Clinical Research Coordinator

Job Description

As a Clinical Research Coordinator, you will be responsible for managing clinical trial activities in Pretoria. This includes recruiting participants, monitoring trial progress, and ensuring adherence to ethical guidelines and regulations. Your contributions will be vital in advancing our medical research goals.

Responsibilities

• Plan and coordinate logistics for clinical trial initiation and closure.
• Ensure participant safety and well-being throughout the trial.
• Facilitate communication between the research team and external stakeholders.
• Implement quality assurance measures to maintain data integrity.
• Prepare study budgets and manage financial aspects related to trials.

Requirements

Education

• Bachelor's degree in Nursing or Health Sciences
• Advanced degree in related field is an advantage

Experience

• 3+ years of experience in a clinical research setting

Technical Skills

• Regulatory Knowledge
• Patient Recruitment Strategies

Soft Skills

• Team Leadership
• Problem-Solving

Certifications

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

Languages

• English: Fluent

Advantageous

• Knowledge of medical terminology: In-depth understanding of medical and pharmaceutical terminology.
• Previous experience with multi-site trials: Experience managing clinical trials across multiple locations.

Benefits

• Comprehensive health benefits including dental and vision
• Wellness programs and fitness memberships
• Flexible working hours and remote work options
• Generous annual leave and sick leave policies

Company Culture

• Professional Development: We support ongoing training and professional growth for all employees.
• Employee Wellbeing: Employee wellbeing is paramount, and we offer various resources to support mental and physical health.
• Community Engagement: We value community involvement and encourage staff to participate in outreach initiatives.