Study Start Up Associate

Job Opportunities in Clinical Research ManagementWe are seeking a highly skilled individual to join our team as a Clinical Study Start-up Associate II. As a key member of our team, you will be responsible for preparing and submitting regulatory documents for clinical trials.Key Responsibilities:Preparation and submission of regulatory documents according to...

Job Summary:As a Clinical Research Associate, you will collaborate with the global study team to ensure timely start-up activities at assigned sites. Your key responsibilities include site selection visits and verifying site eligibility for specific studies.Key Responsibilities:Support country strategy in collaboration with the SSU Team Lead, SSU Manager,...

Job OverviewWe are seeking a skilled professional to fill the role of Study Start-up Specialist. In this position, you will be responsible for overseeing Site Activation activities in accordance with local and international regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines.Your primary duties will...

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...

Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-basedRegulatory Submissions Managerto join our Study Start Up team in Sao Paulo 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 grow your...

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. If you want an exciting career where you use your previous expertise and can develop and...

ICON plc is a world-leading healthcare intelligence and clinical research organisation.From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.With our patients at the centre of all that we do, we help to accelerate the development of...

OverviewJoin to apply for the Clinical Start-Up & Trial Lead role at Fortrea.The Clinical Start-Up & Trial Lead (Start-Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site initiation...

Overview Join to apply for the Clinical Start-Up & Trial Lead role at Fortrea . The Clinical Start-Up & Trial Lead (Start-Up + CTL) is responsible for the strategic planning, coordination, and oversight of clinical trial start-up activities as well as the ongoing execution of clinical studies. This hybrid role ensures operational excellence from site...