Job Title

ICON has opened a Local Trial Manager II positionFully remote, not travel. Position filling fast, apply today.Must currently be working for a CRO, Pharmaceutical or Biotechnology Company, have a bachelors degree with at least 5 years clinical and 3 years of trial management with a title such as Clinical Trial Manager, Local Trial Manager, Study Manager, Study Lead, Ops Manager, Local Trial Manager...Local Trial Manager IIResponsibilities: Responsible for running the US portion of global trials, working with cross functional teams, budget, and vendor oversite. Planning, management, and oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST). Supports country-level operational planning and accountable for sites election within assigned country/-ies. Contributes and develops to program/study-specific materials e.g., monitoring plan, study specific training documents. Supports and contributes to Clinical Study Teams (CSTs) / Trial Management Teams (TMTs) as applicable, agenda driven, present at meetings. Communicates country status (including timelines and deliverables) to key stakeholders (e.g., Global Clinical Managers [GCM], Program Managers, CST or TMT, Development Operations Manager [DOM] etc) with oversight as required and ensures updates to relevant systems. Accountable for site-level goal setting and study-specific deliverables for clinical sites within their country/-ies. Contributes to, deliver and/or lead CRA, Investigator and Study Coordinator training. Provides oversight and monitoring of applicable vendor activities..., laboratories and equipment provisioning. Engages with local cluster team and local functions from a study perspective (e.g., Local Medical Affairs team, DOM) Provides country level input into the Country Operational Plan (COP) and partner with the DFM through feasibility and with the GCMs to ensure local delivery of the study. Responsible for approval of Baseline and Revised Enrolment Plans (Country Level) Contributes to the study-level forecast for investigational product, support study level accountability and reconciliation across assigned countries, management of ELE (enrolment long-range estimates) process.Qualifications: Minimum 3 years experience running local/regional/global trials in a CRO, Pharmaceutical or Biotechnology environment Bachelors degree & 5 years of directly related experience