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.

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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.

    Potential Impact of the EU Biotech Act Proposal on Clinical Trial Activities

    The European Commission’s proposed Biotech Act introduces changes that could reshape how clinical trials are approved and managed across the EU. While the broader package spans multiple areas of the health ecosystem, proposed updates to the EU Clinical Trial Regulation (EU CTR) stand out for their potential to address long-standing operational challenges including lengthy timelines, limited flexibility in submissions, and fragmented processes across member states. ...

    Potential Impact of the EU Biotech Act Proposal on Clinical Trial Activities

    A Checklist for eCOA Solution Deployment: Best Practices and Considerations

    Selecting and deploying a new eCOA solution involves many important factors - from determining the capabilities of the Language Service Provider (LSP) to identifying the technology used for each COA migration - and it’s impossible not to worry about missing a key detail in the ...

    Fortune 500 Pharma Company Meets Critical Deadlines with TransPerfect Life Sciences’ COA Solutions

    This spotlight reviews the challenges faced by a Fortune 500 pharmaceutical company in implementing Clinical Outcome Assessments (COAs) to measure the impact of their products on patients. It discusses the need for accurate and culturally appropriate translations of COAs for ...

    Successful English Build & Language Migration

    Over the past decade, the global clinical trial landscape has changed drastically. A surge in technological innovation, including wearable devices, patient portals, and apps, has modernized how clinical data is collected and managed. With pen and paper becoming obsolete in the ...

    Why 75% of Medical Device Manufacturers Are Disappointed with Their AI Results

    The Gap "The results we're seeing from AI are only as good as the data and structure we put behind it. Most manufacturers haven't done that work yet." — Marc Miller, Division President, TransPerfect Medical DeviceArtificial intelligence has arrived in medical device...

    Metadata In, Metadata Out: Reducing RIM Submission Rework with In-System Translation

    Pharmaceutical companies spend billions and take years to bring therapies to market. Then many risk it all on a translation process managed with spreadsheets, email chains, and blind faith. Every label update, every safety amendment, every regulatory change notice must be...

    AI Content Creation and Maintenance in Medical Information: Ending the Content Whack-a-Mole

    For many medical information (MI) teams, content maintenance can often feel like a game of whack-a-mole.Update one answer, three more pop up. Fix a regional version, and another channel drifts out of sync. Add a new piece of literature, and suddenly every approved response...