Regulatory and Start-up Manager
IQVIA
full-time
Posted on:
Location Type: Office
Location: Warsaw • 🇵🇱 Poland
Visit company websiteJob Level
Mid-LevelSenior
About the role
- Lead the submission process from strategy formation to clinical trial approval
- Coordinate creation of trial submissions strategy development, planning and delivery
- Responsible for Quality checks on CTIS before submissions
- Financial planning an tracking
- Driving discussions, consolidates inputs from stakeholders and facilitate CTR submission strategy
- Responsible for Coordinating submissions in the CTIS portal
Requirements
- 3 to 5 years experience building RDC databases in support of clinical research
- Experience in regulatory and submissions
- Project management skills
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
RDC databasesclinical researchregulatory submissionsfinancial planningquality checkssubmission strategy developmentproject management
Soft skills
leadershipcoordinationcommunicationstakeholder engagementfacilitation