Research Coordinator

UNC-Chapel Hill•Chapel Hill, NC

2d•Hybrid

About The Position

THIS IS A TIME - LIMITED POSITION WITH AN ESTIMATED DURATION OF 2 YEARS . The Research Coordinator will serve to manage projects for large multi-institutional clinical trials. Responsibilities include cohesive efforts in planning, organizing, implementing, and managing study processes. This position will oversee day-to-day operations and coordination of projects, including facilitating meetings, coordinating study start-up activities, and tracking program progress. This position must be adaptive in nature, requiring a broad skill set and the ability to quickly address operational opportunities and weaknesses which may require interacting with multiple state and federal entities. In addition, this position ensures timely updates and formatting consistency to relevant reports and websites; compliance for quality assurance to include identifying, tracking, and reporting any barriers to hinder a successful outcome; deliverables for project protocols across various participating sites, vendors, and institutions are met; and all research is in adherence with the FDA Code of Federal Regulations, ‘Good Clinical Practices’, and IRB regulations for the protection of human subjects. Communication is critical as this position will manage communication with various levels of stakeholders to ensure accuracy and conclusiveness. This position will also work closely with senior leadership to determine necessary implementation and streamlined processes for expansion and operations.

Requirements

Adaptive nature with a broad skill set.
Ability to quickly address operational opportunities and weaknesses.
Familiarity with state and federal entities.
Knowledge of FDA Code of Federal Regulations, ‘Good Clinical Practices’, and IRB regulations.
Strong communication skills.
Ability to manage communication with various levels of stakeholders.

Responsibilities

Oversee day-to-day operations and coordination of projects.
Facilitate meetings.
Coordinate study start-up activities.
Track program progress.
Address operational opportunities and weaknesses.
Ensure timely updates and formatting consistency to relevant reports and websites.
Ensure compliance for quality assurance, including identifying, tracking, and reporting any barriers to a successful outcome.
Ensure deliverables for project protocols across various participating sites, vendors, and institutions are met.
Ensure all research is in adherence with the FDA Code of Federal Regulations, ‘Good Clinical Practices’, and IRB regulations for the protection of human subjects.
Manage communication with various levels of stakeholders to ensure accuracy and conclusiveness.
Work closely with senior leadership to determine necessary implementation and streamlined processes for expansion and operations.