Role: Senior Clinical Trial Manager II
Location: Remote
Duration: minimum 12+ months contract
Years of experience targeting: 3-5 years of experience in clinical research
- Customize/update any study-specific plans and process flows for multiple clinical vendors, as appropriate e.g., TMF Plan, site training plan, site monitoring plan, cross functional data review plan, IP release plan etc.
- Ensure quality of the trial master file through content (QC) review of document packages submitted for entry into the TMF and liaise with project teams to resolve any issues identified with the documents submitted.
- Assist CPL by tracking compliance to all study level plans and escalating any variances.
