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
| 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.
How can we help?
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
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
为什么选择QbD Group
您值得信赖的合作伙伴
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
