We are seeking a Clinical Research Coordinator to oversee and manage clinical trials. The ideal candidate will ensure compliance with study protocols and regulatory requirements while maintaining a high standard of participant care.
Responsibilities
Lead the execution of clinical trial protocols from initiation to completion.
Coordinate scheduling of study visits and participant assessments.
Ensure proper training and support for clinical staff.
Conduct regular audits to ensure compliance with study standards.
Resolve conflicts within the study team or with participants.
Assist in preparing for monitoring visits and audits.
Maintain participant confidentiality and data security.
Coordinate with laboratories for necessary testing and analysis.
Provide support during the data analysis phase.
Requirements
Education
Bachelor's degree in Nursing or a healthcare-related field
Advanced degree in Clinical Research or a related discipline is preferred
Experience
5+ years of experience in clinical research coordination or project management
Technical Skills
Regulatory Knowledge
Database Management
Soft Skills
Leadership
Critical Thinking
Certifications
Certified Clinical Research Associate (CCRA)
Certified Clinical Research Coordinator (CCRC)
Languages
English: Fluent
Xhosa: Conversational
Advantageous
Experience with biostatistics: Background in biostatistics to assist in data analysis.
Knowledge of project management methodologies: Understanding of agile or waterfall methodologies for project management.
Benefits
Comprehensive health benefits
Retirement savings plan with company contributions
Parental leave
Employee wellness programs
Company Culture
Continuous Improvement: We strive for continuous improvement in our research practices and methodologies.
Professional Growth: We provide opportunities for ongoing training and career development.
Community Engagement: We actively engage with the community to ensure that our research benefits all stakeholders.