Empowering ClinOps with Global Content Solutions

Clinical operations professionals need the resources to efficiently handle clinical research. Throughout clinical trials, TransPerfect provides seamlessly connected solutions and services to support your success. 

Get in Touch
Clinician using clipboard to mark off drug information

Why ClinOps Teams Love TransPerfect

Our knowledge and experience in ClinOps are evidenced by our ability to create and curate strategic solutions to improve their day-to-day operations and reduce administrative burdens. 30+ years of making these solutions for you specifically. Here are some of your options:

    eClinical Solutions

    Scale and grow with eclinical solutions for every stage of the clinical trial lifecycle, our seamlessly connected platform streamlines and automates essential clinical processes across thousands of studies for sponsors, CROs, and sites around the world.

    Learn More

    COA/eCOA Solutions

    Access end-to-end consultation, from licensing to electronic clinical outcome assessment (eCOA) migration, and improve the patient and healthcare provider experience with all types of COAs.

    Learn More

    Patient Engagement

    With extensive market research and global expertise, our local digital marketing experts develop strategic recruitment marketing plans and messaging that engage patients across all channels.

    Learn More

    Training and Development

    Technical and instructional design expertise to create and deploy engaging training content that keeps your global life sciences team compliant.

    Learn More

    Medical Writing

    Ensure speed, quality, and compliance for all of your scientific communication, regulatory documentation, disclosure, and medical education.

    Learn More

    AI Data Solutions

    Scalable and secure data collection, annotation, and chatbot translation services.

    Learn More

    Translation Services

    Navigate global clinical, corporate, and commercial operations under stringent regulatory compliance requirements while providing fast, accurate multilingual communications.

    Learn More

    Clinical Trial Disclosure

    Our experience, expertise, and technology support product launches across global markets and expand your clinical research worldwide while maintaining regulatory compliance.

    Learn More

    A Faster Way to Launch and Manage Your Global Clinical Operations

    ClinOps, from planning to implementation, is complex. Do you have the support and tools you need to simplify your clinical trial processes? TransPerfect has a suite of solutions to help you reduce costs, relieve administrative burdens, and shorten the path to breakthroughs.

    Trusted by Life Sciences Organizations Big and Small

    News and Thought Leadership

    Industry insights from our experts. We have the experience and solutions you need to navigate life sciences complexity and bring breakthroughs from lab to launch.

    The C3 Summit: Boston Recap

    The second event in our series of C3 Summits took place in Boston on May 16, 2023. We invited industry experts and leaders to discuss challenges, opportunities, and strategies in clinical trial diversity, centricity, and outcome assessments through the lens of real-world experience. In this recap of the Boston session, we will review key points from each session.  Session 1: COA/eCOA Innovations – Licensing Hiccups, Linguistic Validation, ePRO Migration, and Best ...

    The C3 Summit: Boston Recap

    How Medical Writing Can Drive Patient Engagement

    Medical writing is a critical component of the broader patient engagement landscape, establishing the foundations of communication between pharmaceutical companies and patients. The quality of medical communication can be transformational in how a patient engages with and...

    A Conversation with Dr. Elin Haf Davies of Aparito

    The rare disease space presents numerous challenges for clinical research and patient data capture. These challenges are only heightened for younger patient populations, where outcome measures and dosages need to be considered appropriately. Join Dr. Elin Haf Davies, Founder & ...

    Navigating the EU Clinical Trial Regulation Complexities - Current Challenges and Opportunities

    As the most significant change in the European Union clinical trial legislative ecosystem in 20 years, the European Union Clinical Trial Regulation 536/2014 (EU CTR) went live on January 31, 2022. The first-year transition period has now ended, and from January 31, 2023, EU ...

    How to Maximise Value and Avoid Failure During Life Sciences Dealmaking

    Please complete the form below to access the on-demand recording of our webinar. A fantastic expert panel of life sciences dealmaking veterans from AstraZeneca and Merck, with 100 years' collective experience, share their insights on key dealmaking strategies, best practices ...

    Centralizing Global Content Solutions for Medical Affairs

    With a rapidly evolving landscape and the introduction of new technologies and emerging therapeutics, medical affairs professionals are tasked with remaining in lockstep with the latest industry developments. From a content perspective, this means not only maintaining clear...

    Automation for MDR & IVDR: A Three-Part Seminar - Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements

    Part 3: EnCompass Step by Step: A Detailed View of the Content Automation Solution to Meet MDR & IVDR Requirements ...

    Need Support with Your Clinical Operations?

    Schedule a free consultation. 

    How did you hear about us?
    This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.