Clinical Trials Associate
Monte Rosa Therapeutics, Inc.
Role: Clinical Operations Associate supporting trial planning, start-up, maintenance, and closeout activities within a biotech setting. Responsibilities: develop study documents (protocols, ICFs, IBs) liaise with investigators and site staff to foster sponsor-site relationships review regulatory packets monitor data quality manage biological sample logistics support meeting coordination track IMP supplies oversee TMF submissions with CROs Also assists with study finance, vendor invoicing, and process improvements. Requirements: BA/BS with at least 2 years of experience in clinical research at investigator sites, CROs, or sponsors strong knowledge of ICH/GCP and FDA regulations effective communication and organizational skills experience with eTMFs preferred. High-Value: clinical trial support regulatory compliance sample management TMF oversight cross-functional collaboration biotech environment protocol development trial logistics. #J-18808-Ljbffr Monte Rosa Therapeutics, Inc.
Vacancy posted 14 hours ago
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