Experteer OverviewAs a key member of IQVIA’s contracting team, you will shape global contracting strategies for sponsors and multi‑protocol studies. You will support start‑up contracting activities, including investigator grants, budget templates, and contract language, ensuring alignment with
Experteer OverviewIn this role you will develop and drive global contracting strategies for sponsor trials, coordinating with study teams and regional stakeholders to enable efficient study initiation. You will craft investigator grants, contracting language and budgets,
Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Sponsor Requirements Budget building within France
Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Sponsor Requirements: Budget building within France
Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Sponsor Requirements: Budget building within France
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
As a pharmaceutical support industry leader, UBC is dedicated to empowering health solutions for a better tomorrow. We are committed to improving patient outcomes and advancing healthcare. At UBC , we offer services that enhance the
Experteer Overview In this role you support the clinical research team to run studies in line with GCP, SOPs, and protocols, while respecting budgets and timelines. You own startup activities and document management, ensuring regulatory submissions
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership,
The Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned sites, ensuring site compliance with Good Clinical
The Clinical Research Associate is responsible for the feasibility, initiation, monitoring, and close-out of investigative sites. Major responsibilities include ensuring the safety and well-being of study participants at assigned sites, ensuring site compliance with Good Clinical
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership,
The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership,
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of
Responsibilities Manage research activities at sites participating in Worldwide’s clinical research projects, predominantly registries and other types of non‑interventional/observational studies. Oversee all stages of the clinical study, including identifying potential sites, performing study start‑up activities such
Job Summary Senior Chief Research Associate (Sr CRA) based in Italy, responsible for independent site monitoring, oversight, and management of clinical trials to ensure compliance with protocols, GCP, and sponsor requirements. Works closely with US and
Job Description Summary The CRA is an important member of the Alira Health Clinical team. The CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; providing oversight, leadership, and guidance
Job Summary Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Project Manager - Make an Impact at the Forefront of Innovation The Project Manager serves as the Project Lead and primary sponsor contact and is
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join us as a Senior Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Senior Clinical Trial Manager is accountable for achieving the final clinical