Clinical Research Coordinator 1-3; Brain Institute

UVA Health•Charlottesville, VA

2d•Onsite

About The Position

The UVA Brain Institute is seeking candidates for a Clinical Research Coordinator (CRC) 1, 2, or 3, Licensed or non-Licensed, to join our growing team. The Clinical Research roles are ideal for individuals with some clinical research experience or those looking to begin a rewarding career in clinical research. In this position, you will work with an experienced CRC and/or Principal Investigator on a variety of research projects across multiple neuroscience-related disciplines. Our research team conducts a variety of investigator-initiated studies and also supports federally funded and industry clinical research. Nearly all studies require the collection, processing, and shipment of biospecimens. We actively collaborate with faculty members across Grounds; therefore, this role may offer the opportunity to work with investigators from a variety of schools and departments. Applicants must demonstrate excellent written and oral communication skills, attention to detail, and should have the ability to be flexible, adaptable, and resourceful in the workplace. The ideal candidate for this role will have strong problem-solving skills.

Requirements

Bachelor's Degree Required or equivalent combination of experience, education and or certifications.
For CRC 2: At least one year of clinical research experience.
For CRC 3: Minimum of 3 years of clinical research experience required.
For CRC 3: Master’s degree may substitute for 1 year of clinical research experience.
MUST be licensed to Practice in Clinical Profession such as (but not limited to): Registered Nurse, Athletic Training, Pharmacology, Medical Technology, Physical Therapy, Registered Respiratory Therapy.
For CRC 3 licensed: A minimum of 3 years of clinical research experience required.
For CRC 3 licensed: Master’s or advanced degree may substitute for 1 year of clinical research experience.
Excellent written and oral communication skills.
Attention to detail.
Ability to be flexible, adaptable, and resourceful in the workplace.
Strong problem-solving skills.

Nice To Haves

Some experience in a healthcare setting and/or knowledge of medical terminology is preferred.
Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is preferred at the time of hire and is required within one year.
Clinical Research Coordinator (CCRC) and/or Certified Clinical Research Professional (CCRP) is required within one year of hire.

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.