Parexel
Partially Remote Must work 50% in office Burlington, Ontario Job Summary: Optimizes clinical research support activities by providing smart business solutions to complex contractual, compensation and payment structures thereby achieving success in all business aspects of Clinical Operations. Key Responsibilities…
Parexel FSP is seeking a Document Specialist for an exciting opportunity in Canada. This role requires strong experience with publishing software and preferably ISI toolbox experience. Key Accountabilities Compilation and publishing Compile appendices to clinical study reports in compliance with…
Job Summary: Optimizes clinical research support activities by providing smart business solutions to complex contractual, compensation and payment structures thereby achieving success in all business aspects of Clinical Operations. Key Responsibilities Clinical Trial Budget Management Develop budgets for clinical trials…
Key Accountabilities Database Administration and Maintenance Install, configure, upgrade, and patch supported database systems (Oracle 10g–19c, PostgreSQL, or MS SQL Server) Perform database and schema refresh operations using native tools (e.g., Oracle exp/imp, Expdp/Impdp; pgdump/pg*restore; SQL Server backup/restore) Implement database…
Parexel is seeking an experienced Global Regulatory Labeling Manager to collaborate with a dedicated client team and oversee complex global labeling initiatives. In this role, you will lead and coordinate labeling activities across foundational and non foundational markets, ensuring compliance…
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…