What are the responsibilities and job description for the Clinical Research Coordinator position at Evolution Research Group?
Job Description
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 :
Additional Responsibilities :
Skills and Qualifications :
