RCI-ABBV-33750 Clinical Study Coordinator (Part Time) (Clinical Research/Clinical Trials/Clinical Studies/IRB Submission)

Responsibilities

• •This role will support management and operationalization of exploratory and clinical studies conducted at the Eye Care Research Center according to the study protocol, regulatory requirements, and standard operating procedures (SOPs)
• •The role will support the recruitment, scheduling, and execution of subject visits as well as creation of source documents
• •The role will collect, enter, and maintain accurate study data, ensuring timely reporting of data to necessary stakeholders
• •Role works closely with the clinical team and ECRC personnel to support smooth study execution
• •Project manager will support development, authoring and maintenance of SOPs and work instructions
• •This role is responsible for data entry, cleaning, and maintenance of test material, inventory, supplies, and equipment
• •Supports execution of clinical research studies, responsible for overall conduct of clinical studies and operational activities at the site
• •Recruit, screen, enroll, consent study subjects as delegated by investigator(s)
• •Perform study specific assessments as delegated by investigator(s)
• •Perform data collection and
• •Maintain ECRC inventory and equipment
• •Support ongoing development and maintenance of standard operating procedures and work instructions for the site, including general ECRC operations processes
• •9 more items(s)