Clinical Research Associate

Job Description

We are seeking a dedicated Clinical Research Associate to facilitate clinical research activities. You will collaborate with various teams to implement study protocols, monitor patient data, and support the overall research objectives campaign.

Responsibilities

• Coordinate all operational aspects of clinical trials.
• Ensure compliance with Good Clinical Practice (GCP) guidelines.
• Assist in the selection and initiation of study sites.
• Prepare and manage study initiation, monitoring, and closure reports.
• Collaborate with data management teams to ensure data accuracy.
• Address site queries and resolve any issues related to the trial process.
• Facilitate regular updates and feedback sessions with study stakeholders.

Requirements

Education

• Bachelor's degree in Health Sciences or related field
• Relevant certifications are advantageous

Experience

• 3-5 years in clinical research coordination or monitoring

Technical Skills

• Project Management
• Statistical Analysis Software (SAS)

Soft Skills

• Teamwork
• Flexibility

Languages

• English: Fluent
• Afrikaans: Conversational

Advantageous

• Experience in multi-site clinical trials: Previous experience managing clinical trials across multiple study sites.
• Proficiency in regulatory submissions: Strong understanding of the submission processes for clinical trials.

Benefits

• Health insurance, including dental and vision
• Retirement pension plan with employer contributions
• Paid time off and holidays
• Continuing education allowances for courses and workshops

Company Culture

• Diversity: We are committed to a diverse and inclusive workplace where everyone feels welcome.
• Team Spirit: We foster a supportive environment encouraging teamwork and respect.