--- title: "Clinical Expert Services & Flexible Resourcing for Clinical Trials | QbD Group" description: "Add CRAs, CTAs and clinical project managers to your clinical team across Europe. Flexible resourcing and FSP support without outsourcing your full study." url: https://qbdgroup.com/en/services/clinical-solutions/clinical-expert-services type: "Page" language: en publisher: "QbD Group" citation: "QbD Group, \"Clinical Expert Services & Flexible Resourcing for Clinical Trials | QbD Group\", https://qbdgroup.com/en/services/clinical-solutions/clinical-expert-services" --- # Clinical Expert Services and Flexible Resourcing Functional service provision and flexible resourcing for clinical operations Add clinical research professionals to your team, in the countries where you need them. You manage the study. We fill the gap. We work with medical device, IVD, pharma, biotech and hospital sponsors. ## What are clinical expert services and flexible resourcing? We supply **clinical research professionals** for short-term and long-term needs, across every therapeutic area and every industry we serve. Our people work inside your team, under your SOPs. We support start-ups, growing biotech, established pharma, medical device companies and hospitals. ## When teams use flexible resourcing ### You lack coverage in a country Your project managers sit in-house. Your trial runs across Europe. You have no monitor in Poland, Spain or France. ### Someone leaves, the study continues Maternity leave. Long-term illness. A resignation mid-study. Permanent recruitment takes months. Your trial does not pause. ### Your trial grows faster than your headcount Site numbers rise. Headcount approval lags. Add capacity without a permanent hire. ## 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. ## Three ways to work with us From one professional to a full study. Start anywhere on the scale. | | Flexible resourcing | Functional service provision (FSP) | Full study outsourcing | What you contract | One professional, or a few | A function, or part of one, such as monitoring in selected countries | The complete study | Who manages delivery | Your team | QbD, against agreed scope | QbD | How it works day to day | Our professionals work inside your team, under your processes and systems | We cover the scope you do not, alongside your own people | We run the trial and report to you | Typical commitment | Short, extendable | Longer term, scope-based | Project duration | Start here when | You have specific gaps to fill | You cover some countries or functions, not all | You have no in-house clinical team Sponsor responsibility stays with you in all three models. Most clients start with one person. Some grow into a wider programme. If you need a partner to run the whole trial, see our [clinical CRO services](https://qbdgroup.com/en/services/clinical-solutions). ## How can we help? Our clinical expert services cover a variety of clinical roles, **customised to your exact need in terms of expertise, duration and FTE**. #### Clinical Research Associate (CRA) Site selection, initiation, monitoring and close-out. On-site and remote. #### Clinical Trial Assistant (CTA) Trial master file, site documentation, study administration. #### Clinical Project Manager (CPM / CSM / CTM) Study planning, vendor oversight, timelines and budget. #### Also available through our network - Study Coordinator / Study Nurse - Medical Writer - Clinical Regulatory Specialist - Clinical Auditor - Clinical Safety Associate - Medical Monitor / Advisor Need a role outside this list? **Ask us.** Our network across the globe reaches further. ## 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 Why QbD Group ## Your trusted partner Within the clinical division of QbD Group, we combine clinical research expertise across medical device, IVD, pharma and biotech with flexible resourcing tailored to your needs. Our network covers Europe and beyond, with expertise across therapeutic areas including cardiovascular, neurovascular, orthopedics and ophthalmology. We develop our people through an internal training programme and work to ICH-GCP, ISO 14155, MDR, IVDR and EU-CTR. Flexible support, from one professional upward Experienced clinical research professionals Own teams in Belgium, France, the Netherlands, Spain, Germany and Poland, monitoring across Europe ICH-GCP, ISO 14155, MDR, IVDR and EU-CTR expertise FAQ ## Frequently Asked Questions ### ### ### ### ## Tell us which role you need Send us the role, the country and the start date. We come back with profiles. Request a profile --- Source: https://qbdgroup.com/en/services/clinical-solutions/clinical-expert-services — © QbD Group. Quote freely with attribution and a link back.