If you are a researcher exploring investigator-initiated research, studies or trials – we can help.  The Celéri Explorer Research Group will assist you with optimal study design to achieve your protocol’s objectives while ensuring fast study readiness.  Through our robust electronic data capture, you can collect study participant data via electronic Case Report Forms (eCRF), clinical logs and integrations with wearables, smart scales, etc.  Most importantly, we are experts in electronic Patient Reported Outcome (ePRO) development.  Use our existing library of already available PRO assessments or we can assist you with custom design of questionnaires tailored for your study’s needs.  Finally, we bring site management to the table with ready site access to over 350 pain network providers and AI-based patient recruitment capabilities.

If you are a Sponsor, we offer a full range of trials….IDE to post-market studies… for the advanced support of your device or therapeutic.

Our depth of clinical registry experience allows us to give you the irrefutable data and insights you need so you can be confident in meeting RWD requirements.

The fact that we have a ready-consortium of partners in our Research Group allows you to customize your contract to include only the services needed:

Greenlight Guru Clinical

Greenlight Guru Clinical (formerly SMART-TRIAL) is a single, compliant platform for collection and management of all clinical evidence, safety, and performance data.

• Designed for MedTech efficiency and growth
• Pre-validated for FDA & ISO 14155:2020
• Collect clinical evidence from physicians, patients, and other end users
• Built-in templates and clinical builder

Clinical Research Strategies

Clinical Research Strategies is a Pittsburgh, PA-based contract research organization and executive management consultancy for start-up and mid-size life sciences companies. We help instill fiscal discipline and reduce risks in clinical development, corporate affairs, and quality assurance programs. Project-specific, fit-for-purpose, ad hoc consulting, and staffing clinical trials is what we do best, whatever stage your program is in. CRS advisors have been everywhere – clinical research organizations, life science start-ups, and large pharma and medical device companies. We can help you manage and overcome complicated trial operations and the burdensome regulatory pathways to a successful product launch.

Other services:

• Statistician
• Pharmacovigilance Consulting
• Pain Network Access (+250 ready-investigators)
• KOL pairing
• PainRWD™ Science Cloud (+220k pain cases with outcomes and a deep data dictionary (e.g. concomitant meds, conditions, social history, interventions/procedures, and more) access for control group use or observational study design.

Talk to our research team to learn more about our Group.