Central Monitoring Manager
hace 3 semanas
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Performs the Central monitoring activities for multiple studies and ensures accurate tracking and status reporting of studies in their remit. Manage portfolio of studies for a customer and act as a customer point of contact Collaborates in the development of Central Monitoring proposal text and review of costing, contributes to proposal strategy and development. Collaborates in the development of sponsor presentations/bid defense support. Oversees at a study/customer level the appropriate tracking, interpretation, and application of data to proactively manage risk. Ensures that tracking and status reporting are performed in a timely and accurate manner. Applies data to recommend any required changes. Leads, plans, prepares, conducts, and follows up the central monitoring (Site, subject & study level review as applicable) activities and supports less experienced team members. Supports PMO in preparation of initial Risk Management Register and may prepare, distribute, and follow up Study Risk Impact Reports and coordinate Site Risk Weighting. Ensures Critical Data & Process Definition are implemented in EDC design by Data Expert. Conducts Site Risk Assessment across multiple studies, works with study start up team members, reviews site outreach, Pre-Study Visit reports and Site Risk Assessment. Prepares site risk stratifications and proposes baseline site risk levels and initial site monitoring intervention levels. Develops and establishes requirements including prescriptive risk factor mitigation strategies, SDV strategy, study-specific risk factor definition, variable Risk Factor trigger levels. Develop the Central Monitoring and other applicable plans and any subsequent changes. Manages configuration of tools, risk factors trigger levels, programming of study specific risk factors and central monitoring parameters and performs user acceptance testing of applicable tools. Performs ongoing dashboard reviews, prepares, and recommends mitigation actions and reviews recommended monitoring levels with project team and ensures that identified issues are followed to resolution. Agrees potential changes to monitoring intervention level with project team in line with the applicable plans and escalates appropriately. Performs subject clinical reviews and take appropriate actions as applicable. Performs study analytics reviews as per the applicable plans and communicates the findings appropriately. Reviews and Approves changes to monitoring levels, ensuring compliance with applicable Plans and sponsor needs are met. Oversees Project Quality and Risk Reports to ensure client satisfaction and compliance. Coaches assigned project teams internally and externally to increase the central monitoring competence. Contributes to the development and maintenance of processes, including SOP writing, process mapping and process improvements using Six Sigma and LEAN methodologies. Evaluates and collates process improvement suggestions and submits to leadership. Evaluates and submits ideas and justification for improved systems and tools to leadership.Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
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