Remote Clinical Research Specialist

REMOTE Clinical Research Specialist ( Medical Device)- 6 months contract- May go perm

Responsibilities

o Will work closely with Clinical Controls and Clinical Operations team members to ensure the timely QC approval or remediation of clinical trial essential documents based on GDP standards, the project eTMF Index, and company's SOPs.

o Review docs from the site an determine if the docs are complete, accurate and named appropriately and filed in the correct area (QA) if not correct and let the team know.

Qualification

5 + years, BA required. o Working as CRA (clinical research associate.)

o Familiar GDP (good documentation practices)

o Filling clinical trial documents ETMF

o Preferred, experience with electronic file system, Medidata and Sharepoint & Smartsheet.

Interview Process: Virtual panel.