Bausch Health - Boise, ID
posted 2 months ago
Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing, and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future. In this role, you will lead or collaborate on required tasks prior to the commencement of clinical trials, which include clinical planning, protocol development, case report form (CRF) development, IRB submissions, investigator agreements, informed consent form (ICF) development, site selection, and communication with clinical trial sites regarding all logistics including contract agreements, support materials, and training. You will provide clinical oversight and management for clinical trials to facilitate compliance with FDA and other applicable international regulatory requirements and company standard operating procedures (SOPs) during all company clinical investigations and post-market studies. Your responsibilities will also include communicating with vendors and clinical trial sites regarding study conduct, data monitoring, and logistical management of follow-up and close-out study visits to ensure compliance with protocols and GCP requirements. You will collaborate on clinical data processing in accordance with departmental SOPs and guidelines, verify, review, and track CRFs, and generate Data Clarification Forms (DCFs) for all missing or inaccurate data. Additionally, you will assist in the evaluation and analysis of clinical trial data to facilitate completion of clinical trial reporting requirements, including report writing, clinical photo-documentation, FDA, and manuscript submissions. This position requires a Bachelor's degree in a health profession or science, along with a minimum of 5 years of ongoing clinical trials experience in the pharmaceutical or device industry. You will need to demonstrate proficiency in knowledge of GCPs and FDA regulatory requirements, as well as possess excellent verbal and written communication skills, computer proficiency, and data management experience. The role may require 10%-30% travel, and you will be expected to work independently while effectively collaborating with various teams.