Sara Fitzpatrick Email & Phone Number

Gualala, California, United States

Morrisville, Nc, Us

 Performs and coordinates all aspects of the clinical monitoring process to assess the safety and efficacy of investigational pharmaceutical and biological products with minimal supervision Completes pre-study, initiation, interim and close-out monitoring visits Initiates and maintained professional, collaborative relationships with physicians in various specialties, their research staff and the client pharmaceutical companies Presents medical/therapeutic background information, protocol adherence, adverse event reporting, good clinical practices and proper handling of various pharmaceutical investigational products Facilitates effective communication between physicians and the sponsor pharmaceutical companies through written, oral and/or electronic contacts Verifies proper administration of informed consent process at clinical sitesReviews and queries data on Case Report Forms and source documentsAdheres to monitoring plan and maintains site regulatory binder, and other site-specific and monitoring toolsVerifies appropriate reporting and documentation of adverse events, protocol deviations and subject enrollment

Fair Lawn, New Jersey, Us

 Performs and coordinates all aspects of the clinical monitoring process to assess the safety and efficacy of investigational pharmaceutical and biological products with minimal supervision Completes pre-study, initiation, interim and close-out monitoring visits Initiates and maintained professional, collaborative relationships with physicians in various specialties, their research staff and the client pharmaceutical companies Presents medical/therapeutic background information, protocol adherence, adverse event reporting, good clinical practices and proper handling of various pharmaceutical investigational products Facilitates effective communication between physicians and the sponsor pharmaceutical companies through written, oral and/or electronic contacts Verifies proper administration of informed consent process at clinical sitesReviews and queries data on Case Report Forms and source documentsAdheres to monitoring plan and maintains site regulatory binder, and other site-specific and monitoring toolsVerifies appropriate reporting and documentation of adverse events, protocol deviations and subject enrollment

Wilmington, Nc, Us

 Performed and coordinated all aspects of the clinical monitoring process to assess the safety and efficacy of investigational pharmaceutical and biological products with minimal supervision Completed pre-study, initiation, interim and close-out monitoring visits Initiated and maintained professional, collaborative relationships with physicians in various specialties, their research staff and the client pharmaceutical companies Presented medical/therapeutic background information, protocol adherence, adverse event reporting, good clinical practices and proper handling of various pharmaceutical investigational products Facilitated effective communication between physicians and the sponsor pharmaceutical companies through written, oral and/or electronic contacts