Manager, Evidence Generation Operations Enablement (non-site based)
Core
Manages non-site-based study operations support across intake, triage, documentation, close-out, fair market value (FMV) support, and contracting for evidence generation workflows.
Role type
Manager, Evidence Generation Operations Enablement
Builds
Operational execution for evidence generation, collaborative research, and investigator-initiated studies.
Domain
Biopharmaceutical / Clinical Research Operations
Required skills
Study operations management, intake and triage, documentation tracking, study close-out procedures, cross-functional coordination, contract administration, vendor artifact management, FMV documentation, audit-ready repository maintenance, process improvement.
Preferred skills
Biopharmaceutical industry experience, HEOR operations, clinical operations, iEnvision Research Module, Veeva Vault, automation and AI-enabled tools.
Technologies
iEnvision Research Module, Veeva Vault, document repositories, procurement systems
Responsibilities
Receive and log evidence generation and contracting requests; conduct completeness checks and route requests; coordinate cross-functional review logistics; maintain study documentation checklists and status trackers; prepare study status summaries; apply close-out procedures and store final packages; support FMV documentation and contracting initiation; store vendor artifacts and contract records; identify process gaps and support improvements.
Seniority
Manager, hands-on IC
