Cristina Guerra Laurie is the Country Manager at TransPerfect Spain, where she leads a dynamic team of consultants focused on delivering tailored eClinical and eTMF solutions through the Trial Interactive platform. With over 20 years of experience in localization, training, and contract research, and 15 years specializing in the Life Sciences industry, Cristina helps global clients accelerate clinical trials, ensure regulatory compliance, and reduce costs and risks.

Gillian Gittens is a TMF industry veteran with over 25 years’ experience, has a wealth of insight and expertise in managing TMF services and delivering ongoing customer success across all aspects of TMF operations. A key member of the CDISC TMF Reference Model Steering Committee and Project Management Team leading the V4 initiative, Gill has key expertise and insight in industry best practice, regulatory guidance and the future of TMF management.

Avani Amin has 18 years’ experience in TMF Management and oversight, having worked across multiple FSP TMF providers. Initially key member of the Project Management team supporting clients across the top 30 global pharmaceutical firms, Avani now co-leads the eClinical Solutions Management unit and the Study Owner unit at Trial Interactive, directing TMF Oversight across 200 keystone clients. In this capacity, she regularly oversees system implementation, provides best practice guidance, and ensures ongoing customer success for Trial Interactive premier clients. Avani leverages her 18 years in the industry to provide accurate, clear TMF consulting for a range of customers; assisting clients with industry best practices, optimization of eTMF and CTMS systems, business process development, and SOP/TMF plan creation. As the industry evolves with the onset of new technology, she is well placed to communicate accurately Regulatory expectations and TMF requirements to ensure clinical compliance across the CDGM space.

Carlos has been supporting Sponsors & CRO in the TMF FSP space for 10 years; and has supported 50+ eTMF implementations and 30 FSP model activations in the last 18 months. Working across multiple support models, he remains a market leading expert in adaptable compliant workflows for full TMF compliance. He works directly with sponsors, providing full TMF management, alongside CROs as a collaborative partner, and advises on appropriate technology platforms and configurations based on client need. He also sits at the forefront of the TransPerfect AI rollout, helping with AI for TMF Management and Medical writing.

With 19 years in clinical research, Eva Matheu brings deep, hands-on experience from CTA to auditor across Sponsors and CROs in Europe and Latin America. For over a decade, she has specialized in TMF audits and now works as a Senior TMF Consultant—helping organisations stay inspection-ready. From gap analyses to tailored workshops and strategic TMF guidance, her work ensures quality and compliance at every step. She’s also an active CDISC volunteer, contributing to key industry initiatives shaping the future of clinical trial documentation.