Lotus Clinical Research is seeking a TMF Specialist to support Regulatory Operations by managing, reviewing, and approving site-level documentation within the eTMF. You will ensure timely filing, audit readiness, and compliance across study activities, collaborating with internal teams and vendors to uphold documentation standards and regulatory expectations.
The ideal candidate has 1 year of clinical research or regulatory documentation experience and familiarity with Veeva Vault or similar
#J-18808-LjbffrRemote TMF Specialist: Regulatory Operations in Remote at Unknown Company
This position is listed as full time and onsite.