Clinical Research Associate I (Medtech)

TL;DR

Clinical Research Associate I (Medtech): Monitoring clinical trial sites and managing site activities for biotech, medtech, and pharma projects with an accent on regulatory compliance and data integrity. Focus on ensuring successful delivery of medical innovations and maintaining high standards of patient safety and protocol adherence.

Location: Must be based in the US East Coast (NY, FL, NJ, PA, OH, DC, MD)

Company

A global clinical research organization dedicated to transforming breakthrough science into life-changing medicines and medical devices.

What you will do

• Monitor clinical trial sites to ensure compliance with protocols and regulatory requirements.
• Manage site activities and maintain strong relationships with clinical investigators.
• Verify clinical data accuracy and ensure timely reporting of study progress.
• Collaborate with cross-functional teams to support the successful delivery of clinical trials.
• Contribute to the improvement of clinical monitoring processes and site management strategies.

Requirements

• Must be based in the US East Coast (NY, FL, NJ, PA, OH, DC, MD).
• Experience in clinical research or site management.
• Strong understanding of clinical trial regulations and guidelines.
• Excellent communication and organizational skills.
• Ability to work effectively in a remote, distributed team environment.

Culture & Benefits

• Commitment to professional growth and skill development.
• Flexible work environment designed to support work-life balance.
• Opportunity to contribute to life-saving medical innovations.
• Inclusive culture that values diverse perspectives and individual contributions.