Job Description

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

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