Digital Study Expert – Clinical Operations & eCOA

Our client, a leading global biopharmaceutical organization, is seeking a Digital Study Expert to support the implementation of digital solutions in clinical studies. The role focuses on managing the end-to-end lifecycle of digital health tools while coordinating between international study teams and technical vendors.

• Support the implementation and lifecycle management of eCOA digital solutions in global clinical studies.
• Coordinate requirement gathering, translations, and vendor quotes to ensure project alignment.
• Participate in digital solution workshops to document requirements and track technical configurations.
• Update training materials and documentation following periodic software releases.
• Facilitate stakeholder meetings and support clinical site trainings to ensure successful digital tool adoption.
• Develop basic analytics dashboards and patient evidence reports for study monitoring.

• 1+ years of experience within clinical operations environments such as CTA, CTO, or CRA.
• You bring practical knowledge or a strong interest in eCOA, ePRO, and patient-centric digital platforms.
• You possess experience in coordinating requirements and vendor documentation for digital solutions.
• You're highly organized with the ability to manage multiple ongoing clinical studies simultaneously.
• You have a proactive and adaptable mindset with the ability to navigate complex stakeholder environments.
• You are fluent in English.

Nice to Haves

• Previous experience with Veeva platforms.
• Knowledge of eCOA or ePRO vendor landscapes.
• Willingness to grow into a lead role within digital clinical operations.
• Basic knowledge of French or Dutch.

• Start date: ASAP
• Duration: until December 2026 with possibility of extension
• Work regime: Full-time
• Location: Brussels
• Working model: Remote
• Contract: open to both permanent employees and freelancers