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Senior Clinical Research Associate

i-Pharm ConsultingUnited Kingdom🇬🇧United KingdomPosted 20 Aug 2026

Quick Overview

Seniority
Mid Senior
Work mode
Remote
Location
United Kingdom
GCPClinical ResearchClinical TrialsComplianceNursingReconciliation

Job Description

Freelance/Self-Employed Contract | Remote-based with 8 to 10 days onsite per month


We are partnering with a mid-size, fast-growing CRO to find an experienced Senior Clinical Research Associate based in the UK for a freelance contract. This is a great opportunity for a seasoned CRA who wants the autonomy of freelance work combined with the stability of a well-established, growing organisation.


The Role

You'll manage a portfolio of sites, balancing remote monitoring with regular in-person visits (approximately 8 to 10 days onsite per month). You'll take ownership of the full monitoring lifecycle, from site qualification through to close-out, while acting as a trusted point of contact for investigators and site staff.


Key Responsibilities

  • Conduct qualification, initiation, interim monitoring, and close-out visits across assigned sites
  • Perform source document verification, CRF review, and query resolution across paper and EDC systems
  • Ensure ongoing site compliance with ICH-GCP, the UK Medicines for Human Use (Clinical Trials) Regulations 2004 (as amended), and MHRA reporting requirements
  • Identify site-level risks proactively and work with sites to resolve issues before they escalate
  • Review subject safety data and informed consent documentation
  • Maintain accurate, timely documentation and TMF filings
  • Oversee IP accountability, storage, and reconciliation at site level
  • Build and maintain strong relationships with investigators, site teams, and sponsor contacts
  • Balance a mixed remote/onsite model efficiently, managing your own schedule and travel


About You

  • Based in the UK
  • 5+ years' CRA experience, with a strong monitoring track record across multiple sites
  • Confident working independently as a freelancer, with strong self-organisation and time management
  • Comfortable with a hybrid remote/onsite rhythm and regular travel
  • Experience with CTMS and EDC platforms
  • Life sciences, nursing, or related degree/qualification


If you're a self-driven Senior CRA based in the UK, looking for a freelance opportunity with real autonomy, we'd love to hear from you.

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