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

    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.

    AI and MT "Ask and Expert" Office Hours - 4/10/2024

    TransPerfect's experts gather to answer questions from global pharma, biotech, and medical device leaders regarding AI and MT use cases, challenges, opportunities, best practices, and more. ...

    AI and MT "Ask and Expert" Office Hours - 4/10/2024

    Multilingual Labeling: Considerations for Efficient, Cost Effective and Compliance Labeling

    Accurate and compliant labeling of an investigational medicinal product (IMP) is an important and integral part of clinical trial operations. A misstep in labeling can lead to significant delays, affecting the entire study’s timeline and potentially incurring costs ranging from ...

    An Overview of Generative AI and Machine Translation for Life Sciences

    Global life sciences companies are realizing the potential artificial intelligence (AI) and machine learning (ML) has to drive efficiency in content and translation management. To capitalize on this, organizations need to identify the right solutions. Discover important ...

    6 Pathways to Take Your MT Strategy to the Next Level in 2024

    With 2024 well underway, innovators in the global life sciences and pharmaceutical industries continue to question how to maximize efficiencies and reduce complexities in clinical and regulatory content development and localization. As part of the broader technological roadmap, ...

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