TransPerfect Life Sciences

AI and automation are changing how medical affairs teams work, helping them manage information, improve collaboration, and focus on higher-value activities. Our latest blog discusses how technology can support scientific exchange, streamline review cycles, and strengthen global communication. It also includes practical advice to help medical affairs teams adopt AI responsibly. Check it out here: https://lnkd.in/eej3XaTv #MedicalAffairs #LifeSciences #AI

Hello from Fierce Biotech Week 2025 in Boston! Come visit the TransPerfect Trial Interactive team at Booth 317 through Thursday afternoon to connect with our team — and learn how we’re helping sponsors and CROs accelerate global trials with confidence. Plus, don’t miss Laurel-Ann Schrader’s session tomorrow at 10:15 AM: “A Risk-Based Approach to Trial Management and the TMF”, to learn how to improve oversight, streamline processes, and keep the Trial Master File inspection-ready at every stage. #FierceBiotechWeek #ClinicalResearch #TMF

Our latest episode of LifeSci Talks is here! What does meaningful patient involvement really look like in health technology assessment? Mark Wade, Global Practice Leader at TransPerfect Life Sciences, is joined by Alice Biggane, Outcomes Innovation and Research Lead at Pfizer UK, to explore how HRQoL and PRO data influence reimbursement and cost-effectiveness—and what’s next for inclusive, patient-driven HTA. Listen here, or wherever you get your podcasts: https://lnkd.in/dWUZx2pU #HTA #PatientEngagement #ClinicalTrials

Join Katherine Cianciarelli and April Mattison-Wolfe from Trial Interactive at OCT NE for the panel: "Beyond Integration: How AI Creates a Clinical Trial Platform" They’ll explore how AI is solving the challenge of disconnected systems by: 🔵Enabling natural language queries across eTMF and CTMS 🔵 Driving inspection readiness through document quality 🔵 Connecting documents and operations for predictive trial health 🔵 Automating workflows with smart classification Heading to OCT NE? Contact us today to schedule a meeting—we’d love to connect. #OCTNE #ClinicalTrials #TrialInteractive

Registration is now open for Cohort 4 of TMF University! Whether you're new to the Trial Master File or ready to level up your TMF expertise, TMF University is the only TMF education program accredited to IAOCR - International Accrediting Organization for Clinical Research global standards. In this cohort, you’ll gain the knowledge, confidence, and practical skills to succeed in real-world TMF roles. From essential document strategy to inspection readiness and quality control, our curriculum is designed to help you think critically and work effectively. Cohort 4 begins in October! Secure your spot today and take the next step in your TMF career. Register here: https://lnkd.in/ghbkzNXq #TrialMasterFile #ClinicalResearch #NeverStopLearning

AI integration in clinical trial quality management isn’t here to replace the work of quality professionals. Instead, it introduces opportunities to help them do their jobs more efficiently, confidently, and proactively. In this article, Trial Interactive's VP of Product Management, Jay Smith, shares insight on how probabilistic systems enhance the three pillars of your QMS: LMS, QDMS, and quality events management. Read the blog ➡️ https://lnkd.in/eyM7mdMe #TrialInteractive #HITL #QualityManagement

In global clinical trials, accurate and culturally appropriate COA localization is critical to protecting both patient understanding and data integrity. Join us for our upcoming webinar featuring Alexandra Crane, Vice President of COA, Digital Health, and Regulatory Solutions at TransPerfect Life Sciences, for a live session that will explore: 🔵 The importance of language validation in COA 🔵 Regulatory expectations and QA for multilingual data 🔵 Practical insights from oncology and rare disease case studies Reserve your spot today: https://lnkd.in/ebETmJvZ #COA #eCOA #ClinicalTrials

We’re heading to Fierce Biotech Week, October 7–9 in Boston! This event brings together industry leaders to discuss the future of biotech, and we’re thrilled to share that Laurel-Ann Schrader will be a featured panelist. When: October 8, 10:15–11:00 AM ET Panel: Risk-Based Approach to Trial Management & the TMF Laurel-Ann will share practical insights on how teams can embrace risk-based strategies to improve oversight, streamline processes, and keep the Trial Master File inspection-ready at every stage. Join us in Boston for a week of learning, networking, collaboration, and be sure to catch this panel! #TrialMasterFile #ClinicalResearch #RiskBasedApproach

Discussion about AI is everywhere, but what does effective AI implementation look like at a life sciences organization? From compliance to data security, life sciences organizations face unique hurdles when it comes to adopting AI. In our latest blog, we explore how governance, adoption strategies, and purpose-built AI tools are reshaping the life sciences industry. We also explore real-world use cases show how AI is already creating measurable impact while ensuring trust with patients, providers, and regulators. Read it here: https://lnkd.in/ebf5C6ce #GenAI #LifeSciences #Pharma

AI is transforming the way life sciences teams manage pharmacovigilance, but how can you unlock these efficiencies without compromising patient safety? On October 23 at 11AM IST, join TransPerfect Life Sciences and our expert speakers for a live discussion on: 🔵 Practical use cases of AI in pharmacovigilance 🔵 Key considerations for ensuring compliance and patient safety 🔵 Lessons learned from leading organizations in the field Secure your spot today: https://lnkd.in/e9r8n2H9