Project Manager (Clinical Trials) | Centurion Gauteng

Ampath is actively recruiting for a Project Manager (Clinical Trials) | Centurion position in Gauteng. This is an excellent opportunity for professionals in the Medical / Healthcare sector looking to advance their careers.

• Experience Level: 3 years • Educational Background: Others or equivalent • Industry Focus: Medical / Healthcare • Location Preference: in Gauteng

Healthcare professionals including Project Manager (Clinical Trials) | Centurion are essential service providers. This role contributes directly to community health and wellbeing.

This role in Medical / Healthcare offers valuable career progression opportunities aligned with your experience level and professional aspirations.

When applying for this Project Manager (Clinical Trials) | Centurion position, ensure your CV highlights: • Relevant experience matching the 3 years requirement • Educational qualifications in line with Others • Specific achievements in the Medical / Healthcare field • Any certifications or specialized training

The Medical / Healthcare sector in South Africa continues to show strong demand for skilled professionals. This position represents a valuable opportunity in the current job market.

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As a Project Manager (Clinical Trials), you will play a pivotal role in ensuring the successful set-up and coordination of clinical trials from initiation through to implementation. This role is focused on translating trial requirements into well-planned, compliant, and operationally ready studies, ensuring that all processes, systems, and requirements are thoroughly tested and in place before a trial begins.

Working closely with a variety of stakeholders, you will help create an environment where collaboration, accountability, and excellence thrive. Your contribution will support high-quality outcomes while fostering strong partnerships, continuous learning, and a culture that encourages people to deliver their best work. This is an exciting opportunity for someone who is passionate about clinical research, enjoys working in a dynamic environment, and takes pride in making a meaningful impact on healthcare services and patient outcomes.

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.