Overview

Clinical Research Coordinator (CRC) for busy and rapidly growing clinical research site for Phase Ib-IV studies. Pleasant working environment. General job functions include patient care, study coordination, administrative duties.

Candidate must possess the following:

· Exceptional professionalism

· Commitment to excellence and quality patient care

· Impeccable organizational skills and attention to detail

· Excellent communication and interpersonal skills to effectively interact with Principal Investigator, research team, Study Sponsor/CROs, potential subjects and referral sources

· Ethical compass that compels the candidate to be honest, detail-oriented, and self-driven

· High level critical thinking skills

· Working knowledge of medical terminology and lab collection/processing/storage procedures

· Proficiency with computers and Microsoft Office Suite

Responsibilities:

· Obtain study participant informed consent

· Execute study protocol procedures in detailed, organized, and professional manner

· Perform lab draws and processing, and package specimen shipments

· Complete study source documents and adverse event reporting

· Maintain study-specific files and supplies

· Communicate with Study Sponsor/CRO regarding study-specific questions

· Participate in site visits from Sponsors/CROs, including site initiation and monitoring visits

Job Type:

· Full-time (non-exempt)

Requirements:

· Two (2) or more years of experience as CRC

· Bilingual (Spanish) is a plus

· Clear understanding of ICH, FDA, and GCP regulations

· Must be willing to travel (<5%) to participate in Investigator meetings