Parexel
Parexel has an exciting opportunity for a document specialist! The Document Specialist I will provide document technology support on Medical Writing projects as appropriate. Some specific responsibilities include compilation of appendices to clinical study reports and similar documents, document formatting…
The Trial Master Files Records 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 TMF management,…
PXL has an exciting FSP opportunity for a Senior Issue Lead. The Senior Issue Lead will ensure the investigations are conducted thoroughly, within required timelines and to compliance requirements including ensuring the adequacy of root cause analysis and appropriateness of…
The Local Study Associate Director (LSAD) leads Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Client Procedural Documents, international guidelines such as ICH GCP as…
Job Summary The Patient Compensation Lead in Clinical Development & Operations will be responsible for ensuring all processes and vendors are in place to enable participant compensation, reimbursement, and travel services. This role will be accountable for vendor performance, serve…
Job Summary The Patient Compensation Lead in Clinical Development & Operations will be responsible for ensuring all processes and vendors are in place to enable participant compensation, reimbursement, and travel services. This role will be accountable for vendor performance, serve…
Primary Location: Canada, Ontario, Remote Job ID R0000035728 Category Clinical Trials ABOUT THIS ROLE Job Summary The Patient Compensation Lead in Clinical Development & Operations will be responsible for ensuring all processes and vendors are in place to enable participant…
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,…