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
Who We Are Celebrating 40+ Years! Theradex Oncology is a full-service CRO, conducting early and late-phase oncology trials in the U.S, Europe and Asia. Theradex Oncology was founded in 1982, when we were awarded the Clinical
Shared Services: Clinical Trial Center- (Full-Time, Day Shift) - Job Summary: The Study Start Up Specialist is responsible for reviewing clinical research studies to determine whether the study is a qualifying study pursuant to Medicares National Coverage Determination (310.10). Coordinates the
SS: Clinical Trial Center- (Full-Time, Day Shift) - Job Summary: The Study Start Up Specialist Senior is responsible for reviewing clinical research studies to determine whether the study is a qualifying study pursuant to Medicares National Coverage Determination (310.10). Mentors and
Study Start Up Manager 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, and inclusion are at
Description The Department of German Studies invites applications for a 1-year term appointment with the possibility of renewal in any area of German Studies, beginning Fall 2026. Near-native fluency in German is required. Assistant Professor (Ph.D.) preferred; Instructor
Description The Department African Diaspora Studies invites applications for a two-year Andrew W. Mellon Postdoctoral Fellowship beginning Fall 2026. Eligible candidates must have received their terminal degree no earlier in 2023 or later. We seek interdisciplinary/transdisciplinary scholars
Study Start-Up Clinical Research Associate, Sponsor Dedicated Durham, United States of America | Full time | Field-based | R1513886 IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and
Study Start Up Operations Manager - Full Time - Wolf River Germantown, TN Manager, Study Start Up Operations At West Cancer Center, we are committed to advancing innovative cancer research while delivering compassionate, patient-centered care. Our research teams play a
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 Title Support Project Management, Regulatory, and Contract and Legal in all site-related start-up activities. Establish relationships with study personnel at sites and act as main Alimentiv contact during site start-up. Prepare, distribute and follow-up on start-up documents with sites.
Associate Director, Clinical Operations Program Lead, Study Start-up and Feasibility The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust
Study Start Up Associate 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, and inclusion are at
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
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
Global 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
Oncology Study Start-Up Manager The Study Start-Up Manager (SSU Manager) is responsible at the country level for managing and conducting start-up activities in compliance with AstraZeneca procedures, documents, local and international guidelines such as ICH-GCP, and relevant regulations. The SSU Manager
Global 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
Senior Manager, Global Site Start-Up Lead (SSU Lead) The Senior Manager, Global Site Start-Up Lead (SSU Lead) is responsible for driving the global execution of site activation for complex, high profile clinical trials, performing the role with high-degree
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