Research Assistant

Role Description: Immediate Hire Assist in Phase II–IV cardiology clinical trials from start-up through close-out, ensuring strict protocol adherence and accurate study execution. Identify, recruit, and screen potential participants through EMR review, conduct study visits, and manage ongoing patient follow-up. Perform ECGs and protocol-required blood draws, enter data accurately and in a timely manner into EDC systems, and respond promptly to sponsor and CRO data queries. Maintain organized, regulatory-compliant, audit-ready study documentation while collaborating effectively with investigators, sponsors, CROs, and clinical staff.

Qualifications: Knowledge of Informed Consent and Protocol documentation procedures Exceptional organizational, communication, and problem-solving skills Bachelor’s degree in a related scientific field or equivalent clinical research experience Previous experience working with diverse therapeutic areas or in a multi-specialty setting is advantageous. Bachelor’s degree in Life Sciences, Nursing, Public Health, or related field or working on a degree Bilingual is a plus