Clinical Research Associate

Job Description

We are looking for a detail-oriented Clinical Research Associate to assist with numerous clinical studies. You will coordinate between sponsors, CROs, and sites to ensure smooth study progression and strict adherence to timelines.

Responsibilities

• Develop and implement monitoring plans for studies.
• Assess site performance and adherence to Good Clinical Practice (GCP).
• Conduct regular audits to maintain data integrity.
• Document all findings and actions in the trial database.
• Facilitate communication and collaboration among all stakeholders.
• Assist in the development of training materials for study staff.

Requirements

Education

• Master's degree in Clinical Research or related field

Experience

• 4+ years of experience in the clinical research field with a focus on monitoring.

Technical Skills

• Regulatory Compliance
• Protocol Development

Soft Skills

• Leadership
• Problem-solving

Certifications

• Certified Clinical Research Associate (CCRA)
• Certified Clinical Research Coordinator (CCRC)

Languages

• English: Fluent

Advantageous

• Proficiency in project management software: Experience in using project management tools to schedule activities.
• Fluency in Afrikaans or Zulu: Ability to communicate in local languages can be an advantage.

Benefits

• Health and dental benefits
• Generous leave policies
• Continuing education support
• Employee discounts on health-related programs

Company Culture

• Community Engagement: We believe in giving back to the community we serve.
• Continuous Improvement: Our culture is rooted in learning and development for all employees.
• Diversity and Inclusion: We embrace diversity and are committed to fostering an inclusive workplace.