Freelance CRA (Clinical Research Associate)

TL;DR

Freelance CRA (Clinical Research Associate): Ensure risk-proportionate monitoring of hirify.global’s US clinical trials, with primary emphasis on remote monitoring and end-to-end site lifecycle support. Focus on building monitoring plans, conducting and reporting all monitoring visit types (from site selection through close-out), and partnering with Trial Managers while contributing to the Citrus central monitoring platform.

Location: Remote (US)

Company

hirify.global powers faster, more reliable clinical trials to help new treatments reach patients sooner.

What you will do

• Act as primary contact for end-to-end site lifecycle support for a major trial across 15+ US sites.
• Write Monitoring Plans and arrange, conduct, and report monitoring visits (primarily remote) from SIV through close-out.
• Coordinate monitoring activities and deliverables autonomously, identifying and managing issues and advising Trial Managers on process improvements.
• Perform central monitoring through the Citrus platform, reviewing data trends and anomalies.
• Collaborate with Clinical Operations, Product, Commercial, and sponsor-side teams to support monitoring strategy.
• Provide input to help design and shape the Citrus trial monitoring platform.

Requirements

• Location: Must be based in the US
• 3+ years of independent site monitoring experience across all monitoring visit types (site selection, SIV, IMV through close-out).
• Experience developing strategies for effective remote monitoring.
• Experience with Decentralized Clinical Trials (DCT) and central monitoring approaches, including reviewing and reporting data trends and anomalies.
• Strong working knowledge of GCP/GDP and regulatory requirements, with awareness of potential regulatory changes.
• Ability to review and develop monitoring plans and communicate confidently with internal and external stakeholders.

Culture & Benefits

• Flexible scheduling and project variety as a contractor.
• High-impact, mission-driven work focused on improving patients’ lives.
• Lean team structure with autonomy and direct collaboration with Clinical Operations.
• Comprehensive support from the ClinOps team.
• Competitive contractor rates.

Hiring process

• 15-minute initial conversation with the ClinOps Talent Partner.
• 30-minute technical/functional interview with members of the CRA team, including a deep dive into experience and approach to key challenges.