Global Start-Up Manager

Job OverviewThe Global Start-up Manager oversees the efficient and successful execution of all global start-up aspects, ensuring quality control over submission documents and site essential documents.Key QualificationsAt least 4 years of experience in regulatory submissions/start-up management (leading project teams);Knowledge and experience of Clinical...

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...

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,...

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 &...

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...

**Become a Local Expert in Clinical Trial Start-Up**Be the go-to person for investigative sites, guiding them through the critical start-up phase of clinical trials in a global perspective (focused on North America projects).Your expertise in local regulations will ensure timely and compliant submissions, directly impacting the speed and success of vital...

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...