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-Powered Literature Monitoring for Medical Affairs & Medical Information Teams

    Written by: Gigi Shafai, Pharm.D., Vice President, Medical Affairs & Digital Transformation, TransPerfect Life Sciences Streamline your global literature monitoring activities and facilitate your Medical Affairs workflows and content development with AI-Powered literature monitoring Medical Affairs and Medical Information teams are tasked with staying informed on the latest clinical research, regulatory updates, and scientific developments to make data-driven ...

    AI-Powered Literature Monitoring for Medical Affairs & Medical Information Teams

    Fast, Compliant, Centralized Translation in Action: Lessons from AbbVie & Immunovant

    Due to high interest following our GlobalLink NEXT panel, we’re welcoming back Stacey Higgins, Associate Director, COA & Digital Implementation Team of AbbVie alongside Tihirah Harris, Sr Manager, Clinical Business Operations of Immunovant to share how and why they moved to a ...

    Improving Learning Outcomes in Life Sciences Through Data-Driven Benchmarking

    In life sciences, strong training programs are essential, but knowing whether they’re actually effective can be a difficult endeavor. In this session, Amanda Hernandez, Director of Sales Training & Effectiveness and Barrett Gaylord, Sales Training Lead of Telix ...

    How Patients Discover Clinical Trial Websites: The Role of Localization in Search and Trust

    Could localization be the key to improving patient recruitment in clinical trials?Recruiting participants for clinical trials is a critical step in bringing new therapies and treatments to market, but despite advances in digital outreach, the industry still faces major...

    LifeSci Talks COA Series | Modernizing eCOA: Emulators, Backups, and the Future of Reporting

    In this tech-forward episode of LifeSci Talks, Mark Wade, Global Practice Leader at TransPerfect Life Sciences, welcomes Indira Jain-Figueroa, Product Director at Evinova, for a deep dive into the ever-evolving landscape of eCOA development. Covering everything from cross ...

    Rewriting the Rules of Informed Consent Development with AI

    How AI and Structured Content Management Are Transforming the ICF ProcessInformed consent forms (ICFs) are essential to clinical trials, serving as the primary vehicle for communicating study information to participants in a clear, ethical, and compliant manner. Given...

    Could Data Standardizations be the Silver Bullet for Faster Electronic Clinical Outcome Assessment (eCOA) Deployment?

    Choosing an electronic clinical outcome assessment (eCOA) provider is a complex process that involves a variety of different aspects including experience, scientific support and knowledge, integration capabilities, scalability, study-specific requirements, and so much more. ...

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