Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, your responsibilities will include overseeing clinical trial operations, liaising with investigators, and maintaining accurate study documentation, while ensuring adherence to protocols.

Responsibilities

• Lead the coordination of clinical trial activities and administrative processes.
• Work closely with Principal Investigators to implement study protocols.
• Ensure compliance with Good Clinical Practice (GCP) standards.
• Participate in the training of staff on clinical trial requirements.
• Monitor study progress and implement corrective actions as needed.
• Engage with community stakeholders for participant recruitment.
• Compile study reports and submit to regulatory authorities.
• Manage budgets and assist in financial reporting for clinical trials.

Requirements

Education

• Bachelor's degree in Medicine, Nursing, or Pharmacy
• Advanced degree (Master's or PhD) in relevant field is a plus

Experience

• 3+ years of relevant experience in clinical trials or research

Technical Skills

• Data Analysis Tools
• Clinical Research Regulations

Soft Skills

• Team Leadership
• Problem-Solving

Certifications

• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience in managing multi-site clinical trials: Experienced in coordinating trials across multiple research sites.
• Proficiency in statistical analysis software: Skilled in using software for statistical analysis in clinical research.