End-to-End Clinical Trial Support & Functional Service Provider Solutions
IPS delivers flexible clinical trial support, FSP solutions, and in-house staffing to help sponsors streamline operations, improve study performance, and accelerate time to market. Our experienced clinical research teams support every phase of the trial lifecycle with scalable, cost-effective solutions tailored to your program.
Clinical Support Capabilities
- Feasibility Assessments
- Site Identification & Selection
- Protocol Development
- Study Startup & Rescue Studies
- Patient Recruitment & Site Engagement
- Clinical & Medical Monitoring
- Pharmacovigilance / Drug Safety
- eTMF & Document Management
- Supply Chain Management
- Therapeutic Area Expertise
Therapeutic Areas Supported
IPS supports clinical trials across a wide range of therapeutic areas, including:
- Oncology
- Neurology / CNS
- Dermatology
- Hematology
- Ophthalmology
- Rare Disease
- Immunology
- Cardiology
- Gastroenterology
- Endocrinology
- Medical Device
- Cell & Gene Therapy
Improving the Clinical Trial Experience
Our collaborative approach gives sponsors direct access to senior clinical experts, experienced project teams, and integrated operational support. IPS helps organizations improve trial quality, increase flexibility, and bring therapies to market faster.
Why Sponsors Choose IPS
- Strategic clinical trial consulting and scientific expertise
- Agile, scalable FSP and staffing solutions
- Strong governance, communication, and KPI tracking
- Accurate feasibility planning and rapid adaptation
- Therapeutic area expertise and precise patient recruitment
- Real-time data visibility and transparent communication
- DOD-level data security and quality-focused operations
Clinical Trial Consultation & Strategy
- IPS works closely with sponsors to define study goals, evaluate feasibility, optimize budgets and timelines, and identify operational risks before launch. Our experienced project teams provide strategic guidance to support faster enrollment, improved site performance, and efficient clinical execution.
- What You Can Expect
- Experienced clinical project leadership
- Strong site relationships and recruitment strategies
- Flexible operational support for complex studies
- Streamlined communication and data flow
- Compliance with global regulatory requirements
- Scalable solutions for centralized and decentralized trials
- What You Can Expect
Clinical Staffing & FSP Solutions
- IPS identifies, recruits, and manages experienced clinical research professionals, including Project Leaders, Clinical Research Associates (CRAs), and Client Delivery Directors. Our scalable staffing model supports both centralized and on-site programs.
- Staffing Benefits
- Flexible and scalable talent acquisition
- Consistent training and low turnover
- Dedicated therapeutic area expertise
- On-site and in-house support capabilities
- Long-term partnership approach focused on study success
- Staffing Benefits
Implementation & Ongoing Program Management
- Our implementation model includes dedicated leadership, compliance oversight, change management, and operational optimization to ensure long-term program success.
- Ongoing Operational Support
- Lean and Six Sigma workflow optimization
- Sponsor engagement and program oversight
- Secure data management and disaster recovery
- Staff onboarding, training, and development
- Portfolio and resource management
- Single point of contact for seamless communication
- Ongoing Operational Support
