About this role
Clinical Trial Operations Specialist at Iqvia. Location: Durham or United States. Role: coordinating trials, maintaining documentation, managing systems Requirements: University degree or comparable education and 3+ years clinical trial operations/project coordination experience; GCP/ICH knowledge, strong communication, organization, and MS Office proficiency. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office Commitment: Full Time Workplace: Remote Languages: English