Key Accountabilities:Contracting deliverables Exercise good judgment in balancing the risks to the client in making budget and contractual decisions against the impacts to client clinical trial timelines Follow client processes to develop, negotiate, track and execute global clinical study agreements…
The Study Operations Manager I (SOM I) has responsibilities for study and regional or specific country level activities from study startup through conduct and study close on one or more studies, providing leadership, strategic planning, and organization skills to ensure…
The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical…
The Start Up Project Manager is responsible for defining, developing and delivering the global start up project strategy by partnering with roles across GSSO, CD&O, Global Regulatory Submissions and others as required. The SUPM will be assigned to one or…
The Study Operations Manager I (SOM I) has responsibilities for study and regional or specific country level activities from study startup through conduct and study close on one or more studies, providing leadership, strategic planning, and organization skills to ensure…
The Investigative Site Budget Specialist (ISBS) is responsible for supporting the overall budget development process for site facing budget templates, which includes working independently with business partners to develop global clinical site budgets, coordination of the multiple activities required to…
The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical…
The Investigative Site Budget Specialist (ISBS) is responsible for supporting the overall budget development process for site facing budget templates, which includes working independently with business partners to develop global clinical site budgets, coordination of the multiple activities required to…
Parexel is looking for a sponsor dedicated Sr Study Contract Manager! This is a hybrid role with 3 days per week based in Mississauga Ontario Canada. The Senior Study Contract Manager (Sr.SCM) play an important role in driving the costings…
Canada, Remote Job ID R0000033654 Category Clinical Trials ABOUT THIS ROLE Parexel is looking for a sponsor dedicated Sr Study Contract Manager! This is a hybrid role with 3 days per week based in Mississauga Ontario Canada. The Senior Study…
Job Summary: The Trial Master Files Record Specialist (TRS) is responsible to provide operational expertise to the core trial team, oversees the implementation of the TMF strategy for the trial and supports the core trial team in all aspects of…