Services

CARIMER’s Commitment to you

At CARIMER, we are passionate about the success of our partners. We are a privately-owned organization and can provide both site management organization (SMO) and full-service clinical research organization (CRO) services, depending on your needs.

We do not subscribe to a one-size-fits-all approach to clinical research services that are sometimes seen from larger vendors. Instead, we are committed to working closely with you to ensure that your product has the best chance of success.

With long-term relationships with over 300 sites in South America and the Caribbean, we have access to a diverse population with nearly all medical indications and we can handle any service you may need for your product.

We are experts in feasibility and enrollment forecasting and are committed to providing you with world-class service and on-time delivery. We are uniquely focused on site support and invest in building those site relationships over time. We believe in the work that we do, and our staff's passion for research is what drives us
to new territories.

Management Services Include

Determining site feasibility and qualification according to protocol requirements and finding the ideal site(s) for your study.
Submission to an ethical review board (ERB)—our staff’s intimate knowledge of our local ERBs combined with our efficient personnel makes our turnaround time unbeatably quick.
On-site training of protocol procedures for our investigational team and the study staff
Archiving trial documentation and quality control

Clinical Monitoring Services

We operate via local CRAs in each country in the region to ensure that our clients have immediate access to local knowledge, with robust, centralized SOPs. Source documentation is monitored in a local language, while the CRFs are most typically in English for multinational, multicenter clinical studies. All our CRAs are proficient in English language.

Services include but are not limited to:

Investigator enrollment
Pre-study site evaluation and investigator assessments
Regulatory document preparation and collection
Budget and contract negotiation

Staff training
Documentation maintenance and updates
Site initiation, interim and close-out site visits
Clinical study material accountability

At Carimer, quality assurance is guaranteed. We provide:

An internal QA/QC team
Verification of study compliance to ICH E6 (GCP), applicable laws, study protocols, policies, and Standard Operating Procedures (SOPs) by our dedicated regulatory compliance team which is always up to date on new policies and procedures in the clinical research space.
Audit of investigational sites and clinical trial vendors