Clinical Research Coordinator

The ideal candidate will have patient-facing experience and at least 1 year of experience as a study coordinator in a clinical trial setting. Phlebotomy training/experience, laboratory sample processing experience, and ECG training are strongly preferred. Responsibilities: Coordinate and oversee clinical research studies in accordance with protocols and regulatory requirements. Recruit, screen, and enroll eligible participants for studies. Obtain informed consent from participants and maintain documentation. Perform or assist with clinical procedures, such as phlebotomy, ECGs, and laboratory sample processing. Collect, record, and maintain study data and source documents. Communicate effectively with study sponsors, investigators, and study team members. Ensure compliance with study protocols, regulations, and institutional policies. Participate in study meetings, trainings, and audits as required. Qualifications: Bachelor's degree in a health-related field or equivalent experience. Minimum of 1 year of experience as a study coordinator in a clinical trial setting. Patient-facing experience/background is essential. Phlebotomy training/experience is strongly preferred. Laboratory sample processing experience is strongly preferred. Trained to perform ECGs is strongly preferred. Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements. Excellent communication, organization, and interpersonal skills. Ability to work independently and as part of a team. Detail-oriented with strong problem-solving skills.