Erin Brady Email & Phone Number

Ravenel, SC, US

Charleston, South Carolina, United States

As a MSL, I focus on developing and maintaining peer-to-peer relationships with key medical experts in the various therapeutic areas where complement inhibition is indicated, with current focus on Ophthalmology/Retina. I collaborate with physicians and research medical experts to support trial enrollment, provide program and protocol training and ensure.

Charleston, South Carolina Area

As a MSL, I focus on developing and maintaining peer-to-peer relationships with key medical experts in the various therapeutic areas where complement inhibition is indicated. I collaborate with physicians and research medical experts to support trial enrollment, provide program and protocol training and ensure that patients, physicians, and partnered.

Charleston, South Carolina Area

Active engagement with customers across multiple market segments driving successful implementation of a new and innovative medical device. Continued relationship management and customer support throughout all stages of clinical use of BrainScope devices.

Short term contract to provide industry experience to aid in product development. Direct interaction with customers to develop relationships and demonstrate how Trials.ai trial execution platform would support their clinical trial needs.

Louisville, Kentucky Area

Active engagement of clinical research sites within a 7-state territory to find, evaluate, and select the best sites possible to run clinical research trials. Ongoing relationship maintenance between site and sponsor. Responsible for multiple therapeutic areas, including bone, muscle, & joint, cardiovascular, immunology, pain, neurodegeneration, nephrology.

Indianapolis, Indiana Area

Pharmaceutical Clinical Trial Manager supporting the Lilly Venture, running and overseeing Diabetes Phase II-IV trials. Managed study development process, arranged and participated in protocol development, coordinated/oversaw site selection, developed and adhered to trial timeline, coordinated multiple clinical trial trainings for over 100 participants.

Indianapolis, Indiana Area

Global clinical trial level project management for Urology/Men’s Health Phase III pharmaceutical trials resulting in early delivery of all trial milestones with high quality. Managed study development process, arranged and participated in protocol development, coordinated/oversaw site selection, developed and adhered to trial timeline, coordinated clinical.

Louisville, KY

Provided oversight and management of multiple clinical trials simultaneously (both as primary and back-up coordinator). Maintained regulatory documentation and patient care source documentation. Supported technical aspects for the entire office, including installation of an electronic scheduling and communication tool for all employees. Developed Phase I.

Louisville, Kentucky

Bedside nursing in a Pediatric Intensive Care Unit