Clinical Research Coordinator, Ripley TN

Job Description

Job Description

Benefits:

• Competitive salary
• Dental insurance
• Health insurance
• Paid time off
• Training & development

Benefits:

• Competitive salary
• Dental insurance
• Health insurance
• Paid time off
• Training & development

Clinical Research Coordinator (Part time/Full Time)

About Us
We are an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role. 

Role Overview
Here's an opportunity to work for a dynamic and growing clinical research company. We have a fantastic and supportive work environment. The Clinical Research Coordinator plays a pivotal role in managing and overseeing clinical trials, ensuring compliance with regulatory requirements, and facilitating the smooth operation of research studies. This position works on-site at the physician’s practice. This position requires a detail-oriented individual with a strong background in medical terminology, data management, and clinical trials management. The ideal candidate will have at least one year of experience coordinating all aspects of clinical research projects from initiation to completion. Phlebotomy skills required.  

Key Responsibilities

• Manage the day-to-day operations of clinical trials, ensuring adherence to protocols and timelines. 
• Analyze data collected during trials and maintain accurate records for compliance management. 
• Oversee blood sampling procedures and ensure proper handling and documentation. 
• Train on clinical trial protocols and procedures. 
• Collaborate with healthcare professionals to ensure participant safety and integrity of data. 
• Utilize software for data capture and reporting 
• Maintain knowledge of medical terminology to effectively communicate with team members and stakeholders. 
• Ensure compliance with ethical standards and regulatory requirements throughout the research process. 

Required Qualifications

• Clinical experience preferred but not required 
• Experience in clinical trials - 2+ years of coordinator experience 
• Proficiency in data entry 
• Knowledge of medical terminology relevant to clinical research. 
• Phlebotomy and blood sampling techniques is required 
• Patient Recruitment experience required 
• Excellent organizational skills with attention to detail and the ability to manage multiple tasks simultaneously. 
• Travel and work required between two sites in Jackson TN (2 days) and Ripley TN (3 days). 

What We Offer 

• A mission-driven and collaborative team culture. 
• Opportunities for career growth as the company scales. 
• The chance to contribute meaningfully to expanding access to clinical research for underserved populations. 

If you’re looking for an opportunity to take ownership, build something from the ground up, and make a significant impact, we’d love to hear from you! 

Medovation Clinical Research is an Integrated Clinical Research Organization dedicated to expanding access to clinical research and empowering physicians to bring advanced care options closer to diverse patient communities. We pride ourselves on fostering a collaborative and honest work environment where every team member takes ownership of their role. We value impactful work, open collaboration, and a spirit of diversity and inclusion.