Global Clinical Start Up Manager

About the RoleWe are seeking a highly skilled Clinical Start-up Manager to join our team at Resourcing Life Science. As a Clinical Start-up Manager, you will be responsible for leading cross-functional project teams globally for assigned studies in the start-up phase.Key ResponsibilitiesEnsure adherence to Good Clinical Practices, investigator integrity, and...

About the RoleWe are seeking a highly skilled Clinical Start-up Manager to join our team at Resourcing Life Science. As a Clinical Start-up Manager, you will be responsible for leading cross-functional project teams globally for assigned studies in the start-up phase.Key ResponsibilitiesEnsure adherence to Good Clinical Practices, investigator integrity, and...

**Job Overview**As a Clinical Start Up Manager with Resourcing Life Science, you will lead cross-functional project teams globally for assigned studies in the start up phase. Your primary focus will be on ensuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.**Key Responsibilities**Monitor study...

**Job Overview**As a Clinical Start Up Manager with Resourcing Life Science, you will lead cross-functional project teams globally for assigned studies in the start up phase. Your primary focus will be on ensuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.**Key Responsibilities**Monitor study...

**About Our Client**Our client is a leading Global Contract Research Organization (CRO) providing comprehensive solutions for pharmaceutical and biotech companies worldwide. They offer a full-service approach encompassing clinical and non-clinical development, peri-approval, and market access.**Job Overview**As a Clinical Start Up Manager, you will lead...

**About Our Client**Our client is a leading Global Contract Research Organization (CRO) providing comprehensive solutions for pharmaceutical and biotech companies worldwide. They offer a full-service approach encompassing clinical and non-clinical development, peri-approval, and market access.**Job Overview**As a Clinical Start Up Manager, you will lead...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at ICON. As a Study Start Up Associate, you will play a critical role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at ICON. As a Study Start Up Associate, you will play a critical role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key...

Job SummaryAt Sin Nombre, we are seeking a highly skilled Study Start-Up Manager to join our team. As a key member of our EU Center, you will be responsible for managing and coordinating Part 2 packages, ensuring timely submission to regulatory authorities. Your expertise will be crucial in driving the success of our clinical trials.Key...

Job SummaryAt Sin Nombre, we are seeking a highly skilled Study Start-Up Manager to join our team. As a key member of our EU Center, you will be responsible for managing and coordinating Part 2 packages, ensuring timely submission to regulatory authorities. Your expertise will be crucial in driving the success of our clinical trials.Key...

About the Role**Study Start Up Associate II**We are seeking a highly skilled and experienced Study Start Up Associate II to join our team at ICON. As a key member of our clinical trials team, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of...

About the Role**Study Start Up Associate II**We are seeking a highly skilled and experienced Study Start Up Associate II to join our team at ICON. As a key member of our clinical trials team, you will play a pivotal role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at ICON. As a key member of our clinical trials team, you will play a critical role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at ICON. As a key member of our clinical trials team, you will play a critical role in leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and...

**Job Summary**The Precision Medicine Group, LLC. is seeking an experienced Start Up Lead/Senior Start Up Lead to join our team. This role is responsible for the execution of site start-up activities and strategy planning, including the management and coordination of critical path planning, IRB/EC and CA/MoH submissions, and delivery of quality IMP release...

**Job Summary**The Precision Medicine Group, LLC. is seeking an experienced Start Up Lead/Senior Start Up Lead to join our team. This role is responsible for the execution of site start-up activities and strategy planning, including the management and coordination of critical path planning, IRB/EC and CA/MoH submissions, and delivery of quality IMP release...

**Job Overview**The Senior Study Start-Up Lead will be responsible for managing the global and/or regional submission of clinical trial applications for studies executed by Caidya on behalf of clients. This role requires the ability to independently compile, review, and approve essential study documents, as well as have a solid understanding of regulatory...

**Job Overview**The Senior Study Start-Up Lead will be responsible for managing the global and/or regional submission of clinical trial applications for studies executed by Caidya on behalf of clients. This role requires the ability to independently compile, review, and approve essential study documents, as well as have a solid understanding of regulatory...

Job Overview:The Senior Study Start-Up Lead will be responsible for managing the global and/or regional submission of clinical trial applications for studies executed by Caidya on behalf of clients. This role requires the ability to independently compile, review, and approve essential study documents and have a solid understanding of regulatory submission...

Job Overview:The Senior Study Start-Up Lead will be responsible for managing the global and/or regional submission of clinical trial applications for studies executed by Caidya on behalf of clients. This role requires the ability to independently compile, review, and approve essential study documents and have a solid understanding of regulatory submission...