Project Manager (Clinical Trials) | Centurion

Role Qualification Requirements To be successful in this role, you will have completed Grade 12 as a minimum requirement. Additional qualifications that will strengthen your application include certification in Good Clinical Practice (GCP), Good Laboratory Practice (GLP), or Good Clinical Laboratory Practice (GCLP), as these demonstrate a strong understanding of recognised industry standards and regulatory expectations. A Project Management certification will be advantageous, particularly for candidates who enjoy coordinating complex activities and driving projects to successful completion. A qualification as a Medical Technician or Medical Technologist will also be beneficial, providing a valuable foundation for understanding the clinical and laboratory environments in which trials operate. Role Experience Requirements You will bring at least three years of experience within a clinical trials environment, coupled with exposure to project management activities within clinical research. This experience will have equipped you with a solid understanding of trial set-up requirements, study coordination, stakeholder engagement, and the importance of maintaining compliance throughout the clinical trial lifecycle. The ideal candidate will be comfortable working across multiple priorities while maintaining a strong focus on quality, accuracy, and collaboration. Experience in coordinating activities with multidisciplinary teams and supporting successful project delivery will enable you to contribute effectively from the outset. An appreciation for continuous improvement and a willingness to share knowledge with others will be highly valued, supporting a culture where learning and capability development are encouraged. Role Skills Requirements This role requires an individual who combines technical knowledge with strong interpersonal and organisational capabilities. You will have confidence in using computer technology and digital tools to manage information effectively, while demonstrating excellent communication skills with the ability to read, write, and speak fluent English. You will possess sound numerical reasoning skills and a meticulous approach to detail, ensuring accuracy and consistency across all aspects of your work. Strong analytical thinking will allow you to evaluate complex situations, identify underlying issues, and contribute practical solutions that support successful project outcomes. Building meaningful working relationships will be central to your success. You will be comfortable engaging with a diverse range of stakeholders, including clients, colleagues, and cross-functional teams, fostering an environment built on trust, professionalism, and collaboration. A sound understanding of Good Clinical Practice (GCP), regulatory requirements, and good laboratory practices is essential, alongside the ability to apply this knowledge effectively within a clinical research setting. You will also bring project management expertise, enabling you to coordinate activities, monitor progress, and ensure that trial requirements are met in a structured and compliant manner. Familiarity with project management tools and methodologies will support your ability to plan, organise, and guide activities while contributing to a culture of accountability, continuous improvement, and high performance. Role Impact As a Project Manager (Clinical Trials), your work will directly contribute to the effective delivery of clinical trials and the quality of services provided to clients and stakeholders. You will lead the set-up of new trials, ensuring that study requirements are accurately translated into operational processes that meet applicable standards and regulatory expectations. You will coordinate trial-related administration to ensure information is recorded, distributed, and maintained appropriately, while partnering with cross-functional teams to support alignment and readiness throughout the trial journey. Your oversight of clinical trial storage systems will contribute to maintaining compliance and protecting the integrity of trial materials. Beyond operational responsibilities, you will play an important role in strengthening relationships with clients and colleagues, promoting a positive and professional experience for all stakeholders. Through your collaborative approach, commitment to learning, and dedication to excellence, you will help create an environment where people are empowered to succeed, innovation is encouraged, and quality remains at the heart of everything we do. Employment Equity and Diversity At Ampath, we are committed to building a diverse and inclusive workforce that reflects the communities we serve. In line with our Employment Equity goals, we actively encourage applications from individuals across all backgrounds, particularly those from underrepresented groups. We believe that diverse perspectives strengthen innovation, collaboration, and excellence in healthcare, and we are proud to create an environment where every individual feels valued, respected, and empowered to thrive. Hours of Work 40 hours per week Work week 5 days Location Centurion Closing Date 19 August 2026 at 21:00 Apply now and take the next step in your career with Ampath, where purpose meets possibility. 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