Clinical Trials Associate

Role overview

CovarsaDx is hiring a Clinical Trials Associate to support the execution of clinical studies within a fast-moving, mission-focused environment. The organization is a CRO specializing in in vitro diagnostic (IVD) and medical device trials, and it works with clients to build study approaches that can adapt quickly when trial needs change. The team emphasizes regulatory achievement, strong clinical research quality, and practical support from experienced research professionals.

In this remote position, you will collaborate closely with Clinical Research Associates and cross-functional partners to keep studies organized, compliant, and progressing on schedule. The role offers exposure to several areas of clinical operations, including site support, documentation, and study coordination, while contributing to work that helps advance diagnostic solutions for patients.

This opportunity is designed for a detail-oriented clinical research professional who enjoys balancing documentation, coordination, and site interaction. It suits someone who is proactive, organized, and eager to build experience in a high-accountability, collaborative clinical operations setting.

What you will do

• Assist the lead study CRA with day-to-day study execution.
• Support remote site monitoring activities, including site initiation, ongoing monitoring, and close-out coordination.
• Check regulatory files, consent materials, and study documentation for completeness, correctness, and compliance.
• Help maintain the trial master file and site-specific records.
• Monitor investigational product tracking and support communication and reporting with study sites.
• Work with internal teams and external sites to keep projects moving smoothly.

What the employer is seeking

• A bachelor’s degree is required, ideally in a scientific field.
• At least 2 years of experience in clinical research or clinical trial management is preferred.
• Strong abilities in organization, communication, and documentation.
• Working knowledge of GCP, ICH, FDA expectations, and clinical trial workflows.
• Comfort working independently in a remote setup while handling multiple priorities.
• Proficiency with Microsoft Office and similar business applications.

Why this role stands out

You will contribute to the operational quality behind clinical studies that can improve patient care. Your work will support site readiness, document quality, and overall trial execution throughout the study lifecycle. Success in the role means staying on top of multiple priorities, building effective relationships with internal stakeholders and study sites, maintaining strong documentation standards, and approaching daily tasks with initiative and practical problem-solving.

Job details

This is a full-time remote role in clinical operations. Compensation is listed at $60,000 to $75,000 per year, depending on skills and experience. Limited travel of up to 10% is required.

Application instructions

Candidates should send a resume and cover letter to Human Resources at hr@covarsadx.com.

Benefits

• Medical, dental, and vision insurance
• Life insurance, short-term disability, and long-term disability coverage
• 401(k) plan with company match
• Paid time off, sick leave, and holiday pay