Services

Contract Research Organization Services for Clinical Trials

At Evoclinical, we are committed to transforming clinical trial insights into actionable strategies you can trust; building an innovation-driven Contract Research Organization (CRO) that stands at the forefront of clinical research statistics & data management.

CRO expertise you can trust

We are a Contract Research Organization with expertise that encompasses the planning and analysis of clinical trials. This includes statistical consulting, biostatistics, programming, data management, medical writing, clinical trial feasibility analysis and regulatory support services.

Additionally, we extend our capabilities to registries, diagnostics, publication support, and exploratory analyses of medical databases. We use data-mining methods suitable for “large messy data”, ensuring comprehensive support for both pharmaceutical & biotech companies and investigator-initiated studies.

What we offer

Contract Research Organization Services

Statistical Consulting

We provide clinical trial design and statistical guidance in short order. Be it interpreting concerns from a regulatory authority, endpoint selection, efficient study design features, handling intercurrent events, cost and timeline reduction, or providing Competitive Landscape Analysis, to name but a few.

Statistical Analysis

EvoClinical provides statistical services for clinical trials. This includes analysis plans, CDISC-compliant data sets, tables, listings, figures, randomization setup, interim and final analyses, safety summaries, integrated safety and efficacy summaries, clinical study report reviews, and full submission support.

Clinical Study Design

New product indication, target population, mechanism of action, and regulatory pathways are used to research and recommend study design options that will efficiently answer research questions while meeting regulatory requirements and expectations and business constraints.

Regulatory Support

EvoClinical supports regulatory submissions by preparing data packages, TFLs, and briefing materials. Statisticians join sponsor teams to answer authority questions, attend meetings, draft responses, and ensure study designs meet regulatory standards. Our expertise helps sponsors avoid flawed designs and keep preferred study options open.

Data Management

EvoClinical’s data management team supports clinical trials with eCRF setup, testing, training, logic checks, query handling, medical coding, and data review. We manage study metrics, database locks, lab ranges, and site support to ensure data are accurate, complete, and analysis-ready while meeting regulatory and protocol requirements.

Statistical Training

EvoClinical offers custom statistical training to help sponsor teams better understand clinical research statistics. Topics to consider are protocol writing or interpretation, purpose and benefit of study design features, analytical methods like hypothesis testing and missing data adjustment methods, and results interpretation.

Medical Writing

EvoClinical medical writers are qualified to write documents for submission to regulatory authorities. Including study protocol, clinical study reports, informed consent forms. Medical writers also prepare manuscripts, conference abstracts and posters, advisory board minutes & summaries, and perform systematic literature reviews.

Clinical Trial Feasibility Analysis

De-risk study design and shorten start-up timelines! Our Clinical Trial Feasibility Analysis converts global registry data into dashboards that benchmark protocols (i.e., support feasibility scoping, estimate recruitment timelines, sample size, phase, number of sites, etc.), pinpoint top investigators, and optimize site selection.

Contact us

Partner with a BioStatistics CRO you can trust.

Our process helps put you at ease when purchasing statistical services

Whether you’re facing a mid-program regulatory change, complex study design questions, or need transparent statistical methodology that can withstand regulatory scrutiny, EvoClinical’s biostatistics team is ready to help.

Focus areas:

What happens next?

1

Schedule a call

2

Discovery Conversation

3

We prepare a proposal

Schedule a Free Consultation

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