related to the electronic Trial Master File (eTMF) and ensure compliance with internal policies as well as external... and company culture, visit us at | Who You Are Reporting to the Senior Manager, TMF Operations, the TMF Specialist...
essential documents in the Trial Master File (TMF) What we are looking for in a Clinical Trial Specialist: BS or higher...R&D Partners is seeking to hire a Clinical Trial Specialist in the San Francisco Bay Area. Your main responsibilities...
representative and take meeting minutes as requested. Oversee and manage essential documents in the Trial Master File (TMF...Study Specialist II W2 Contract Salary Range: $83,200 - $93,600 per year Location: Novato, CA - Hybrid or Remote...
(s) as GSO representative and take meeting minutes as requested. ● Oversee and manage essential documents in the Trial Master... File (TMF) ● Contribute to Global Study Operations risks identification and mitigations. ● Provide support...
. ● Oversee and manage essential documents in the Trial Master File (TMF) ● Contribute to Global Study Operations risks...Title: Study Specialist II Location: San Rafael, CA (Hybrid 2 Days/week) Duration: 10+ Months Role Summary...
as a representative and take meeting minutes as requested. Oversee and manage essential documents in the Trial Master File (TMF...Role Summary The Study Specialist II contributes to or leads tasks related to the oversight of site monitoring, site...
will ensure each Trial Master File can fully reconstruct the conduct of a clinical trial and those documents are readily... device industry with at least 3 years' experience in Clinical Trial Master File management is required. EDUCATION...
Ensure each Trial Master File can fully reconstruct the conduct of a clinical trial and those documents are readily... in Clinical Trial Master File management is required. Expertise with Good Clinical Practices (GCPs), International Conference...
Document Manager remotely in the United States. The Clinical Document Manager role will ensure each Trial Master File can fully... pharmaceutical, biotechnology or medical device industry with at least 3 years' experience in Clinical Trial Master File management...
the benefits of drugs for patients. Duties: TMF Management Ensure each Trial Master File can fully reconstruct the... conduct of a clinical trial and those documents are readily available for audits/inspections. Ensure defined TMF file...