Part-Time Clinical Research Coordinator: Impactful Trials

Medovation Clinical Research LLC; Jackson (TN); On-site; USD 34,000 - 48,000; Part 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 Part Time Clinical Research Coordinator to join an integrated clinical research organization focused on expanding access to trials. The role is on-site at the physician’s practice and emphasizes meticulous data management and regulatory compliance.

The ideal candidate has at least one year coordinating clinical research from initiation to completion, with phlebotomy skills.

Qualifications

• Minimum 1 year of experience as a Clinical Research Coordinator (CRC) required.
• 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.

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

CRC experience

Data entry

Medical terminology

Phlebotomy

Patient recruitment

Organization

Job description

Medovation Clinical Research LLC is seeking a Part Time Clinical Research Coordinator to join an integrated clinical research organization focused on expanding access to trials. The role is on-site at the physician’s practice and emphasizes meticulous data management and regulatory compliance.

The ideal candidate has at least one year coordinating clinical research from initiation to completion, with phlebotomy skills.