Research Coordinator Jobs

About The Position

Requirements

• Bachelor's Degree Required or equivalent combination of experience, education and or certifications.
• Background checks, pre-employment health screenings, and drug screenings will be conducted on all new hires prior to employment.
• This position will not consider candidates who require immigration sponsorship now or in the future.

Nice To Haves

• Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.

Responsibilities

• Work closely with Principal Investigators and other study team members on all clinical research projects assigned.
• Demonstrate a working knowledge of the regulatory framework for FDA and non-FDA regulated studies.
• Facilitate and / or complete activities required for study start-up including regulatory submissions and other aspects required for site initiation.
• Coordinate multiple clinical trials or research projects simultaneously.
• Manage ongoing clinical trial conduct from enrollment to follow up visits, data management, safety reporting and compliance oversight.
• Prepare and submit regulatory documentation to the IRB such as: personnel changes, annual protocol continuations, protocol modifications, adverse event reports, unanticipated events.
• Demonstrate proficiency with the various electronic platforms utilized in clinical research such as: IRB Pro, Protocol Builder, CRConnect, OnCore, e-regulatory platforms and Epic.