Clinical Trial Associate

Role: Clinical Trial Associate supporting daily activities for investigative studies at CRISPR Therapeutics, primarily focusing on trial documentation, data tracking, and regulatory compliance. Responsibilities: maintain eTMF, coordinate study meetings, manage study samples and vendor relationships, oversee documentation version control, support clinical supply processes, and contribute to process improvements. Qualifications: BS/BA with 1-3+ years in clinical research; knowledge of GCP, CFR, and clinical documentation; proficiency in MS Office; strong organizational and communication skills. Preferred: experience with CROs, global studies, IND/CTA submissions, and drug development processes. HighValue: early to mid-phase (likely Ph I-II) gene therapy trials in hemoglobinopathies or related indications, with focus on clinical operations, document management, and regulatory compliance. WorkSetup: hybrid (onsite in Boston with flexible remote options), with a collaborative environment emphasizing cross-functional teamwork and process development.