Global Start-up Specialist

As a key member of our global team, you will have the opportunity to contribute to the success of our company and advance your career. You will be responsible for overseeing all aspects of start-up execution and management, with a focus on pro-active solutions-focused approaches to challenges.Required Skills and Qualifications:BA in Life Sciences,...

Startup Specialist RoleThis position involves collaborating with investigative sites to ensure a seamless start-up process and ongoing maintenance.Key Responsibilities:Maintain awareness of regulatory legislation and guidance in assigned countries.Coordinate data collection and submissions to authorities.Prepare and review study documentation and...

SSU responsibilities:- Coordinate guide and assist with all start up activities prior to site activation, including but not limited to:- Site Informed Consent Form (ICF) localization and guidance in line with regulatory/health authority requirements.- Ethics Committee information, meeting dates & costs.- Ethics & Governance submission processes.- Contracts &...

FSP - Regulatory & Start Up Specialist page is loaded## FSP - Regulatory & Start Up Specialistlocations: São Paulo, Braziltime type: Full timeposted on: Posted Todayjob requisition id: R Under moderate supervision, the **Site Activation Specialist** executes the feasibility, site identification regulatory, start-up, and maintenance activities in...

Study Start up Specialist I, IQVIA Biotech Join to apply for the Study Start up Specialist I, IQVIA Biotech role at IQVIA Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and...

Study Start up Specialist I Apply locations São Paulo, Brazil Time type Full time Posted on Posted Yesterday Job Requisition ID R1500196 Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project...

Job DescriptionWe are seeking a highly skilled Regulatory Specialist to join our team. As a key member of the team, you will play a critical role in ensuring compliance with regulations and facilitating the start-up process for clinical trials.Key ResponsibilitiesServe as a Single Point of Contact (SPOC) for assigned studies, working closely with project...

Job SummaryWe are seeking a highly skilled professional to oversee the start-up process of our clinical trials. This role plays a crucial part in ensuring seamless trial execution.Key Responsibilities:Manage and successfully execute global start-up activities.Perform quality checks on submission documents and site essential documents.Develop and approve...

OverviewOur LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo This position plays a key role in the study start up process at Medpace.ResponsibilitiesEfficiently manage and successfully execute all aspects of global...

Overview Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo This position plays a key role in the study start up process at Medpace. Responsibilities Efficiently manage and successfully execute all aspects of global...