Comprehensive Clinical Research

Service managing payments to clinical trial sites and investigators.

End-to-end biostatistics and programming support ensuring rigorous study design, accurate analyses, and regulatory-compliant datasets for successful submissions.

Everest Clinical Research provides flexible, high-quality biostatistics and programming support through both project-based work and Functional Service Provider (FSP) staff augmentation models for a global pharmaceutical company.

A comprehensive clinical operations service including regulatory submission support, TMF management, data management, biostatistics and statistical programming, and pharmacovigilance for a Phase III rare disease biotech study.

Everest Clinical Research offers personalized clinical operations and project management services with expertise and infrastructure to manage complex studies, providing full-scope or tailored services from feasibility through close-out.

Everest Clinical Research took over two Phase III oncology studies from a larger global CRO, providing full-service clinical trial management including data management, biostatistics, statistical programming, site operations, drug safety, IRT, biometrics, pharmacovigilance, and depot management to complete the studies on time.

BioNote® is Everest’s subject-facing app designed to simplify eDiary and ePRO completion for study participants, supporting both BYOD and provisioned device models with an intuitive interface and proactive notifications to boost compliance and engagement.

Provided to backfill internal team attrition and support exploratory programming for scientific conferences.

Everest's in-house eCOA platform combines patient-friendly technology with dedicated study monitors and 24/7 support, delivering both the platform and hands-on service for clinical trials.

A customizable eCOA system supporting validated instruments, diaries, dosing compliance, and hybrid BYOD models, backed by a proactive support team from first site activation to study closeout.

An AI-embedded solution that helps streamline the management, standardization, and analysis of study data in real-time, resulting in accelerated data collection and enhanced data quality with robust data visualization capabilities.

Biometrics and IWRS support services provided by Everest Clinical Research for a large-scale, global Phase III respiratory trial with 16,000 patients across 26 countries, resulting in zero FDA and EMA inspection findings.

Support for regulatory and Institutional Review Board submissions in clinical trials.

Services combining proactive risk assessment with data analytics to optimize trial oversight, enhance data integrity, and focus resources where they matter most.

Integration tool enabling streamlined case intake and seamless data flow between EDC systems and Argus Safety Database.

Robust and scalable platform for case management and regulatory reporting in pharmacovigilance and drug safety.

A clinical data dashboard solution that integrates data across clinical trial systems including EDC, IWRS/IRT, eDiary, CTMS, and other third-party data capture systems to provide a centralized data review portal with custom visualizations and role-based access controls.

A proprietary 21 CFR Part 11 compliant web portal providing secure, auditable, and user-friendly access to DMC documents for clinical trial oversight.

Monitoring visits conducted on-site or remotely to ensure trial compliance and data integrity.

Monitoring services including central and risk-based approaches to ensure trial quality and compliance.

Management of clinical trial sites to ensure compliance and operational efficiency.

Management of the trial master file to ensure proper documentation and compliance.

Medical Monitoring services include globally accessible medical experts, seamless sponsor collaboration, and data-driven management that ensures patient safety across all phases of clinical development.

Supported development of clinical and regulatory documents.

Designed and implemented a program that included routine data reviews focused on pediatric safety, quarterly literature reviews, alignment with DSMB data to detect trends, safety signals, and identify needed improvements.

Management of vendors involved in clinical trials to ensure quality and timely delivery.

Services to assess feasibility and select appropriate sites for clinical trials.

Secure portal for real-time SUSAR notifications to investigators and tracking acknowledgements.

Audits conducted at clinical trial sites to ensure quality and compliance.

Sourcing of local drugs and equipment needed for clinical trials.