Research Assistant (Clinical)- temporary role

KEY RESPONSIBILITIES CLINICAL & PATIENT‑FACING DUTIES - Obtain and document vital signs (blood pressure, heart rate, temperature, respiratory rate, height, weight) per protocol - Perform venipuncture and blood draws for research studies - Process, label, centrifuge, store, and ship laboratory specimens according to protocol and laboratory manuals - Perform 12‑lead ECGs and ensure accurate transmission and documentation - Prepare exam rooms and maintain clinical supplies for study visits - Assist with participant flow during research visits and ensure patient comfort and safety RESEARCH & DATA RESPONSIBILITIES - Accurately enter clinical and study data into electronic data capture (EDC) systems and/or study databases - Maintain source documentation that is complete, accurate, and audit‑ready - Assist with informed consent discussions and documentation, as directed - Support study visits, screenings, and follow‑ups according to protocol schedules - Identify and promptly report protocol deviations, adverse events, and data discrepancies to the study team COMPLIANCE & OPERATIONS - Follow GCP, IRB, HIPAA, and institutional policies - Assist with study regulatory binders and document maintenance - Participate in monitoring visits, audits, and inspections as needed - Maintain required certifications and training REQUIRED QUALIFICATIONS - Hands‑on clinical experience performing: - Vital signs - Venipuncture / blood draws - Laboratory specimen processing - ECGs - High school diploma or equivalent required; Associate’s or Bachelor’s degree in health sciences, life sciences, or related field preferred - Prior experience in clinical research, healthcare, or medical assistant roles - Strong attention to detail and documentation accuracy - Basic computer proficiency and data entry experience - Ability to work independently and as part of a multidisciplinary team PREFERRED QUALIFICATIONS - Medical Assistant certification (CMA, RMA, or equivalent) - GCP certification - Experience with EDC/eSource systems (e.g., CRIO, Medidata) - Prior experience in industry‑sponsored clinical trials - Phlebotomy certification PHYSICAL & WORK REQUIREMENTS - Ability to stand, walk, and perform clinical procedures for extended periods - Ability to lift and move supplies (up to 25 lbs) - Comfortable working in a fast‑paced clinical environment