3 jobs found in Pearl River

ROLE SUMMARY: The Clinician Medical Monitor (CMM) is accountable for providing medical and scientific expertise and oversight for Global Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies to ensure patient safety. Additional study level activities include presentation of study results to internal and external committees or advisory boards, presentation of data at international scientific meetings and publication of study results in peer reviewed journals. The CMM will also act as a medical monitor for select clinical trials, including phase 2B and phase 3 registration studies, The CMM is accountable for patient safety for subjects participating in Pfizer clinical trials and provides medical guidance during the design, execution, and reporting for clinical studies. In addition to study level activities, the CMM will participate in program level activities including...

ROLE SUMMARY The clinician medical monitor may contribute towards providing medical and scientific expertise and oversight for Clinical Trials. The clinician medical monitor may be required to design a development strategy for multiple protocols designed to obtain worldwide approval for a compound or group of compounds. The clinician will work also collaboratively with members of clinical development teams across studies and across the Pfizer enterprise on digital health technologies and digital endpoint development ROLE RESPONSIBILITIES Develop plans for implementation, validation, and/or qualification of digital health technologies into clinical development programs and clinical trials Accountable for the design of protocols, clinical reports, clinical portions of regulatory submissions, protocol amendments and conducts data review, analysis, and interpretation of data from studies. Accountable for safety across the study: Provide study team with...

ROLE SUMMARY The clinician medical monitor is a member of an energetic team working on an innovative RSV candidate vaccine and is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design, execution, monitoring, delivery and reporting of one or more clinical studies and to ensure patient safety. In addition to study level activities, the clinician medical monitor will participate in standing committees, review compounds for potential in-licensing, including performance of due diligence reviews, and provide assistance to new business development on market opportunities and the target product profile. ROLE RESPONSIBILITIES   Accountable for safety across the study: Provide study team with medical advice for all medical issues during risk assessment and mitigation planning to enable quality, compliance and patient safety at the trial, site and patient level. Ensures...