Clinical Research Coordinator — On-Site Trials & Phlebotomy

Medovation Clinical Research LLC; Auburn (AL); On-site; USD 30,000 - 39,000; 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 at a physician's practice. You will manage trials, ensure regulatory compliance, and support data management.

The ideal candidate has at least two years of coordinating clinical research, phlebotomy skills, and a strong background in medical terminology. We offer a collaborative, mission-driven environment with opportunities for growth and development.

Qualifications

• Minimum 2 years coordinating clinical research projects.
• Phlebotomy skills required.
• Experience in data management and regulatory compliance.
• Knowledge of medical terminology relevant to clinical trials.
• On-site role in physician practice.

Responsibilities

• Manage day-to-day operations of clinical trials per protocol.
• Analyze data and maintain compliant records.
• Oversee blood sampling and proper handling.
• Provide training on trial protocols.
• Collaborate with healthcare professionals to ensure participant safety.
• Utilize software for data capture and reporting.
• Maintain clear communication with team and stakeholders.
• Ensure adherence to ethical standards and regulatory requirements.

Job description

Medovation Clinical Research LLC is seeking a Clinical Research Coordinator to join our on-site team at a physician's practice. You will manage trials, ensure regulatory compliance, and support data management.

The ideal candidate has at least two years of coordinating clinical research, phlebotomy skills, and a strong background in medical terminology. We offer a collaborative, mission-driven environment with opportunities for growth and development.