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Digital Study Expert

Key Facts

Remote From: 
Fixed term
English

Other Skills

  • Training And Development
  • Accountability
  • Communication
  • Adaptability
  • Multitasking
  • Time Management
  • Teamwork
  • Proactivity
  • Detail Oriented
  • Problem Solving

Roles & Responsibilities

  • Strong communication skills
  • Fluent English
  • High motivation to learn digital clinical operations
  • Ability to collaborate with multiple stakeholders

Requirements:

  • Supporting the Digital Study Lead across 3–4 ongoing studies
  • Gathering and tracking eCOA requirements, translations, and vendor quotes
  • Participating in myVeeva workshops, taking notes, documenting requirements
  • Updating training materials after myVeeva releases (3×/year)

Job description

This is a remote position.

As a Digital Study Expert, you will play a pivotal role in supporting the operational implementation of digital solutions across our global clinical trial portfolio (Phases I–IV, including Non-Interventional Studies) in therapeutic areas such as Rare Diseases, Immunology, and Neurology. This role is integral to the successful deployment and execution of the myVeeva digital eCOA solution which aligns with UCB’s Patient Evidence ‘Ruby’ strategy and our strategic partnership with Veeva.

You will work closely with the Digital Study Lead, study teams, vendors, CROs, sites, and patients to ensure high-quality, compliance, and efficient digital study operations. This is a growth-oriented role with opportunities to develop into a future Digital Study Lead.

Typical Day
• Supporting the Digital Study Lead across 3–4 ongoing studies.
• Gathering and tracking eCOA requirements, translations, and vendor quotes.
• Participating in myVeeva workshops, taking notes, documenting requirements.
• Updating training materials after myVeeva releases (3×/year).
• Attending status meetings with CPMs and study teams.
• Supporting site and study team trainings (SIV, IM, virtual sessions).
• Hosting or supporting monthly Office Hours and maintaining an FAQ log.
• Creating simple dashboards or patient data reports (occasional).
• Ad hoc tasks: meeting minutes, slide creation, follow ups with stakeholders.


Requirements

Years of Experience
• 0–2 years acceptable
• Some exposure to clinical operations is strongly preferred (CTA/CTO/CRA environment).
________________________________________
Must Have
• Strong communication skills.
• Fluent English.
• High motivation to learn digital clinical operations.
• Ability to collaborate with multiple stakeholders.
• Strong organization and problem solving skills.
• Interest in clinical studies and patient centric digital solutions.
________________________________________
 Ideal Candidate
• Entry level profile (no Master’s; Bachelor’s is enough, not mandatory).
• Experience as a Clinical Trial Assistant or similar.
• Curious, proactive, adaptable, able to deal with ambiguity.
• Comfortable taking ownership and supporting multiple tasks simultaneously.
• Eager to grow into a Digital Study Lead role.
________________________________________
Nice to Have
• Additional European language (FR or NL helpful if based in BE).
• Basic knowledge of eCOA/ePRO vendors or digital platforms.
• Previous exposure to Veeva tools.
• Experience interacting with clinical project teams.


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