Description
What you will be doing:
- Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements
- Leads or supports cross-functional trial teams, including vendors
- Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders
- Proactively identify and resolve issues that arise during trial conduct; manage escalation of trial-related issues
- Participate in or lead the development of core trial documents, trial plans and system set-up; participate in preparation and ensure operational excellence of protocol and implementation of appropriate systems, standards, and processes to ensure quality across investigative sites, vendors, and data
- Participate in or lead preparation of vendor requirements and project scope and selection of trial vendors; effectively manage interactions and escalations with vendor trial team
- Participate in or lead feasibility assessment and selection of countries and sites for trial conduct
- Participate in or facilitates site engagement and communications with investigators and/or staff to support trial milestones and deliverables
- Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top line results; participate in data reviews and review of statistical analysis plans
- Participate in or lead set-up and implementation of effective investigator and site monitor training; coordinate operational and therapeutic area training for internal and external trial team members
- Provide oversight and direction to trial team members for trial deliverables
- Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems
- Ensure quality and completeness of TMF for assigned clinical trials
- Participates in inspection readiness activities including coordination of clinical trial team deliverables
- Participate in the evaluation and implementation of patient-focused strategies for assigned trials, as applicable
- Responsible for the management of budgets, timelines and resources for assigned clinical trial responsibilities