Our CRO Services

Supporting your clinical development needs

Simbec-Orion is a full service CRO, providing clinical management services from phase 1 to phase 3, plus additional clinical support. We have the capability to run fully integrated clinical trials, or provide stand-alone support for many aspects of your trials.

We aren’t the largest full service CRO, which comes with benefits: your trials will gain from the broad experience of a large organisation, with the compassion, personal service and care of a small one.

Discover our range of CRO services below, or get in touch to submit an RFI or RFP.

Central Laboratory

We are a CRO with in-depth experience in the most challenging therapeutic areas, including oncology, rare and orphan diseases, respiratory, dermatology, vaccines and anti-infectives.

With more than 25 years’ experience in the clinical research sector, we offer a comprehensive service you can trust – with an international reach. All with the highest level of quality, agility, and responsive customer service.

Clinical Trial
Management Services

Our expert biometrics team delivers accurate and adaptive clinical data management services that support the success of your drug development programme.

Conducting statistical analysis, planning, and reporting across all clinical phases, they will create a quality biostatistical framework that presents clinical trial data clearly and correctly for regulatory agencies.


As a full-service facility, we carry out all types of studies at our purpose-built site. 90% of our work is with Investigational Medicinal Products, in all drug delivery routes.

Clinical pharmacology is a key part of our CRO services, so if you need support managing a clinical trial, there are many ways our expertise can help.


Responding to the evolving needs of our clients has made us the contract research organisation we are today. Offering a full-service clinical development portfolio, but with the size, agility, and structure to respond rapidly when needed. With a team of experienced management, clinical research and scientific advisory specialists, we deliver precise clinical development solutions with expertise.


Gamma scintigraphy can play a vital role in drug product development, facilitating the determination of the biodistribution of dosage forms under physiological conditions. As such, it’s a core part of our CRO services.

Featuring an on-site scintigraphy suite and a long-standing partnership with Cardiff Scintigraphics Limited, Simbec-Orion has been providing integrated scintigraphy services for more than 25 years.


Our pharmacovigilance specialists will help you assess the potential risks of your drug product, with a core focus on drug safety.

Through the collection and continuous evaluation of clinical safety data throughout the clinical development process, they will assess and monitor the incidence of adverse drug reactions (ADRs).

We have over 40 years experience in first-in-human and early phase studies. Learn what it’s all about at Simbec-Orion.

What our
Clients Say About Us

The people working at Simbec Orion are dedicated, very professional and they cover all aspects of clinical research. A team will be set up for your project, who will have a strong focus on your study in a very open minded and friendly atmosphere. The studies I have outsourced to Simbec Orion, have been successfully managed and performed. I will use Simbec Orion in the future and I can strongly recommend them to other pharmaceutical companies.

Tina Lidén Mascher, Head of Clinical Operations

Klaria AB

Got a question?
Get in Touch or Submit an RFI/RFP

Our team is on hand to answer any questions you might have relating to the work we do at Simbec-Orion. Just fill in the form below, making sure to tick the boxes that apply, and we’ll respond as quickly as we can.

Looking to volunteer for a clinical trial?

Visit our dedicated volunteer website here, or email enrolmentservices@simbecorion.com

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