What are the responsibilities and job description for the Clinical Research Coordinator position at Evolution Research Group?
Job Description
Job Description
About Company : Who is ERG?
ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with an expertise in early and late-stage neuroscience drug development. With 19 wholly owned clinical sites and 5 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 340 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.
About the Role :
As a Clinical Research Coordinator at ECT-Endeavor Clinical Trials LLC, you will play a crucial role in the successful execution of clinical trials. You will be responsible for coordinating and managing the day-to-day activities of clinical research studies, ensuring compliance with study protocols, and maintaining accurate and complete study documentation. Your attention to detail and ability to work collaboratively with study teams will be essential to the success of the trials. You will have the opportunity to work with cutting-edge medical technologies and contribute to the development of new treatments and therapies.
Minimum Qualifications :
- Candidates must have a Bachelor's degree in a related field, or an Associate’s degree with relevant clinical research experience. Alternatively, years of experience in clinical research may be considered in lieu of formal education.
- 1 years of experience in clinical research coordination
- Knowledge of FDA regulations and ICH guidelines
- Excellent organizational and communication skills
- Ability to work independently and as part of a team
Preferred Qualifications :
Responsibilities :
Skills :
As a Clinical Research Coordinator I, you will utilize your strong organizational and communication skills to manage the day-to-day activities of clinical research studies. Your attention to detail and ability to work collaboratively with study teams will be essential to ensuring compliance with study protocols and maintaining accurate and complete study documentation. You will also utilize your knowledge of FDA regulations and ICH guidelines to ensure the successful execution of trials. Additionally, your experience with electronic data capture systems, clinical trial management systems, and patient recruitment and retention will be beneficial in this role.
