Clinical Study Coordinator Position Available In Middlesex, Massachusetts

Job Title:

Clinical Study Coordinator Job Description As a Study Coordinator, you will engage in human subject research, monitoring participants as they utilize various technology products and collecting data throughout the sessions. You will work directly with participants, ensuring proper setup and data collection during scheduled sessions that can last up to 2.5 hours each. Responsibilities Consent participants according to protocol. Take necessary vitals and measurements such as height, weight, and EKG at the beginning and throughout the session. Ensure participants are properly set up with devices and monitoring equipment. Use several pieces of instrumentation to observe participants during various activities. Ensure data monitoring is functioning properly throughout the session. Guide participants through the study. Ensure proper data collection. Essential Skills Experience in research. Proficiency in data entry. Ability to implement study protocols. Understanding of clinical research. Knowledge of study design. Additional Skills & Qualifications Experience with human subject research. Work Environment The work environment involves working directly with human subjects and using various technological devices and monitoring equipment. Sessions can last up to 2.5 hours, and the role requires attention to detail and adherence to protocols.