Clinical Research Associate

Job Description

Join our team as a Clinical Research Associate to oversee and monitor clinical trial processes. We are looking for a motivated individual with the ability to ensure adherence to protocols and facilitate communication among stakeholders.

Responsibilities

• Lead site selection and feasibility assessments.
• Review and evaluate clinical data for reporting inconsistencies.
• Maintain current knowledge of clinical trial regulations.
• Facilitate communication between sponsors, sites, and other stakeholders.
• Identify issues and implement corrective actions as necessary.
• Develop study timelines and ensure milestones are met.
• Assist in audits and inspections from regulatory authorities.
• Prepare and provide training for new team members involved in clinical trials.

Requirements

Education

• Bachelor's degree in Health Sciences or related field
• Master's degree is advantageous

Experience

• 3+ years of experience in conducting clinical trials

Technical Skills

• Project Management
• Regulatory Knowledge

Soft Skills

• Interpersonal Skills
• Organizational Skills

Certifications

• Certified Clinical Research Associate (CCRA)
• Clinical Trials Operations Certificate

Languages

• English: Fluent

Advantageous

• Knowledge of biostatistics: Understanding statistical methods for analyzing clinical data.
• Experience in patient recruitment strategies: Implemented successful strategies to enhance patient participation in trials.

Benefits

• Comprehensive medical aid
• Annual leave and sick leave provisions
• Housing allowance
• Professional development opportunities

Company Culture

• Continuous Improvement: Our focus on continuous improvement drives our commitment to quality in research.
• Inclusivity: We celebrate diversity and promote an inclusive culture that empowers all team members.
• Employee Growth: We provide resources and opportunities for personal and professional development.