Senior Clinical Research Associate

Please apply on our imdximc.com career page -

https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=3bd5c297-be43-4cb4-8308-01407875bfa2&ccId=19000101_000001&lang=en_US

Why Join iMDx

At Insight Molecular Diagnostics (iMDx), our mission is to democratize access to molecular diagnostic testing. At our heart, we are a science-driven organization focused on giving clinicians and researchers the diagnostic tools they need to help improve patient outcomes.

Join us and be part of a team that’s redefining what’s possible in healthcare.

Core Competencies

• Site Management & Monitoring Excellence
• Expertise in managing andmonitoringclinical trial sites, including conductingselection, initiation, monitoring, and close-out visits while ensuring compliance with protocols and regulatory requirements. 
• Regulatory Compliance & GCP/ICH Expertise

Strong knowledge and application of clinical research regulations, ensuring adherence to GCP, ICH guidelines, and sponsor expectations tomaintaindata integrity and audit readiness. 

• Clinical Trial Execution & Oversight

Ability to track and manage study progress, including enrollment, regulatory submissions, CRF completion, and data query resolution to ensure successful study delivery. Skilled in delivering protocol training,maintainingclear communication with site personnel, and collaborating with cross-functional teams to drive alignment and resolve issues. Proactively assesses site performance,identifiesrisks or compliance gaps, and escalates issues appropriately while drivingtimelyresolution. 

• Stakeholder Communication & Training
• Risk Assessment & Problem Solving
• Organization, Planning & Results OrientationStrong ability to manage multiple priorities, plan effectively, andmaintainhigh attention to detail while delivering results within timelines and quality expectations. Professional Experience

• Monitor and manage clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations, contributing to high-quality clinical data
• Conduct all site visits (selection, initiation, monitoring, and close-out) in alignment with GCP and ICH guidelines
• Collaborate with site staff to implement and track recruitment strategies aligned with study timelines and enrollment goals
• Deliver protocol and study-specific training to site personnel,maintainingclear and consistent communication to manage expectations and resolve issues
• Evaluate site performance and protocol adherence, escalating quality concerns to ensure compliance and data integrity
• Track study progress, including regulatory submissions, subject enrollment, CRF completion, and data query resolution
• Ensure essential documents are collected,maintained, and audit-ready within the TMF and ISF per regulatory standards
• Document site activities, visit findings, and follow-up actions through detailed reports and correspondence
• Partner with cross-functional teams to support study execution and ensure alignment with project objectives
• Support recruitment planning and site financial activities, including investigator payments and site budget processes

What You Bring To The Table

• Bachelor’s degree in life sciences or a related field;Master’sdegree preferred
• CCRP, CCRA, or ACRP certification preferred
• Minimum of 4 years of clinical trial management experience
• Intermediate knowledge of clinical trial processes, including planning, design, conduct, and execution
• Strong understanding and application of clinical research regulatory requirements
• Broad protocol knowledge with foundational therapeutic area understanding
• Excellent written and verbal communication skills, including strong presentation abilities
• Strong problem-solving and critical thinking skills
• Effective planning, time management, and prioritization abilities
• Ability to organize resources, set clearobjectives, and provide direction to achieve goals
• Proven ability to manage changing priorities and adapt to evolving circumstances

Physical Demands

• Standing, sitting, walking, bending, reaching, manual manipulation, and lifting 25 pounds.
• Ability to have full-body movement
• Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for at least 50% of a typical working day.
• Ability to travel 15% domestically and internationally if required.

Job Scope, Additional Duties, and Employment Status:

This job description is intended to provide a general overview of the position and does not include all duties, responsibilities, or tasks that may be assigned. The scope of this role may change at any time based on organizational needs, business priorities, or operational requirements. Employees may be required to perform additional duties outside of the general scope of this position as assigned.

Employment with the Company is on an at-will basis, meaning either the employee or the Company may terminate the employment relationship at any time, with or without cause or notice, subject to applicable law.

Probationary Period:

Employment is subject to an initial 90-day probationary period, during which performance, conduct, and overall role fit will be evaluated. Continued employment beyond this period is contingent upon satisfactory performance and alignment with organizational expectations.

Why Wait? Apply Today!

At iMDx, every role has a purpose, and every team member plays a part in changing lives. Your skills, ideas, and passion could help shape the future of precision medicine—making life-changing healthcare accessible to people everywhere.

If you’re ready to do work that truly matters, we’d love to hear your story. Join a team of innovators, problem-solvers, and collaborators who turn complex science into clarity and impact.

This is your moment. Don’t wait—apply now and be part of something extraordinary. Together, we can create the future of healthcare.

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Employee assistance program
• Health insurance
• Life insurance
• Paid time off
• Parental leave
• Retirement plan
• Vision insurance

Work Location: Hybrid remote in Nashville, TN 37217