Empowering Clinical Operations Teams 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. 

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Why ClinOps Teams Prefer TransPerfect for Clinical Operations Management

Our knowledge and experience in ClinOps are evidenced by our ability to create and curate strategic clinical operations management 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.

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    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. 

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    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. Our experts also address the lack of diversity in clinical trials and increase patient engagement. 

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    Training and Development

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

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    Medical Writing

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

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    AI Data Solutions

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

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    Translation Services

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

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    Clinical Trial Disclosure

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

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    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

    Merck
    Gilead
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    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.

    Accelerating Pharma Labeling with Intelligent, Compliant Content

    White Paper

    Juggling multilingual labels across varying regions and products? Managing the updates and complying with local health authorities' requirements can be a challenge for global pharmaceutical companies, who are facing increasing pressure to streamline labelling processes and digitize labels. This white paper details how a unified eLabeling solution can eliminate duplication, improve accuracy, and deliver measurable ROI. ...

    Accelerating Pharma Labeling with Intelligent, Compliant Content
    Blog

    Health Canada's Transition to XML: What Regulatory Teams Need to Know

    In a continued push toward modernization and transparency, Health Canada has entered the next phase of its digital transformation with a mandate requiring the use of advanced extensible markup language product monograph (XML PM) files. This change builds on earlier...
    Webinar

    LifeSci Talks COA Series | Balancing Innovation and Integrity: AI’s Place in Patient-Focused Research

    Artificial intelligence is redefining what’s possible across the clinical development lifecycle, but with rapid innovation comes the need for thoughtful oversight. In this episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, sits down with ...
    White Paper

    Web Localization Playbook for Life Sciences

    The life sciences industry relies on websites to connect with patients, sites, and global audiences. Whether you're launching a patient recruitment campaign or managing an international healthcare marketing initiative, localization ensures your message is not just understood ...
    Webinar

    Rewriting the Rules of Informed Consent Development with AI

    Regardless of the market a clinical trial is being conducted in, getting locally approved informed consent forms (ICFs) consume as much as 12% of a clinical trial budget before it even begins. Each ICF must be clear and delicately balance local regulations and patient ...
    Guide

    Multilingual IMP Labeling Quick Guide

    Meet global regulatory expectations the first time with these efficient, cost-effective, and compliant product labeling solutions and considerations. ...
    Event

    OpTImize London

    - | Park Plaza London Westminster Bridge 200 Westminster Bridge Road London, England, United Kingdom, SE17UT ...

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