Senior CEVA Specialist

South Africa / Slovakia

Homebased

Join us in driving excellence across global clinical research programs. Are you a proactive leader with deep clinical research expertise and a passion for delivering high‑quality outcomes for customers? We’re looking for a Sr CEVA Specialist to provide strategic oversight and operational excellence across Endpoint Adjudication Management (EAM) and Oversight Group Management (OGM) projects. This is your opportunity to work cross‑functionally on complex, high‑impact programs that help shape the future of healthcare.

🔍 About the Role

As a Sr CEVA Specialist, you will manage and deliver comprehensive Clinical Event Validation and Adjudication (CEVA) services, supporting committees such as:

Endpoint Adjudication Committees

Core Laboratories

Image Review Committees

Data Monitoring Committees

Safety Monitoring Committees

Steering Committees / Advisory Boards

You’ll serve as a trusted customer partner—guiding projects from scoping and proposals through delivery, ensuring clarity, transparency, and exceptional service every step of the way.

⭐ What You’ll Do

Lead and coordinate adjudication and oversight committees across CEVA service lines

Serve as the primary customer interface, ensuring strong communication and timely deliverables

Develop project-specific documentation, reports, listings, and training

Collaborate with internal/external teams to develop and optimize electronic systems

Manage project profitability, revenue forecasting, and financial performance

Mentor developing specialists within the CEVA team

Identify risks and implement innovative process improvements using Lean methodologies

Support proposal development, bid defenses, and sales presentations

Participate in audits, inspections, and high-level customer meetings

Manage multiple, complex projects with competing priorities

Drive customer loyalty through exceptional service delivery

🎓 Qualifications & Experience

Bachelor’s degree in Life Sciences, Health Sciences, or equivalent

5+ years of clinical research experience

Prior customer-facing experience is essential

Solid knowledge of GCP, ICH guidelines, and relevant regulatory standards

Strong project management capability and ability to lead teleconferences and meetings

Excellent communication, organizational, prioritization, and problem‑solving skills

Ability to manage ambiguity and work independently across multiple projects

Skilled in conflict resolution, influencing others, and strategic thinking

Cross‑trained in at least two CEVA service lines (preferred)

Financial awareness, including budgeting and revenue management (or willingness to develop)

🌐 Why Join Us?

Work fully remote

Shape best‑in‑class CEVA practices and customer experiences

Collaborate with global clinical experts

Drive meaningful change in healthcare research

Work on diverse, complex, and rewarding projects

Grow your leadership, technical, and strategic capabilities

👉 Ready to make an impact? Join us and help deliver excellence across global clinical event adjudication. Apply today!

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.