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
Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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 devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC, we provide services to enhance the entire
Job SummaryMedpace 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 the
Experteer OverviewIn this CRA role, you will independently conduct site monitoring for clinical trials and provide guidance to the monitoring team to ensure compliance and quality. You will collaborate with cross-functional teams to address site questions,
Job SummarySenior 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 EU
Job Description SummaryThe 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 in
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,
Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you. Join our global team dedicated to innovation and initiative, where
Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Project Manager - Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Senior Project Manager - Make an Impact at the Forefront of Innovation The Senior Project Manager serves as the Project Lead and primary sponsor contact
Work Schedule Standard (Mon-Fri) Environmental Conditions Office 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 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 Senior Clinical Team Manager PPD’s (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life
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