clinical trial program development
At TrialNAV, our goal is to help build and develop site research programs to improve patient access to clinical trials.
Due to our extensive cross-coverage expertise, we understand the unique & complex site programmatic challenges and are equipped to provide concrete and effective solutions for you.
Our Site Solutions
We provide a no obligation, complimentary gap analysis of your research program.
Administrative Startup
- Streamline administrative startup processes including regulatory, legal, finance, etc.
- Trial portfolio management
- Budgeting and financial forecasting
- Referrals to new study opportunities
- Committee setup (eg. feasibility, scientific, DSMB, IRB)
- Research educational training
- Marketing and recruitment strategies
Clinical Coordination
- Trial to staffing acuity
- Resources and equipment evaluation
- Trial coordination workflow review
- Training & continuous education of both research and ancillary team members
- Investigator training
- Staff management: harmonize job descriptions and career development pathways
- SOP creation and review
Growth & Expansion
- Strategic partnerships
- Multi-centered network site management
- Research program development (eg. Phase I unit, research lab, tissue bank, research infusion unit, cell therapy lab)
- Performance metrics and analytics
- Quality management program development
- Revenue cycle management & budget forecasting
- Business development
Digital Transformation
- Screening & enrollment platforms
- Marketing and referrals
- Population querying
- CTMS evaluation
- Staffing forecasting
- Finance, regulatory, quality management, audit readiness, coordination, patient facing, and investigational pharmacy tools
Our team is backed by up to 25 years of oncology clinical trial experience in research site management, direct research patient care, CROs, SMOs, pharmaceutical biotechnology, and research technology platforms.