Vanguard Clinical
Vanguard Clinical is a small, diverse, and experienced contract research organization (CRO) dedicated to providing white glove service in clinical development. Founded in 2012 and headquartered in San Diego, CA, it specializes in tailored solutions across various therapeutic areas, including Rare Disease, Early Phase Oncology, and CNS. The company emphasizes transparency, flexibility, and integrity, offering scalable services from individual roles to full-service CRO support, with a focus on small to mid-size sponsors. Vanguard Clinical aims to redefine the CRO experience through personalized, dedicated teams and innovative, scalable solutions.
Industries
Nr. of Employees
medium (51-250)
Vanguard Clinical
Solana Beach, California, United States, North America
Services
Dedicated CRA oversight, site concierge services, conduct of monitoring visits (pre-study, initiation, routine, close-out), and real-time risk mitigation and reporting.
Subject matter experts providing hands-on training, OR procedural oversight, and protocol compliance for device or complex IP administration.
Full-service trial management including dedicated clinical teams, CRO oversight, project recovery, and management of traditional, hybrid, and decentralized trials.
CDMS setup and integrations, data cleaning, database lock, site data entry support, medical coding, and biostatistical services including CDISC/ADaM implementation and TFL production.
Preparation of regulatory documents (e.g., investigator brochures, clinical study reports) and scientific communications for conferences and publications.
Tailored recruitment strategies leveraging market analysis, digital outreach, community engagement, patient registries, and partnerships to optimize enrollment.
Dedicated CRA oversight, site concierge services, conduct of monitoring visits (pre-study, initiation, routine, close-out), and real-time risk mitigation and reporting.
Subject matter experts providing hands-on training, OR procedural oversight, and protocol compliance for device or complex IP administration.
Full-service trial management including dedicated clinical teams, CRO oversight, project recovery, and management of traditional, hybrid, and decentralized trials.
CDMS setup and integrations, data cleaning, database lock, site data entry support, medical coding, and biostatistical services including CDISC/ADaM implementation and TFL production.
Preparation of regulatory documents (e.g., investigator brochures, clinical study reports) and scientific communications for conferences and publications.
Tailored recruitment strategies leveraging market analysis, digital outreach, community engagement, patient registries, and partnerships to optimize enrollment.
Expertise Areas
- Clinical trial management
- Clinical monitoring and site management
- Clinical data management
- Biostatistics and biometrics
Key Technologies
- Clinical trial management systems (CTMS)
- Clinical Data Management Systems (CDMS)
- Electronic Trial Master File systems (eTMF)
- Standardized medical coding dictionaries (e.g., MedDRA, WHODrug)