IP Coordinator - Unmasked Research

Colorado Retina Associates is looking for a IP Coordinator Unmasked! Colorado Retina Associates is the premier retina practice of the Rocky Mountain region.

Come join a team that strives to provide advanced care and cutting-edge therapies for our patients.

Just as we aim to have top notch patient care, we aim to take great care of our team members by providing competitive salary & benefits, continuing education and advancement programs, and an opportunity to work with the top-ranked retina specialists in the US with state-of-the-art equipment and retina treatment methods.

JOB TYPE/COMPENSATION: Full TimeClinical ResearchBase Wage: $50,369.73 - $80,591.56 (based on education and experience) Position Summary: The unmasked research coordinator is primarily responsible for coordinating research patient treatment visits according to both the International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines and the Institutional Review Board (IRB) approved study protocol and/or manual of procedures.

Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.

Role and Responsibilities: IP Coordinator Level I: Conduct unmasked monitoring visits Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study for unmasked purposes Works with team member responsible for ordering study or ancillary supplies to ensure adequate inventory is on hand Ensures study staff is properly trained on study-related information (i.e.

protocol, Informed Consent Form (ICF), manuals, etc.), aseptic and sterile field technique, and ensures the training is documented Reviews and comprehends all study protocols and procedure/pharmacy manuals Efficiently completes all study tasks delegated to them (i.e.

scribing, Intraocular pressure [IOP], etc.) Manage of unmasked RAs (if applicable) Collects updated adverse events and serious adverse events that need to be reported to the sponsor and IRB within required timeframe per the protocol and in accordance with RCA Standard Operating Procedure (SOP) Answer any unmasked study-related questions from subject Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract (if applicable)15AUG2025 3 Oversees data and ensures that it is being entered correctly and resolves any queries issued within required timeframe (if applicable) Collects and reports ALL Adverse Events in a masked fashion Collects and reports ALL Serious Adverse Events in a masked fashion Subject safety check-in calls Works with the monitor to make any corrections needed to meet requirements and deadlines as needed Obtain any applicable additional/required sponsor training and/or certifications Education and Experience: High School Diploma ...