Parexel
The Site Care Partner is a crucial liaison for investigative sites throughout a study's lifecycle, responsible for site start up, activation, relationship management, recruitment, and quality assurance. This role also contributes to site selection, provides local intelligence, ensures site support,…
The Site Care Partner is a crucial liaison for investigative sites throughout a study's lifecycle, responsible for site start up, activation, relationship management, recruitment, and quality assurance. This role also contributes to site selection, provides local intelligence, ensures site support,…
Principal Biostatistician – Vaccines Therapeutic Area ========================================================= We are seeking a highly skilled FSP Statistician to support projects in the Vaccines Therapeutic Area within Research and Development. The successful candidate will collaborate closely with project and study teams, providing statistical…
Principal Biostatistician – Vaccines Therapeutic Area We are seeking a highly skilled FSP Statistician to support projects in the Vaccines Therapeutic Area within Research and Development. The successful candidate will collaborate closely with project and study teams, providing statistical expertise…
Primary Location: Canada, Ontario, Remote Job ID R0000034869 Category Clinical Trials ABOUT THIS ROLE Job Purpose: The Start Up Project Manager is responsible for defining, developing and delivering the global start up project strategy by partnering with roles across GSSO,…
Job Purpose: The Senior Clinical Research Associate I (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…
Job Purpose: Investigator Contracts Lead I (ICL I) is responsible for direct site facing contract and budget negotiations through contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies.…
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…