Assoc Lab Project Set-up Mgr
On-siteBuenos Aires, Buenos Aires F.D., Argentina
Job Summary
Manage the design and launch of clinical research studies, owning start-up deliverables and ensuring quality execution across sponsors, CROs, and internal teams. Develop and manage study database design requirements for protocols, amendments, and sponsor changes while configuring databases in alignment with clinical protocols. Act as the primary set-up point of contact for stakeholders and coordinate activities across Data Management, Logistics, Clinical Trial Materials, and Specimen Management. Maintain project timelines, action logs, and status reports, proactively managing scope changes and risks. Requires a Bachelor's degree in science and experience with clinical study database design. Join IQVIA Laboratories in Buenos Aires to accelerate research and development.
Required Qualifications
- Bachelor's degree in science or a related field
- Experience with clinical study database design and configuration
- Working knowledge of Clinical Trials Management Systems
- Proficiency with Microsoft Office applications
- Strong understanding of clinical research terminology and ICH E6 Good Clinical Practice guidelines
- Excellent organizational, time management, and attention to detail skills
- Ability to work effectively in a fast-paced, deadline-driven environment
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