Clinical Research Coordinator
Company: Evolution Research Group
Location: Staten Island
Posted on: April 2, 2026
|
|
|
Job Description:
Title: Clinical Research Coordinator, Psych exp. preferred
Location: Staten Island, NY About us: ERG is a leading U.S. based,
privately held, independent clinical research site company, and
provider of clinical development services with expertise in early
and late-stage neuroscience drug development. With 20 wholly owned
clinical sites and 4 affiliated sites, we conduct in-patient and
out-patient phase I-IV clinical research studies. ERG has 400
in-patient beds, a large and growing database of patients suffering
from mental illness, neurological disorders, sleep disorders,
addictions, Acute and Chronic Pain, diabetes, and other illnesses
as well as normal healthy volunteers who participate in trials for
the advancement of medicine. With access to over 32 million
patients/subjects and 5000 completed trials, ERG continues to grow
its capabilities and expand into indications where there are
tremendous unmet medical needs in the United States and globally.
Job Description: The Clinical Research Coordinator is responsible
for the overall coordination, organization, management, and
efficient implementation of clinical trials. The CRC completes all
study related procedures and distributes study medication and
instructions to research subjects under the direction of the
Principal Investigator and the Site Director. They maintain
accurate, confidential files and documentation of study
participants. In executing these position responsibilities, the
Clinical Research Coordinator is guided by FDA regulations, Good
Clinical Practice (GCP), and company standard operating procedures
and policies. Responsibilities: General: Obtain detailed knowledge
of study protocols by reviewing with Principal Investigator (PI)
and Site Director. Assist in drafting and reviewing source
documents for accuracy before study start-up. Collaborate with PI
and Site Director to clarify study components as needed. Manage
studies under the guidance of PI and Site Director to ensure
protocol compliance. Study Management: Perform delegated study
activities under Site Director’s supervision. Attend investigator
meetings as directed. Ensure protocol adherence and report breaches
to sponsors and regulatory bodies. Screen, enroll subjects,
schedule visits, and document communications. Assist PI in
maintaining data integrity and subject safety. Enter study data
(paper or electronic) and track adverse events. Conduct study
close-out procedures. Additional Responsibilities: Take on evolving
tasks as required by the organization. Skills and Qualifications:
High School Diploma required; college degree preferred. 2-4 years
of experience or Clinical Research Coordinator certification.
Strong communication, medical terminology knowledge, and
problem-solving skills. Familiarity with GCP, ICH guidelines, and
regulatory requirements. Proficient in Word, Excel, and clinical
research software.
Keywords: Evolution Research Group, Jersey City , Clinical Research Coordinator, Science, Research & Development , Staten Island, New Jersey
