Remote Clinical Research Associate (Arizona Trials)

Description

Remote Clinical Research Associate (Arizona Trials)

Make a Real Impact from Anywhere

Can your organizational instincts and scientific rigor drive breakthroughs in human health? As a Remote Clinical Research Associate (CRA) for Arizona-based clinical trials, you'll do more than monitor sites—you'll ensure that ethical, accurate, and timely data translates into life-changing treatments. This role isn't about checklists. It's about owning timelines, safeguarding patient experiences, and helping build the future of clinical science—from wherever you thrive best.

What You'll Help Achieve

You'll be the critical connector between investigational sites, clinical teams, and regulatory standards. Your role will power the accuracy and momentum of each Arizona-based trial. By supporting trial protocols, tracking compliance, and advising coordinators, you'll reduce delays and enable safer, faster progress toward new therapies. We trust your expertise to make decisions that matter and empower patients with every milestone.

Key Responsibilities That Drive Results

  • Oversee multiple Arizona trial sites remotely, ensuring protocol adherence and regulatory compliance
  • Conduct virtual monitoring visits, using electronic data capture systems and remote collaboration tools to verify source documentation and case report forms
  • Serve as the go-to resource for site coordinators and investigators—your clarity and confidence help avoid missteps before they happen
  • Identify risks early and act swiftly to resolve queries, deviations, or site performance issues
  • Deliver feedback that improves site performance without creating friction
  • Track patient enrollment metrics and proactively flag timeline risks
  • Support safety event reporting in coordination with clinical teams, regulatory affairs, and medical monitors
  • Collaborate with cross-functional teams across timelines, time zones, and trial phases to ensure high-quality execution

Tools That Power Your Work

We use a robust tech stack that empowers seamless remote work. You’ll use:

  • Veeva Vault eTMF for document tracking and real-time access
  • Medidata Rave and REDCap for EDC and patient data capture
  • Zoom, Slack, and Notion to maintain cross-team clarity and momentum
  • Jira to track trial workflows, including enrollment and data query resolution

You’ll spend less time toggling between tools and more time focusing on what moves research forward.

How We Work Together

We’re a purpose-driven remote team grounded in transparency and trust. You’ll join weekly alignment calls, lead site engagement check-ins, and shape your schedule to prioritize deep work. Need to work early mornings or shift around family commitments? We’re flexible and focused on outcomes, not hours. Our culture is built for focus, feedback, and growth.

What Sets You Apart

  • You’ve monitored Phase I-III clinical trials and are fluent in GCP, ICH, and FDA/EMA guidelines
  • You simplify complexity, whether you're coaching a new site coordinator or presenting trial updates to senior leaders
  • You’ve used remote collaboration tools to foster cross-site alignment and maintain trial integrity
  • You notice what others miss: subtle data patterns, overlooked compliance gaps, and unspoken site concerns
  • You treat patient data with the sensitivity and accuracy it deserves

Minimum Requirements

  • 2+ years as a Clinical Research Associate, with remote or decentralized trial experience
  • Based in or near Arizona, with deep familiarity with the local trial landscape
  • Bachelor’s degree in life sciences, nursing, public health, or related field
  • Comfortable navigating EDC systems, eTMF platforms, and cloud-based documentation workflows
  • Excellent written and spoken communication skills—you adapt your tone for IRBs, sites, and stakeholders

Compensation and Benefits

We believe in recognizing your work and providing you with the space to thrive. This full-time remote role offers an annual salary of $86,551, along with:

  • Generous paid time off and flexible hours
  • Paid certification renewals and professional development stipends
  • Health, dental, and vision coverage
  • Team offsites (virtual and in-person)

Ready to Advance Human Health from Anywhere?

If you're ready to champion research integrity, streamline site success, and shape therapies that change lives, we’re prepared to meet you. Let’s build something meaningful—apply today.