quickest Review Process! Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so,
Job Overview Site Navigators II plays a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point
Clinical Specialist Interventional Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. - Spain POSITION SUMMARY : The Spanish Clinical & Medical Affairs (CMA)
Clinical Specialist Interventional - Spain Siga leyendo para descubrir lo que necesitará para tener éxito en este puesto, incluyendo habilidades, cualificaciones y experiencia. POSITION SUMMARY : The Spanish Clinical & Medical Affairs (CMA) Specialist Interventional reports
Organizational Overview Smile Train is the world’s leading cleft focused organization. Our goal is to transform the lives of every person impacted by a cleft lip or palate. We train and support doctors and medical professionals
Looking for a way to make an impact and help people? - Join PacificSource and help our members access quality, affordable care!_ PacificSource is an equal opportunity employer. All qualified applicants will receive consideration for employment
The Clinical Trial Manager II (CTM II), Dermatology & Rheumatology, is responsible for the operational management and oversight of the clinical investigative sites as well as the clinical monitoring deliverables of clinical trials. This includes but
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Essential Functions Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to
Job Function : R&D Operations Job Sub Function : Clinical Trial Project Management Job Category : Professional All Job Posting Locations : BR031 São Paulo, MX904 Boulevard Adolfo Ruiz Cortines The Lead, Trial Delivery Manager (TDM)
More specifically, the Start-Up, Project Manager - Manage the end-to-end study start-up process, including site selection, regulatory submissions, site contracting and budgeting, and site activation. - Define start-up strategy and timelines in collaboration with the Project