Clinical Research Associate

Job Description

Join our dedicated research team as a Clinical Research Associate in Durban, where you'll play a pivotal role in managing clinical trials and ensuring the collection of high-quality data for our studies.

Responsibilities

• Conduct feasibility assessments for upcoming clinical studies.
• Collaborate with the regulatory team on submissions and approvals.
• Facilitate study meetings and maintain documentation.
• Track and manage study budgets and timelines.
• Prepare and submit required documentation to ethics committees.
• Ensure adherence to Good Clinical Practice (GCP) standards.

Requirements

Education

• Bachelor's degree in a relevant field
• Master's degree in Clinical Research or related field is preferred

Experience

• 3+ years of experience in clinical research monitoring

Technical Skills

• Regulatory Compliance
• Clinical Data Management

Soft Skills

• Leadership
• Attention to Detail

Certifications

• ICH-GCP Certified
• Clinical Research Certification from ACRP

Languages

• English: Fluent

Advantageous

• Experience with patient recruitment strategies: Understanding of effective techniques to enhance patient recruitment in clinical studies.
• Prior experience in phase I trials: Involvement in phase I clinical trials and related research.

Benefits

• Comprehensive health and wellness benefits
• Performance bonuses based on project success
• Flexible working hours
• Career advancement opportunities

Company Culture

• Diversity and Inclusion: We embrace diversity and promote an inclusive workplace where all team members can thrive.
• Continuous Growth: We believe in continuous professional development and offer training programs for our staff.
• Client-centric Focus: Our research initiatives are centered around the needs of clients and patients.