We are looking for a detail-oriented Clinical Research Associate to manage and coordinate clinical trials in Johannesburg. The ideal candidate will have a background in medical research and a passion for improving healthcare outcomes.
Responsibilities
Lead the management of multiple clinical trials from initiation to completion.
Monitor participant recruitment and retention rates to meet trial timelines.
Review and approve site monitoring reports and documentation.
Facilitate communication with investigators and site staff.
Ensure that data management and safety reporting are timely and accurate.
Participate in team meetings to update stakeholders on trial progress.
Assist in the preparation of trial budgets and timelines.
Support the clinical project manager with regulatory submissions and compliance.
Maintain an organized trial master file and related documents.
Requirements
Education
Master's degree in Life Sciences or related field is preferred
Experience
5+ years of experience in clinical research
Technical Skills
Project Management
Statistical Analysis Software
Soft Skills
Team Leadership
Problem-Solving
Certifications
Clinical Research Associate (CRA)
Certified Clinical Research Associate (CCRA)
Languages
English: Fluent
Advantageous
Previous experience with site management: Experience in managing clinical sites and interacting with site staff.
Familiarity with medical writing: Ability to contribute to the preparation of study protocols and reports.
Benefits
Attractive salary package and yearly bonus
Health insurance for you and your family
Work-life balance initiatives
Ongoing training and certification options
Company Culture
Continuous Learning: We encourage ongoing education and training to keep our team at the forefront of research developments.
Diversity and Inclusion: Diversity is integral to our success, and we promote an inclusive workplace for all.
Community Engagement: We actively engage with the community to improve public health and wellness.