, office-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role... in the study start up process at Medpace. If you want an exciting career where you use your previous expertise and can...
-based Regulatory Submissions Manager to join our Study Start Up team in Buenos Aires! This position plays a key role in the... study start up process at Medpace. If you want an exciting career where you use your previous expertise and can develop...
and administrative documentation to support business development and enable study initiation and maintenance, as required. IQVIA...
documentation to support business development and enable study initiation and maintenance, as required.IQVIA is a leading global...
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 accelerate the int...
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 accelerate the glo...
future of clinical development We are currently seeking a Manager, Study Start-Up to join our diverse and dynamic team.... As a Manager of Study Start-Up at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring...
future of clinical development. We are currently seeking a Manager, Study Start-Up to join our diverse and dynamic team.... As a Manager of Study Start-Up at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring...
future of clinical development We are currently seeking a Manager, Study Start-Up to join our diverse and dynamic team.... As a Manager of Study Start-Up at ICON, you will lead and oversee the start-up activities for clinical trials, ensuring...
aspects of the Site Start-Up deliverables of the assigned projects. Accountable for the delivery of activation-ready study... fundamental issues pertaining to Site Start-Up, project regulatory pathway, successful patient enrollment, interpret data...
the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up... role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study. The CTM oversees...
), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure... in investigator meetings as needed. 4 Responsible for executing activities within site initiation and start-up, preparation...
leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected... to protocol, SOPs, ICH GCP and country regulations This may include data management, study start up, patient recruitment, medical...
fundamental issues pertaining to Site Start-Up, project regulatory pathway, successful patient enrollment, interpret data... quality standards, and policies and procedures are followed. Provides oversight of all project start-up deliverables...
Operations department. This position will report to the LatAm Senior Contract Manager and will play a key role in the study start...-up and clinical trial management processes at Medpace. The Contract Manager will play a key role in advancing the start...
Operations department. This position will report to the LatAm Senior Contract Manager and will play a key role in the study start...-up and clinical trial management processes at Medpace. The Contract Manager will play a key role in advancing the start...
for end-to-end project management from start-up through to closeout activities. Tasks & Responsibilities: Services...Clinical Trial Manager – Sponsor Dedicated. Clinical Project Management services provide management of a clinical...
: Lead global/regional clinical trials from start-up through close-out. Develop and execute study management plans aligned.... IQVIA Biotech is seeking an experienced Clinical Project Manager based in Argentina to lead and deliver innovative clinical...
aspects of the Site Start-Up deliverables of the assigned projects. Accountable for the delivery of activation-ready study..., Clinical, Data Management and Medical Writing. Identifies and evaluates fundamental issues pertaining to Site Start-Up...
. Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery... start up, patient recruitment, medical monitoring, pharmacovigilance and Quality Assurance (QA). Supports Inspection...