ClinChoice Tech Stack

Full-service CRO delivering clinical development and regulatory services across pharma, biotech, and medical devices

Pharmaceutical Manufacturing Horsham, Pennsylvania 1,001–5,000 employees Founded 1995 Privately Held

ClinChoice operates as a global contract research organization serving pharmaceutical and biotech sponsors across clinical development, regulatory submissions, and post-market surveillance. The tech stack reflects a compliance-heavy, data-centric operation—Vault, SAP, SAS, CDISC standards (SDTM, ADaM), and regulatory-grade tools dominate, with Python adoption signaling a push toward automation in data workflows. Hiring velocity is accelerating across research, healthcare operations, and data roles, while active pain points cluster around artwork approval bottlenecks, regulatory timelines, and process automation—suggesting internal friction around submission readiness and CRO delivery velocity.

Tech Stack 37 technologies

Core StackSAP Wrike SAS Java Python MATLAB Power BI Vault Minitab Microsoft Office Outlook Excel Word PowerPoint R CDISC SQL Git tidyverse R Markdown Shiny CDISC SDTM CDISC ADaM C/C++ SharePoint Windows PLM PDF Veeva HTML+7 more

AdoptingPython

What ClinChoice Is Building

◆Challenges

Inefficiencies in artwork development process
Inefficient artwork approval workflows
Ensuring compliance with qualification activities
Expanding cra network
Increasing closing rates
Regulatory audit preparation
Meeting slas and regulatory timelines
Regulatory submission process improvement
Process automation
Vendor management

▲Active Projects

Adam dataset development
Global regulatory submissions
Phase i oncology trial monitoring
Product license maintenance portfolio delivery
Car t study monitoring
Crf design and development
Implementation of quality control process
Oncology clinical trials
Process improvements for artwork approval workflow
Electronic submission package creation

Hiring Activity

Accelerating100 roles · 50 in 30d

Department

Research

Healthcare

Data

Legal

Ops

Regulatory

Manufacturing

Product

Seniority

Senior

Mid

Junior

Manager

Director

Principal

Lead

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About ClinChoice

ClinChoice is a full-service CRO founded in 1995, headquartered in Horsham, Pennsylvania, with 1,001–5,000 employees. The company provides clinical trial execution, regulatory strategy and submissions, pharmacovigilance, biometrics, and quality/compliance services to sponsors in pharmaceuticals, biotechnology, medical devices, and consumer health. Operating across the Americas, Europe, and Asia-Pacific with active hiring in 15+ countries (United States, India, Philippines, Bulgaria, Mexico, and others), ClinChoice manages end-to-end product lifecycle work, from Phase I oncology trials to post-marketing real-world evidence and regulatory audit preparation. The current project portfolio includes global regulatory submissions, CAR-T and oncology trial monitoring, ADaM dataset development, CRF design, and electronic submission package creation.

HeadquartersHorsham, Pennsylvania

Company Size1,001–5,000 employees

Founded1995

Hiring MarketsBulgaria, Mexico, Belgium, Germany, Netherlands, Brazil, India, United States

Frequently Asked Questions

What tech stack does ClinChoice use?

ClinChoice uses Vault, SAP, SAS, Minitab, CDISC (SDTM, ADaM), SQL, R, Python, MATLAB, Veeva, Power BI, and Wrike for clinical data management, regulatory submission, statistical analysis, and project tracking across its CRO operations.

What is ClinChoice working on?

Active projects include global regulatory submissions, Phase I oncology trial monitoring, CAR-T study monitoring, ADaM dataset development, CRF design, electronic submission package creation, and process improvements for artwork approval and quality control workflows.