Clinical Research Associate

Job Description

As a Clinical Research Associate, you will support the execution of clinical research projects, ensuring that trials are conducted ethically and efficiently. You will collaborate with diverse teams and contribute to the advancement of healthcare solutions.

Responsibilities

• Conduct assessments and follow-ups with trial participants.
• Record adverse events and ensure reporting complies with safety regulations.
• Support the clinical operations team in all administrative tasks related to trials.
• Maintain excellent communication with all stakeholders throughout the clinical process.
• Assist in generating study reports and contribute to publications.

Requirements

Education

• Bachelor's degree in Health Sciences or relevant studies
• Master’s degree in Clinical Research or related field preferred

Experience

• 3+ years of experience in clinical research.

Technical Skills

• Regulatory Compliance
• Clinical Data Management Systems

Soft Skills

• Leadership
• Problem-solving

Certifications

• Certified Clinical Research Associate (CCRA)
• Regulatory Affairs Certification (RAC)

Languages

• English: Fluent

Advantageous

• Knowledge of biostatistics: Ability to analyze clinical data using statistical software.
• Previous experience with FDA submissions: Understanding of regulatory documents and processes for submissions.

Benefits

• Comprehensive medical aid with access to specialists.
• Retirement fund contributions.
• Generous annual leave policy.
• Professional development opportunities and training reimbursement.

Company Culture

• Diversity: We embrace diversity and inclusivity in our workforce.
• Continuous Improvement: We foster an environment where continuous learning and development is encouraged.
• Commitment to Quality: Our dedication to quality ensures the reliability of our research results.