Job Description

Employer Industry: Healthcare Research Why consider this job opportunity: Salary up to $34.81/hour Opportunity for career advancement and professional growth within the organization Comprehensive benefits package, including recognition programs Remote work flexibility, allowing you to work from anywhere Chance to be part of a mission-driven organization focused on patient care and research What to Expect (Job Responsibilities): Monitor and maintain compliance with applicable regulations and institutional policies related to clinical research Prepare, review, and submit regulatory documentation necessary for clinical trials Facilitate the submission of study protocols and related documents to the Institutional Review Board (IRB) Maintain accurate regulatory documentation, including informed consent forms and safety reports Act as a liaison between the research team, principal investigators, sponsors, and regulatory authorities What is Required (Qualifications): Bachelor's Degree in Healthcare Management or a related field required 2-3 years of regulatory affairs experience required Familiarity with Good Clinical Practice (GCP) guidelines and relevant regulations Strong organizational skills with attention to detail and ability to manage multiple projects Excellent written and verbal communication skills How to Stand Out (Preferred Qualifications): Proficiency in using relevant software and electronic systems for regulatory documentation management Understanding of the clinical trial process and importance of regulatory compliance We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. #J-18808-Ljbffr Mass General Brigham

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