Clinical Research Coordinator — Drive Onsite Trials & Growth

Medovation Clinical Research LLC; Ripley (TN); On-site; USD 55,000 - 70,000; Full time

Benefits offered by this job

Competitive salary

Dental insurance

Health insurance

Paid time off

Training & development

Job summary

Medovation Clinical Research is seeking a Clinical Research Coordinator (Full Time) to manage and oversee clinical trials at a physician’s practice. The role requires phlebotomy skills and a strong background in medical terminology, data management, and trials coordination, with at least one year ofCRC experience.

On-site work in Ripley, TN, with a collaborative team and opportunities for growth as the company expands its access to clinical research for diverse patient communities.

Qualifications

• Minimum 1 year of experience as a Clinical Research Coordinator (CRC) required.
• Phlebotomy skills required.
• Knowledge of medical terminology relevant to clinical research.
• Proficiency in data entry.
• Patient recruitment experience required.

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.

Skills

Clinical experience

CRC experience

Data entry

Medical terminology

Phlebotomy

Blood sampling

Patient recruitment

Organizational skills

Travel to Ripley TN

Tools

Data capture software

Job description

Medovation Clinical Research is seeking a Clinical Research Coordinator (Full Time) to manage and oversee clinical trials at a physician’s practice. The role requires phlebotomy skills and a strong background in medical terminology, data management, and trials coordination, with at least one year ofCRC experience.

On-site work in Ripley, TN, with a collaborative team and opportunities for growth as the company expands its access to clinical research for diverse patient communities.