Clinical Research Associate

Job Description

Join our team as a Clinical Research Associate, where you'll engage in the planning and implementation of clinical trials. Your expertise will be crucial in maintaining the highest standards of patient safety and data quality throughout the study.

Responsibilities

• Oversee participant recruitment and retention strategies during clinical trials.
• Conduct monitoring visits and provide follow-up based on findings.
• Collaborate with cross-functional teams to ensure successful study delivery.
• Identify and mitigate risks throughout the clinical trial lifecycle.
• Support audit and inspection readiness by maintaining comprehensive study documentation.

Requirements

Education

• Bachelor's in Nursing or Medical Science
• Master's degree in Clinical Research preferred

Experience

• 3+ years in a clinical research environment

Technical Skills

• Project Management
• Ethical Compliance

Soft Skills

• Problem-Solving
• Teamwork

Certifications

• Clinical Research Associate Certification
• GCP Certification

Languages

• English: Fluent

Advantageous

• Experience with risk-based monitoring: Proven experience in implementing risk-based strategies in clinical trials.
• Familiarity with clinical trial management systems (CTMS): Hands-on experience with CTMS for trial tracking and reporting.

Benefits

• Health and wellness programs
• Competitive salary with performance bonuses
• Paid time off and holidays
• Employee assistance program

Company Culture

• Inclusivity: We value diversity and inclusion, creating a workplace where everyone feels welcome.
• Continuous Learning: We encourage ongoing exploration and learning to stay ahead in the medical research field.
• Professional Growth: We prioritize the professional development of our team members through mentorship and training.