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    Clinical Expert Services – Flexible, tailored staffing solutions

    Clinical Expert Services

    Flexible, tailored staffing solutions

    We provide life sciences companies with the skilled resources needed to execute clinical studies efficiently and compliantly. From clinical trial associates to medical writers and beyond.

    What are clinical expert services?

    We provide life sciences companies with the skilled resources needed to execute clinical studies efficiently and compliantly.

    From clinical trial associates to medical writers, our professionals bring expertise and adaptability for short-term or long-term needs. We support start-ups, growing biotech, established pharma, and hospitals.

    Clinical Expert Services

    Why is this important?

    Managing clinical studies requires the right expertise at the right time. Clinical expert services provides a flexible solution to fill resource gaps.

    Quick response

    Address resourcing needs as they arise, avoiding project delays.

    Cost-effective

    No long-term commitments or unnecessary recruitment costs.

    Global expertise

    Access to skilled clinical research professionals wherever your study takes place.

    Our process

    No two clinical studies are the same, so we take the time to understand your exact needs.

    1. Understand & match

    Brief intake conversation to understand unique needs and match with the right professional.

    2. Review & discuss

    Sharing tailored profiles and facilitating conversations with potential candidates.

    3. Finalize & execute

    Initiating the contract process quickly once a candidate is selected.

    Expert Services Process

    How can we help?

    Our clinical expert services can cover a variety of clinical roles and be customized depending on the exact need in terms of expertise, duration and FTE.
    Clinical roles we provide:
    • Clinical Trial Associate (CTA)
    • Clinical Research Associate (CRA)
    • Clinical Project/Study/Trial Manager (CPM/CSM/CTM)
    • Study Coordinator/Study Nurse
    • Medical Writer
    • Clinical Regulatory Specialist
    • Clinical Auditor
    • Clinical Safety Associate
    • Medical Monitor/Advisor
    Because of our extensive network across the globe, we can also assist you with other types of clinical research-related roles.

    What our clients say

    "For several years, we have been working with QbD Group, using their clinical expert services. We appreciate the short communication lines, the seamless fit of contracted profiles with our team, the high quality of their work, and their quick support in resolving any concerns. We have also recommended QbD Group to our American colleagues and they too have entered into a partnership."
    — Penumbra
    Penumbra is a global healthcare company focused on innovating novel technologies to help as many people as possible
    QbD Group expertise

    Why QbD Group

    Your trusted partner

    Within the clinical division of QbD Group, we combine extensive clinical research expertise across Medical Device, Biotech, and Pharma sectors with flexible resourcing options tailored to your needs. Our global network covers Europe and beyond, with diverse expertise in therapeutic areas including Cardiovascular, Neurovascular, Orthopedics, and Ophthalmology. We prioritize continuous development of our employees through an internal training program and maintain the highest standards of quality and regulatory compliance (ICH-GCP and ISO 14155).

    Flexible support.

    Experienced Clinical Research Professionals.

    Global coverage.

    Part of global CRO specialized in Medical Devices.

    FAQ

    Frequently Asked Questions

    Plan your clinical pathway

    From gap assessment to full CRO delivery, our clinical experts are ready to support your MedTech journey.