Macarena F. Email & Phone Number

Ontario, Canada

Oversee and lead the Americas Site Intelligence Specialist team which is currently located across Canada, Mexico & Brazil

Kingston, Ontario, Canada

Collaborate with different functions and departments to establish category-wide feasibility and enrollment strategies within Inflammation and Immunology clinical research.

Kingston, Ontario, Canada

Partnering with Clinical Operations roles, Clinical Lead and CRO to help enable the predictable delivery of Pfizer’s portfolio.Responsible for driving rapid, accurate and robust assessments of program and protocol feasibility, including timing of key start-up and recruitment milestones and patient recruitment strategies.

Santiago, Región Metropolitana De Santiago, Chile

Partnering with Clinical Operations roles, Clinical Lead and CRO to help enable the predictable delivery of Pfizer’s portfolio.Responsible for driving rapid, accurate and robust assessments of program and protocol feasibility, including timing of key start-up and recruitment milestones and patient recruitment strategies.

Santiago, Región Metropolitana De Santiago, Chile

Responsible for in country site management and clinical/scientific oversight activities of assigned clinical trials to ensure patient safety and quality study execution according to applicable laws, GCP and Pfizer standards. Accountable for managing investigator site relationships to ensure effective delivery of clinical trials, safeguarding the quality of investigator sites and maintaining investigator and study coordinator engagement.

Santiago, Chile

Expand clinical research infrastructure in local markets from Chile and Peru, and contribute with the recommendation of investigational sites incorporating feedback from internal stakeholders. Mitigate deficiencies and support quality improvement in INSPIRE sites.Shape local clinical research environment, promoting GCP ethics and investigator training.Manage relationships with external stakeholders (investigators, regulatory authorities, ethics committees, etc) in collaboration with other Pfizer roles.Support implementation of Investigator Networks.

Management of studies and investigator sites, ensuring protection and well being of human subjects along with compliance with clinical protocol, ICH-GCP and local regulations.Involvement in the process of conducting a clinical trial, from regulatory phase to site close out activities. Verification that trial data is accurate and complete. Performing of varied monitoring activities, like regulatory submissions, site initiation and ongoing site visits, communicating with investigators and roles involved in the conduction of the clinical trial.

Pfizer Chile S. A.

Support quality in clinical trials area, implementing ways of process improvement, providing training and supervising compliance with global and local regulations.

Santiago Metropolitan Region, Chile