Clinical Research Start-Up Professional

Position SummaryThe 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 through to study close-out, serving as the primary...

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,...

Are you a detail-oriented and organized professional looking for a new challenge in clinical research?Clinical Research Associate (CRA) RoleAbout the JobThe role of Clinical Research Associate is a critical component of our team, responsible for ensuring that clinical research studies are conducted in accordance with widely accepted clinical practices.We are...

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:Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Study Start-Up Manager (Regulatory Submissions Manager) to support our growing Study Start-Up/Regulatory Submissions team at Medpace This position plays a key role in the clinical trial management process at Medpace. If you want an...

**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...

Clinical Research Associate (CRA)The primary responsibility of a Clinical Research Associate (CRA) is to oversee clinical trials and ensure they are conducted in accordance with Good Clinical Practice (GCP) guidelines.About the RoleWe are seeking an experienced and detail-oriented CRA to join our team. The successful candidate will be responsible...

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...

Job TitleClinical Research Associate II / Senior Clinical Research Associate (CRA)">We are seeking a highly skilled and experienced Clinical Research Associate to join our team in conducting clinical trials.The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and clinical trial...

Job Title:Senior Clinical Research AssociateJob Description:We are seeking a skilled and experienced Senior Clinical Research Associate to join our team. As a key member of our clinical research operations, you will be responsible for conducting site visits, managing study documents, and collaborating with project teams to ensure the successful execution of...