The CRP Legacy
serving Philadelphia for 30 yearsCRP is a dedicated clinical research site at the forefront of clinical research, partnering with industry leaders to improve patient outcomes.
Patient-centric, sponsor-aligned
Focus on diversity
Our staff and our enrollment reflect the community we serve. See the breakdown of who's enrolled in our trials this past year below.
Embracing technology
Our fully electronic Clinical Trial system allows us to minimize administrative burden and streamline operations so our team can focus more on patient engagement and protocol adherence.
Patient centricity
Our participants are the reason we come to work every day. Our decisions and daily processes are guided by the principle that participants will always be the heart of our work.
Clinical expertise
We are proud of our committed research team, most of whom have been with our site for over 15 years. Our cohesiveness as a team and our collective experiences enable us to develop innovative solutions for the complex needs of our clinical trials.
Diversity in our enrollment
Aggregate participant demographics across all studies since 2021, from our clinical trial management system. Based on 2,010 participants with race reported.
Race & Ethnicity
Source: CRP clinical trial management system, 2021 to date. n = 2,010 participants with race reported. Last reviewed July 2026.
What sets us apart
Why participants choose CRP
Free Transportation
Every participant gets free rideshare to and from study visits. No car needed, no cost to you.
Compensation for Your Time
Participants receive payment for every visit, plus access to investigational treatments at no cost.
Two Convenient Locations
State-of-the-art facilities in Philadelphia and Pennington, NJ with free parking and flexible scheduling.
Two facilities. Six capabilities. One standard.
State-of-the-art research sites in Philadelphia, PA and Pennington, NJ — both staffed and equipped to handle Phase II–IV trials end-to-end, with dedicated sponsor and monitor workspace.
Tech-Forward Operations
Fully electronic CTMS (CRIO) plus a custom BigQuery and agent-driven analytics layer powering live dashboards. No paper trail to chase, no double entry.
Specialized On-Site Equipment
FibroScan, ultrasound, centrifuges, EKGs, infusion pumps, and incubators on premise — most studies need no off-site vendors.
IP Storage & Monitoring
Temperature-controlled ambient, refrigerated (2–8°C), and frozen (-20°C / -80°C) investigational product storage with 24/7 alerting.
Patient Comfort & Safety
Private exam rooms, on-campus urgent care, free parking at both sites, and free rideshare to and from every visit for all participants.
Community-Reflective Staff
Our team mirrors the patient populations we serve, building trust with participants and reducing screen failure and dropout.
Sponsor-Ready Workspace
Dedicated monitor workstations, sponsor conference and training room, private investigator and coordinator offices, and a sample processing & shipping lab.
Physical Features
- 3 fully equipped exam rooms
- 3 investigator offices
- 5 offices for coordinators
- 3 private workstations designated for monitors
- 2 in-office bathrooms for patients & specimen collection
Annually calibrated medical equipment includes:
- Secure IP storage area with:
- Temperature-monitored refrigeration (2–8 degrees)
- Temperature-monitored freezers (-20 / -80 degrees)
- Temperature-monitored, controlled, and secured drug storage room
- Sample processing lab
- Phlebotomy and nurses stations
- Centrifuges
- EKG machines
- Incubator
- 2 ultrasound machines
Meet the experts
Leadership

Aneesh Vaze

Liz Usmiani

Leticia Donato

Jeehan Choudhary
Principal Investigators

Eugene Andruczyk

Vinod Rustgi

Brian Shaffer

Lolita Vaughan

Michael Tomeo

Taher Modarressi

Lawrence Leventhal

Joseph Heether
Sub-Investigators

Hal Ganzman
Clinical Research Coordinators

Angelina McMullen

Stacey Scott

Mario Castellanos

Ruby Pereira

Cady Chilensky
Remote Coordinators

Nice Jain

Huzaif Qazi

Aditi Chorage

Siddhesh Mhatre

Kajal Kesharvani

Aadil Ansari
Clinical Research Technicians

Wendy Seidman

Angel Arroyo
Accreditations and Oversight
FDA Regulated
All studies conducted under FDA oversight with Investigational New Drug authorization.
IRB Approved
Every protocol reviewed and approved by an independent Institutional Review Board before enrollment begins.
HIPAA Compliant
Patient data protected under strict HIPAA privacy and security standards at every stage of the research process.
The people behind the research
Get to know the dedicated team at Clinical Research Philadelphia.