Clinical Research Associate

Job Description

As a Clinical Research Associate, you will contribute to our cutting-edge research projects in Port Elizabeth. Your responsibilities will include the management of clinical trial sites, ensuring clinical data integrity, and preparing regulatory submissions, allowing our team to advance innovative medical solutions.

Responsibilities

• Support the setup and management of clinical trials.
• Monitor patient recruitment and retention strategies.
• Evaluate the performance of clinical trial sites and ensure adherence to timelines.
• Conduct regular audits of data quality and compliance
• Facilitate communications between sponsors and regulatory bodies.
• Analyze and report data findings to stakeholders.
• Develop procedural manuals and training materials for site staff.
• Assist in regulatory submissions and responses.

Requirements

Education

• Bachelor's degree in Life Sciences or related field

Experience

• 2+ years of experience in clinical research or related field

Technical Skills

• Clinical Trial Management
• Data Analysis
• Regulatory Knowledge

Soft Skills

• Communication Skills
• Problem-solving

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Experience with Statistical Software: Proficient in using statistical software such as SPSS or SAS.
• Knowledge of Good Clinical Practice (GCP): Familiarity with guidelines for research involving human subjects.

Benefits

• Competitive salary package
• Health and wellness benefits
• Opportunity for professional development
• Flexible working hours

Company Culture

• Teamwork: We promote a culture of collaboration where team members support each other.
• Innovation: A culture that encourages creative thinking and innovation in research methodologies.
• Integrity: We value transparency and ethical practices in all our operations.