Location: Fully Remote (Europe – Belgium preferred)
Engagement: Full-time
Contract: ASAP start – until Dec 2026 (possible extension)
Key Responsibilities
- Support Digital Study Leads across 3–4 global clinical studies using myVeeva eCOA.
- Track eCOA requirements, translations, and vendor quotes.
- Attend myVeeva workshops and document study/system requirements.
- Update training materials following system releases (3×/year).
- Join study status meetings and support site/team trainings (SIV, IM, virtual).
- Host/support monthly Office Hours and maintain an FAQ log.
- Create simple dashboards and patient data reports.
- General coordination tasks: meeting minutes, slides, follow-ups.
Requirements
Hard Skills
- 0–2 years’ experience; exposure to clinical operations (CTA/CRA/CTO) preferred.
- Understanding of clinical trial processes.
- Familiarity with digital platforms; Veeva experience is a plus.
- Ability to create simple dashboards/reports (Excel/BI tools).
- Strong documentation, tracking and organizational skills.
- Fluent in English (additional FR/NL is a plus).
- Comfortable working fully remote and collaborating across time zones.
Soft Skills
- Strong communicator, confident engaging with multiple stakeholders.
- Highly motivated to learn digital clinical operations.
- Curious, proactive, and adaptable; comfortable with ambiguity.
- Strong problem-solving skills and attention to detail.
- Able to multitask, manage parallel workstreams, and take ownership.
- Eager to grow into a Digital Study Lead role.
Job Type: Contract
Job Location: Belgium
Salary: Competitive