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Clinical Research Coordinator, Ripley TN

Medovation Clinical Research LLC

Ripley, TN

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JOB DETAILS
SKILLS
Clinical Medicine, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Data Analysis, Data Collection, Data Entry, Data Management, Data Quality, Dental Insurance, Detail Oriented, Documentation, Health Insurance, Healthcare, Maintain Compliance, Medical Terminology, Multitasking, Operations Research, Organizational Skills, Phlebotomy, Record Keeping, Records Management, Regulatory Compliance, Regulatory Requirements, Sales Closing Skills, Team Player, Training/Teaching
LOCATION
Ripley, TN
POSTED
30+ days ago
Benefits:
  • Competitive salary
  • Dental insurance
  • Health insurance
  • Paid time off
  • Training & development

Clinical Research Coordinator 



 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. 

 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! 

About the Company

M

Medovation Clinical Research LLC