Clinical Research Coordinator I

Rochester Regional Health

7d•$54,800 - $63,400•Onsite

About The Position

Conducts and assists in the System physician and staff’s clinical research trials and projects. Obtains informed consent, collects, maintains, and processes study information and research data in strict accordance with specified research and clinical protocol.

Requirements

Bachelor’s Degree in biology or healthcare related field
Excellent time management skills with the ability to manipulate multiple schedules
Ability to comprehend and utilize information from multiple sources to support the identification and recruitment of potential research participants based on strict study criteria
Ability to communicate and work professionally with all levels of health care providers (physicians, nursing staff, laboratory, practice managers etc.)
High level of attention to detail and thoroughness
Self-starter and motivated
Ability to work independently as well as in a team setting
Proficiency in Microsoft Office Suite
Able to sit and work at a computer keyboard for extended periods of time.
Ability to effectively communicate both orally and in writing.
Occasional stooping, bending, reaching, lifting and pushing up to 20 pounds.
Close visual acuity, read charts, analyze and prepare data, transcribing, viewing a computer screen, dials, equipment settings, literature and other printed or handwritten materials.
Work with equipment and manipulate equipment settings, computer keyboard, etc.
OSHA Category II: Some risk of exposure to blood/body fluids in the day to day job duties.
Regular and on-time attendance.
Occasional travel by conventional means to other locations as required.
Must hold valid driver’s license
Must be eligible to live and work in the US

Nice To Haves

ACRP or SOCRA certification
1-3 years of experience in healthcare or related science field, with knowledge of medical terminology
Comfortable traveling to various clinical sites with the St. Lawrence Health System
Occasional travel for conferences and/or investigator meetings may be required as needed

Responsibilities

Obtains informed consent
Collects, maintains, and processes study information and research data in strict accordance with specified research and clinical protocol
Prepare and facilitate site selection, initiation, monitoring, and close-out visits conducted by sponsor pharmaceutical companies, and follow-up as necessary
Attend subject study visits
Document and record accurate data in compliance with the protocol and study design in a timely and efficient manner
Identify and recruit potential research participants based on strict study criteria