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.