What are the responsibilities and job description for the Clinical Research Coordinator position at RETINA GROUP OF NEW ENGLAND, P.C?
Company Description The Yale School of Medicine, founded in 1810, is a globally recognized center for biomedical research, education, and advanced health care. It includes one of the nation’s oldest schools of public health, the internationally recognized Child Study Center, and the Yale Cancer Center, a National Cancer Institute-designated comprehensive cancer center. The school is closely affiliated with major institutions such as Yale-New Haven Hospital, the Connecticut Mental Health Center, Pierce Laboratory, and the VA Connecticut Healthcare System. Yale School of Medicine is consistently among the leading recipients of research funding from the National Institutes of Health and other organizations, and is a member of the AAMC and AAHC. Its distinctive curriculum emphasizes small-group learning, independent thinking, and original research, with all students completing a thesis prior to graduation.
Role Description This full-time, on-site Clinical Research Coordinator role is based in New York, NY. The coordinator will support clinical trials and research studies by managing participant recruitment, screening, and enrollment, and by obtaining and documenting informed consent in accordance with regulatory and ethical standards. Day-to-day responsibilities include coordinating study visits, collecting and entering clinical data, maintaining accurate study records, and ensuring adherence to approved protocols and institutional policies. The role also involves collaborating with investigators, research nurses, and other team members, preparing regulatory submissions, and assisting in reporting adverse events or protocol deviations. The coordinator will help maintain study timelines, support monitoring and auditing activities, and contribute to the overall quality and integrity of clinical research projects.
Qualifications
Role Description This full-time, on-site Clinical Research Coordinator role is based in New York, NY. The coordinator will support clinical trials and research studies by managing participant recruitment, screening, and enrollment, and by obtaining and documenting informed consent in accordance with regulatory and ethical standards. Day-to-day responsibilities include coordinating study visits, collecting and entering clinical data, maintaining accurate study records, and ensuring adherence to approved protocols and institutional policies. The role also involves collaborating with investigators, research nurses, and other team members, preparing regulatory submissions, and assisting in reporting adverse events or protocol deviations. The coordinator will help maintain study timelines, support monitoring and auditing activities, and contribute to the overall quality and integrity of clinical research projects.
Qualifications
- Demonstrated experience in clinical research and clinical trials, including coordination of study activities and participant follow-up.
- Strong knowledge of research protocols and study procedures, with the ability to implement and monitor protocol compliance.
- Proficiency in obtaining and documenting informed consent, with a clear understanding of ethical and regulatory requirements.
- Applied research skills, including data collection, documentation, and use of electronic data capture or clinical trial management systems.
- Bachelor’s degree in a relevant field (e.g., life sciences, public health, psychology, nursing) or equivalent education and experience.
- Familiarity with Good Clinical Practice (GCP), institutional review board (IRB) processes, and applicable regulatory guidelines.
- Strong organizational skills, attention to detail, and ability to manage multiple studies or tasks simultaneously.
- Effective interpersonal and communication skills for working with participants, investigators, and multidisciplinary teams.
- Ability to work on-site in New York, NY and adhere to institutional policies, including any occupational health and safety requirements.
- Prior experience in an academic medical center or hospital-based research environment is beneficial.