Freelance Clinical Research Associate (CRA) - Remote

About the Role

We are seeking a Freelance Clinical Research Associate (CRA) - Remote to ensure effective monitoring of clinical trials, focusing on remote monitoring and supporting a major trial across multiple US sites. As a CRA, you will play a crucial role in overseeing the progress of clinical trials and ensuring compliance with regulatory standards.

What You'll Do

• Ensure effective, risk-proportionate monitoring of clinical trials.
• Support a major trial across 15+ US sites involving over 7,000 patients.
• Prepare, conduct, and report on monitoring visits.
• Work autonomously within a lean team structure.
• Interface directly with Trial Managers to ensure smooth operations.
• Focus on remote monitoring with some onsite visits as necessary.
• Collaborate with Clinical Operations, Product, and Commercial teams to align on project goals.
• Develop monitoring plans and strategies to enhance trial efficiency.
• Maintain high monitoring standards as our customer base grows.
• Work in a startup environment, contributing to innovative solutions in clinical trials.

Requirements

• 3+ years of independent site monitoring experience.
• Experience with remote monitoring and decentralized clinical trials (DCT).
• Strong knowledge of Good Clinical Practice (GCP), Good Distribution Practice (GDP), and regulatory requirements.
• Attention to detail and excellent communication skills.
• Ability to work autonomously and proactively in a fast-paced environment.
• Experience in developing monitoring plans and strategies.
• A bias to action and creativity in problem-solving.
• Familiarity with clinical trial regulations is essential.
• Experience in a startup or early-stage environment is advantageous.
• Excitement about shaping clinical trial technology and processes.

Nice to Have

• Previous experience in managing multiple clinical trials simultaneously.
• Familiarity with electronic data capture systems.
• Experience in a variety of therapeutic areas.

What We Offer

• Work on high-impact clinical trials that make a difference.
• Collaborate with industry-leading teams and experts.
• Enjoy flexible scheduling to balance your work-life needs.
• Competitive contractor rates based on experience.
• Leverage established infrastructure and resources to support your work.
• Work with a stable, well-funded organization committed to innovation.
• Contribute to meaningful research that advances healthcare.
• Receive comprehensive support from the Clinical Operations team.
• Flexibility of working as a contractor with the potential for future opportunities.