Lotus Clinical Research offers a fully remote TMF Specialist role focused on managing and approving site-level documentation in the eTMF. You will ensure timely filing, audit readiness, and compliance across study teams.
Ideal candidates have a biology-related degree and at least 1 year in clinical research or regulatory operations, with strong attention to detail and proficiency in Microsoft Office. Veeva Vault experience is preferred.
#J-18808-LjbffrRemote TMF Specialist, Regulatory Operations in Remote at Unknown Company
This position is listed as full time and able to be worked remotely.