Research Assistant

The Research Assistant I is responsible for performing clinical research procedures in accordance with study protocols while ensuring participant safety, protocol compliance, and high-quality patient care. This role supports the successful execution of clinical studies by completing protocol‑specific procedures, maintaining accurate documentation, and providing an exceptional participant experience. Ensure the safety, well‑being, and comfort of study participants throughout all study activities. Monitor participants for adverse events and promptly intervene, document, and report findings according to study protocols. Adhere to protocol‑specific schedules and required study timelines. Perform clinical procedures as outlined in study protocols, including: Vital signs Electrocardiograms (ECGs/EKGs) Physiological measurements Meal distribution and participant monitoring Preparation of study supplies and equipment Perform technical procedures within the scope of training and certification, including: Venipuncture and blood collection Medication administration (when authorized) Explain informed consent documents to study participants and ensure consent is obtained, understood, and properly documented prior to study participation. Maintain adequate inventory of study supplies and equipment to support daily clinical operations. Accurately document study activities in accordance with Good Clinical Practice (GCP), study protocols, and applicable regulatory requirements. Provide professional, compassionate, and high‑quality customer service to study participants. Collaborate effectively with investigators, clinical staff, and study teams. Perform additional clinical and research‑related duties as assigned. Qualifications Required High school diploma or equivalent required. One of the following certifications: Certified Medical Assistant (CMA) Registered Medical Assistant (RMA) Other comparable healthcare certification may be considered. Current CPR/BLS certification (or ability to obtain upon hire). Experience performing venipuncture, vital signs, and ECG/EKGs. Strong communication and interpersonal skills. Basic computer proficiency and experience with electronic documentation systems. Ability to work in a fast‑paced clinical research environment while maintaining attention to detail. Preferred Previous experience in clinical research or clinical trial operations. Experience with informed consent procedures. Knowledge of Good Clinical Practice (ICH‑GCP) guidelines. Experience using electronic medical records (EMR), electronic data capture (EDC), or clinical trial management systems (CTMS). Physical Requirements Ability to stand and walk for extended periods. Ability to lift and move up to 25 pounds. Manual dexterity to perform clinical procedures. Ability to work flexible schedules, including early mornings, evenings, weekends, or holidays, based on study requirements. #J-18808-Ljbffr