Clinical Research Coordinator (Part/Full Time) - Impact & Growth

Medovation Clinical Research LLC; Ripley (TN); On-site; USD 40,000 - 65,000; Full time

Benefits offered by this job

Competitive salary

Dental insurance

Health insurance

Paid time off

Training & development

Job summary

Medovation Clinical Research LLC is seeking a Clinical Research Coordinator to join our on-site team supporting trials at physician practices in Tennessee. The role requires handling trial operations, data management, regulatory compliance, and blood sampling with a focus on accurate documentation.

The ideal candidate has at least one year of experience coordinating clinical research projects, knowledge of medical terminology, and phlebotomy skills. Travel between two sites is expected.

Qualifications

• 2+ years of experience coordinating clinical trials from initiation to completion.
• Proficiency in data entry and data management.
• Knowledge of medical terminology relevant to clinical research.
• Phlebotomy and blood sampling techniques are required.
• Patient recruitment experience is required.
• Travel between two sites: Jackson, TN and Ripley, TN (2 days at Jackson; 3 days at Ripley).

Responsibilities

• Manage day-to-day operations of clinical trials, ensuring adherence to protocols and timelines.
• Analyze data collected during trials and maintain accurate records for compliance.
• 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.

Skills

Phlebotomy

Data entry

Medical terminology

Patient recruitment

Organizational skills

Job description

Medovation Clinical Research LLC is seeking a Clinical Research Coordinator to join our on-site team supporting trials at physician practices in Tennessee. The role requires handling trial operations, data management, regulatory compliance, and blood sampling with a focus on accurate documentation.

The ideal candidate has at least one year of experience coordinating clinical research projects, knowledge of medical terminology, and phlebotomy skills. Travel between two sites is expected.