TruMinds Clinical

Conduct site visits, ensure regulatory compliance, verify source documents, support study start-up tasks, and prepare monitoring reports. | Bachelor’s degree in Life Sciences, 2-4 years clinical research experience including site monitoring, mandatory medical device experience, strong FDA and GCP knowledge, and proficiency in Microsoft Office. | We are looking for a “Clinical Research Associate (CRA)” to join one of our Fortune 500 clients. Job Summary Conduct site qualification, initiation, monitoring, and close-out visits Ensure compliance with protocols, GCP, and regulatory requirements Perform source document verification and data query resolution Support start-up tasks such as protocol development and site contracts Maintain study documentation and monitor investigational product inventory Prepare monitoring visit reports and follow-up letters Qualifications: Bachelor’s degree in Life Sciences or related field (Medical Technology preferred) 2–4 years of clinical research experience, including site monitoring Strong understanding of FDA regulations and GCP Experience with medical devices or in vitro diagnostics (IVDs) preferred Excellent communication, organizational, and time management skills Proficient in Microsoft Office Suite Job Type: Contract Pay: $30.00 - $40.00 per hour Expected hours: 40 per week Application Question(s): • Medical Device experience is mandatory Ability to Commute: • Boston, MA 02108 (Required) Ability to Relocate: • Boston, MA 02108: Relocate before starting work (Required) Work Location: In person