Clinical Research Associate

Job Description

Join us as a Clinical Research Associate where you'll manage clinical trials, ensuring compliance with regulatory requirements and protocols. This role crucially contributes to the successful execution of research projects that impact global health.

Responsibilities

• Coordinate and manage clinical trials according to Good Clinical Practice (GCP) guidelines.
• Monitor patient recruitment and retention activities to meet protocol milestones.
• Ensure the integrity and quality of research data through regular audits.
• Prepare and review study documentation including protocols, informed consent forms, and reports.
• Maintain communication with study sponsors and regulatory authorities to ensure compliance.
• Train and support site staff on clinical trial protocol and procedures.

Requirements

Education

• Bachelor's degree in Health Sciences or similar
• Master's degree in Public Health or related field is preferred

Experience

• 3+ years of experience in clinical trials or study management

Technical Skills

• Project Coordination
• Regulatory Compliance

Soft Skills

• Communication
• Team Leadership

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Experience with EDC systems: Familiarity with Electronic Data Capture (EDC) systems in clinical trials.
• Knowledge of ICH guidelines: Understanding of International Conference on Harmonisation (ICH) guidelines for clinical trials.

Benefits

• Comprehensive health cover including dental and vision.
• Retirement savings plan with employer contributions.
• Professional development opportunities and training.
• Flexible working hours.

Company Culture

• Integrity: We uphold the highest ethical standards in our research practices.
• Innovation: We encourage creativity and innovation in our team members.
• Collaboration: Our teamworks collaboratively, valuing each member's contribution.