Posted:
12/18/2025, 11:00:44 PM
Location(s):
Masovian Voivodeship, Poland ⋅ Prague, Capital City of Prague, Czechia ⋅ Budapest, Hungary ⋅ Capital City of Prague, Czechia
Experience Level(s):
Mid Level ⋅ Senior
Field(s):
Legal & Compliance
Responsible for coordinating the operational and strategic aspects for Clinical Trial Submissions
Essential Functions:
- 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
Qualifications
- 3 to 5 years experience building RDC databases in support of clinical research
- Experience in regulatory and submissions
- Project management skills
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
Website: https://iqvia.com/
Headquarter Location: Danbury, Connecticut, United States
Employee Count: 10001+
Year Founded: 1982
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Analytics ⋅ Health Care ⋅ Life Science