- Functioning as a Clinical Trial Manager (CTM) and National Clinical Trial Manager (NCTM) as per trial assignment. - Supporting delivery of trial activity at sites through leadership and/or training of CRAs.- Facilitating best practices through Q&A, problem solving and knowledge sharing.- Collaborating with relevant stakeholders.- Supporting compliance and quality at sites, within the country and across the trial according to ICH-GCP Guidelines, Standard Operating Procedures and other regulations and laws as applicable.- Supporting improvement including mentoring, training, GSM and/or cross-functional initiative participation, and taking a SME role in processes and/or systems.

- Managed and monitored clinical trial activity at investigator sites according to ICH-GCP Guidelines, the Standard Operating Procedures, and the approved protocol.- Functioned as a National Lead Clinical Research Associate (NLCRA) and Global Lead Clinical Research Associate (GLCRA) as per trial assignment

- Managed and monitored clinical trial activity at investigator sites according to ICH-GCP Guidelines, the Standard Operating Procedures, and the approved protocol.- Functioned as a National Lead Clinical Research Associate (NLCRA) and Global Lead Clinical Research Associate (GLCRA) as per trial assignment

- Managed and monitored clinical trial activity at investigator sites according to ICH-GCP Guidelines, the Standard Operating Procedures, and the approved protocol.- Functioned as a National Lead CRA/Assisting National Lead CRA as required.

- Ensured clinical trials in Canada and the USA were conducted in accordance with the Clinical Study Protocol, Standard Operating Procedures, Good Clinical Practice and applicable Regulatory requirements.- Functioned as a CRA, National Lead CRA, Assisting National Lead CRA as required.

- Managed all trial documents & all investigational product according to ICH-GCP Guidelines and Standard Operating Procedures for numerous trials in multiple therapeutic areas- Performed Clinical Project Manager duties

- Managed and monitored clinical trial activity at investigator sites according to ICH-GCP Guidelines, the sponsor's Standard Operating Procedures, and the approved protocol in Canada and in the USA for numerous sites in multiple therapeutic areas.- Pre-Study Visits - site selection- Initiation Visit Presentations - site preparation- Monitoring Visits - ongoing site management, source document verification and CRF review, Ensured timelines for database lock were met, investigational product accountability, regulatory file review- Co-monitoring Visits- Close-Out Visits- Audit Preparation

- Managed all trial documents & all investigational product according to ICH-GCP Guidelines and Standard Operating Procedures for numerous trials.

- Provided administrative support for clinical trial logistics and regulatory documentation according to ICH-GCP Guidelines and Standard Operating Procedures for numerous trials.- Designed payment ledgers & processing study related invoices.