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.