Sr. Associate, Clinical Data Operations

Role: Senior Clinical Data Operations Associate supporting bio/pharma and academic clinical trials; focuses on sample tracking, data management, and operational support. Responsibilities: manage study documentation, monitor sample processing and reporting, oversee query resolution, ensure data quality and compliance with GxP, HIPAA, and GCP standards, coordinate sample return/destruction, and contribute to process improvement and training. Collaborates cross-functionally with Bioinformatics, Data Management, Clinical Operations, and Technology teams. Qualifications: Bachelor's in a scientific field or equivalent, with 1+ years of experience; preferred 4+ years, with knowledge of oncology, molecular biology, genetics, or bioinformatics. Skills include advanced data QC, programming basics, process implementation, and strong communication. Experience in GCP, study documentation, and cross-team collaboration is valued. Work setup primarily remote in Boston; other details on travel are not specified.