Contract CRA / Senior CRA - West Coast, USA

Contract: 12 months
Start Date: December 2026
Location: US West Coast
Employment: W2 Contract
Therapeutic Area: Respiratory / Asthma and/or Dermatology
Study Phases: Phase II & Phase III

Role Overview

We are supporting a client seeking an experienced Clinical Research Associate (CRA) / Senior Clinical Research Associate (SCRA) to support a high-profile clinical development programme.

The successful candidate will have strong clinical monitoring experience across Phase II and Phase III studies, with previous therapeutic experience within Respiratory, Asthma and/or Dermatology.

This role would suit an experienced CRA/SCRA who is comfortable working closely with investigational sites and wider clinical study teams throughout the lifecycle of a clinical trial.

Key Responsibilities

• Perform clinical trial monitoring activities across Phase II and Phase III studies
• Build and maintain effective relationships with investigation sites and study teams
• Support sites throughout the clinical study life-cycle
• Monitor sites to ensure study activities are being performed in accordance with the clinical trial protocol
• Review study documentation and support the identification and resolution of site-level issues
• Work closely with the wider clinical study team to maintain effective communication across assigned sites
• Support the quality and integrity of clinical trial activities
• Track site progress and escalate relevant study or site issues when required
• Maintain accurate and timely monitoring documentation
• Support the successful delivery of assigned clinical studies and programmes

Essential Requirements

• Previous professional experience as a CRA or Senior CRA
• Based on the US West Coast
• Strong Phase II and Phase III clinical trial experience
• Previous clinical trial experience within at least one of the following:
  • Respiratory
  • Asthma
  • Dermatology
• Experience working directly with investigation sites and clinical study teams
• Strong understanding of clinical trial monitoring and site management
• Strong communication, organisation and stakeholder-management capabilities
• Able to work effectively within a cross-functional clinical study environment
• Available for a 12-month contract
• Able and willing to work on a W2 basis
• Available for an anticipated December 2026 start