Clinical Research Assistant 260209

Medix Staffing Solutions, Inc.; Marietta (GA); On-site; USD 60,000 - 75,000; Full time

Job summary

Medix Staffing Solutions, Inc. is seeking a Clinical Research Coordinator to oversee the operation of clinical trials, recruit and screen study subjects, and ensure high-quality data collection in compliance with FDA guidelines.

The role emphasizes adherence to GCP, protocol compliance, and ongoing coordination with sponsors and study participants to maintain data integrity and SOP adherence.

Responsibilities

• Oversee the efficient operation of a clinical trial
• Recruit and screen study subjects to participate in trials
• Collect and report accurate data obtained from research to support data integrity
• Maintain detailed documentation and records of clinical studies in compliance with FDA guidelines
• Monitor research participants to provide adherence to study protocol
• Provide accountability for clinical study supplies and Investigational Product
• Provide for the routine calibration and maintenance of equipment utilized in clinical trials
• Adherence to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards
• Provide leadership for clinical research staff
• Maintain relationships with study subjects and sponsor delegates
• Perform other related duties as assigned by the Principal Investigator
• Maintain compliance with all research Standard Operating Procedures (SOPs)

Job description

• Oversee the efficient operation a clinical trial
• Recruit and screen study subjects to participate in trials
• Collect and report accurate data obtained from research to support data integrity
• Maintain detailed documentation and records of clinical studies in compliance with FDA guidelines
• Monitor research participants to provide adherence to study protocol
• Provide accountability for clinical study supplies and Investigational Product.
• Provide for the routine calibration and maintenance of equipment utilized in clinical trials
• Adherence to Good Clinical Practice (GCP) guidelines including regulatory and ethical standards
• Provide leadership for clinical research staff
• Maintain relationships with study subjects and sponsor delegates
• Perform other related duties as assigned by the Principal Investigator
• Maintain compliance with all research Standard Operating Procedures (SOPs)