Clinical Research Coordinator

Job Description

We are looking for a dedicated Clinical Research Coordinator to oversee clinical research projects. This position requires a comprehensive understanding of clinical trial management, regulatory compliance, and participant engagement. You will work alongside various departments to facilitate project timelines and ensure that high-quality data is collected and managed effectively.

Responsibilities

• Design and implement study-specific protocols and recruitment strategies.
• Ensure compliance with relevant regulations during clinical study execution.
• Manage daily operations of clinical trials, including documenting findings.
• Act as the primary liaison between study sponsors and investigative sites.
• Review and analyze study data for accuracy and completeness.
• Prepare reports and presentations for review by stakeholders.
• Facilitate the ethical review process and communication with IRBs.
• Resolve queries related to regulatory compliance promptly.

Requirements

Education

• Bachelor's degree in a relevant field

Experience

• Experience in managing multi-center clinical trials is a plus.

Technical Skills

• Statistical analysis software (e.g., SAS, SPSS)

Soft Skills

• Problem-solving

Languages

• English: Fluent

Advantageous

• Knowledge of FDA regulations: Understanding FDA regulations and their implications in clinical trials.

Benefits

• Comprehensive health coverage
• 401(k) retirement plan with matching contributions
• Flexible scheduling for work-life balance
• Access to professional development courses

Company Culture

• Innovation: We value innovation in our approach to clinical research, encouraging fresh ideas and creative solutions.
• Supportive Environment: Our team is dedicated to providing a supportive work environment, aiding one another in our shared goals.
• Work-Life Balance: We recognize the importance of work-life balance and strive to create flexible working conditions for our staff.