Your missing piece

Stiris Research Inc. is an entrepreneurial Clinical Trial Management CRO, providing comprehensive study management solutions for Phase I through Phase IIIB clinical research. We provide tailor-made services from full-service outsourcing to focused clinical study management.

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Built by biotech, for biotech

Your clinical development partner should bring more to the relationship than meets the eye. Stiris was formed as a result of listening to stakeholders engaged in clinical trials, identifying their unmet needs and developing a unique, value-base approach to address those needs.

Our cause has always been to help get life changing medications to patients. Our focus has always been on how to best take care of the patients who give of themselves and enroll in our trials. We look at how we can best serve the biotech and pharmaceutical community to be more efficient and move trials forward more quickly.

We critically review the protocol and collaborate with key stakeholders to proactively determine how to make study participation easier for patients and their caregivers. And we don’t stop there. Throughout the study we’re soliciting feedback for ways to improve on how we’re supporting those patients and caregivers. Enrolling patients into a study isn’t just about getting results for that study. It’s about taking such good care of your patients that they’ll want to participate in future studies, and they’ll advocate for you with others to promote their participation in clinical trials. When they do enroll, these patients will be just as passionate about making others better that they’ll stay and adhere to the requirements of the study through to their last visit.

This is in our DNA. It’s how we think and how we look at your protocol and your study. If you want to know how to: set your study up for success, get sites to engage, patients to enroll, and be the study everyone wants to go the extra mile to see succeed – talk with us, we’ll show you the way.

Part of the reason why so many sites have stopped participating in clinical research is our industry’s fault. For instance, companies want to get research completed with the lowest budgets possible, but then we inevitably see delays when it comes time to pay sites. We teach the sites how to execute the protocol, and we miss ensuring they can effectively and efficiently conduct the trial in a manner such that it makes good sense for their patients and for their business. We miss the step of making sure they’ll be okay. We want sites to be our partners, to collaborate with us, and get our study over the finish line in a timely manner, and yet we forget the most important thing – to take care of them. It’s the little things that are the big things, and when we take time to address the little things, we see big results. When we advocate for the site, we’re advocating for their patients and for the study. It should never be a win-lose. Win-lose gives us short-sighted gains. Sure, we get the study done, but are sites really going to advocate for us? Are they going to be lining patients up in anticipation of your next study, so they can take best care of their patients?

Over 70% of Stiris’ clinical team have worked at the site level and that brings a level of empathy, advocacy and understanding to our team that is appreciated by the sites. We understand their perspective and have lived their challenges, and that gives us an advantage in caring for them.

If you want your study to be a success, and you want to set up your future studies for success, this is where you start. Because, without the sites, you have nothing.

Imagine a scenario where timelines are tight, the pressure is on, and the workload is more than you anticipated. You need more resources to get you through a busy time, and you have to figure out where you’re going to get them, and when. Oh, and then there’s that next thought of ‘what’, what are you going to get? We’ve been there, and we get it. Which is why we strategically designed Stiris to be prepared to deal with these scenarios. From the outset, we organized our team so it may contract and expand as your study requires, without compromising quality or culture. This means you can rapidly resource your study as needed, with team members of the same caliber and expertise as those you already have onboard.

Data base lock? Interim analysis? Sites recruiting faster than anticipated (yes, that does happen, check out this case study)? We’ve got you covered.

Services & solutions

We become an integral and involved part of your team, committed as you are to the success of your clinical trial. We leverage capabilities to increase efficiencies and look for opportunities that present in preparation for or during your study and make them happen.

Rescue

Project Management

Clinical Monitoring

Study Start Up

Medical Monitoring

Auditing

Regulatory Affairs

Global Coverage

CTMS/eTMF

All services & solutions

Uncommon reliability

The Stiris brand is prevalent in everything we do.

Great teams start with astute leadership. Stiris begins by understanding your individual needs, your clinical and commercial objectives, and your strengths and limitations so we can assemble the right expertise to achieve your goals. Since the team will be the primary drivers for the success of your trial, we like you to see what you’re getting from the very beginning. We provide you with CVs and detailed information about the people who will be running your trial. We believe your to-do list should not be burdened with training replacement CRAs or rebuilding site relationships. When you start with the right personnel and plan, leading a team to data lock can actually take fewer of your resources and produce fewer headaches.

Meet our team

At Stiris, we give you:

The very best talent
Clarity and honesty
A proactive, nimble and creative organization
A cooperative, consultative team environment
A committed team from start to finish

Meet our team

We're not your typical CRO

And we have the case studies to prove it.

You’ll be greeted with a handshake by the team that is going to run your project start to finish; we don’t switch out team members once we begin the process. It’s sort of old style, we agree – more like a consulting team – but that’s how we like it. We’re confident you’ll like it too, especially when we hit data lock.

All case studies