Clinical Research Associate

Job Description

We are seeking a motivated Clinical Research Associate to lead clinical trials that enhance our understanding of medical treatments. Your expertise will guide the study design and implementation, ensuring adherence to ethical standards and protocols.

Responsibilities

• Plan, implement, and oversee clinical research protocols.
• Review and analyze data to ensure scientific integrity.
• Communicate effectively with study participants, addressing any concerns.
• Ensure compliance with ethical standards throughout the research process.
• Maintain meticulous records of trial activities and results.
• Support the preparation for audits and inspections by regulatory authorities.

Requirements

Education

• Bachelor's degree in Life Sciences or related field
• Master's degree is an advantage

Experience

• 2-4 years of experience in clinical research or related field

Technical Skills

• Clinical Trial Management
• Regulatory Compliance

Soft Skills

• Attention to Detail
• Communication Skills

Certifications

• Certified Clinical Research Associate (CCRA)
• Good Clinical Practice (GCP) certification

Languages

• English: Fluent

Advantageous

• Experience with EDC systems: Familiarity with electronic data capture systems used in clinical trials.
• Knowledge of biostatistics: Understanding of statistical methods applied in clinical research.

Benefits

• Medical aid coverage
• Flexible work hours
• Professional development opportunities
• Annual leave and sick leave

Company Culture

• Teamwork: We promote a culture of collaboration and unity among our staff.
• Innovation: Encouraging innovative ideas and solutions in our research.
• Integrity: We uphold the highest ethical standards in our research activities.