Job Purpose/ Summary: Independently manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. Interact with, assist,
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Alnylam Pharmaceuticals is seeking a Senior Manager, Study Start-up to join our dynamic and growing team. The Senior Manager, Study Start-up partners closely with the Clinical Operations study team leading global study start-up and site activation activities in Phase I-III and real-world evidence
Description The Department of African Diaspora Studies (ADS) invites applications for a tenure-track appointment beginning Fall 2027. Rank open, but Assistant Professor/Associate Professor preferred. Research and teaching interests might include, but are not limited to: environmental studies and
Working Calendar: 187 Days/7 Hours Job Description: Attached Salary Schedule: III (Attached) Estimated New Hire Salary Range: $48,479.56 - $98,587.95 *As per board approved salary placement rules* 26-27 Teacher Transfer Instructions: Current JCPS teachers who wish
Regulatory Submissions Coordinator Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. This position works both independently and collaboratively with a team to
Regulatory Submissions Intern Our clinical operations activities are growing rapidly, and we are seeking a full-time, office-based intern to support our Regulatory Submissions team within our Site Activation and Maintenance (SAM) Department for fall 2026. This
Regulatory Submissions Coordinator Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This position works both independently and collaboratively with a team to meet
Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus proprietary platform connects an entire ecosystem
Tempus AI is seeking a Study Start-Up Manager in Chicago to oversee study start-up and site activations for key research sites. The candidate will coordinate with various teams to enhance patient access to clinical trials through the TIME program. Qualified
Clinical Research Coordinator Our clinical operations activities are growing rapidly, and we are currently seeking talent Clinical Research Coordinators to join our Study Start-up team. This position works both independently and collaboratively with a team to meet common
Study Start-Up Project Manager Do you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing
Director Of Study Start-Up We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the Clinical Operations leadership team and requires a strong understanding of
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 contractual/budgetary guidelines. May also include maintenance activities.
Tempus Clinical Research Coordinator Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus proprietary platform
Study Start Up Associate - Home-based in Australia ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility,
Regulatory Submissions Coordinator Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. This position works both independently and collaboratively with a team to
Study Start-Up Manager We are looking for a Study Start-Up Manager with extensive experience to lead clinical study start-up activities. This role requires a strong background in regulatory processes, site management, and expertise in ensuring compliance with local and international guidelines, particularly
Study Start-Up Project Manager Do you enjoy working in a fast-paced environment where you are empowered to make strategic decisions and contribute to a growing and profitable company? Join us at Medpace! Our clinical operations activities are growing
Regulatory Submissions Coordinator Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Study Start-up team. This position works both independently and collaboratively with a team to