Company Description
Cardiovascular Medical Group of Southern California (CVMG) is an academic medical practice specializing in cardiology and internal medicine, with a commitment to personalized patient care. Patients are paired with a dedicated cardiologist, supported by in-house sub-specialists and advanced technology. CVMG is affiliated with prestigious medical institutions, including Cedars-Sinai Medical Center. The group is dedicated to delivering high-quality care backed by cutting-edge research and expertise.
Role Description
This is a full-time, on-site role for a Clinical Research Coordinator II, based in Beverly Hills, CA. The Clinical Research Coordinator II will manage all aspects of clinical trials, including participant recruitment, obtaining informed consent, and coordinating with research teams. Responsibilities also include ensuring compliance with study protocols, maintaining accurate documentation, collecting and entering data, and liaising with investigators and sponsors to support successful outcomes.
Schedules and participates in monitoring and auditing activities. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
Notifies direct supervisor about concerns regarding data quality and study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Maintains research practices using Good Clinical Practice (GCP) guidelines.
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
Qualifications
· Strong knowledge of obtaining Informed Consent and ensuring compliance with ethical standards
· Understanding and experience in implementing study Protocols within clinical settings
· Hands-on experience in Research and Clinical Research, with a thorough understanding of methodologies
· Experience in managing Clinical Trials, including recruitment, coordination, and data monitoring
· Ability to work collaboratively within a team while managing multiple projects
· Strong organizational, analytical, and problem-solving skills
· Proficiency in maintaining accurate and comprehensive documentation
· Bachelor's Degree in a related field, with preference for candidates who have experience in cardiovascular research
· 5 years Clinical research related experience required