Market Related
As a Project Administrator in our Clinical Trials team, you play a vital role in ensuring the smooth and timely preparation of laboratory kits, maintaining accurate stock levels, and supporting the team with essential administrative tasks.
As a Project Administrator in our Clinical Trials team, you play a vital role in ensuring the smooth and timely preparation of laboratory kits, maintaining accurate stock levels, and supporting the team with essential administrative tasks. This role is more than just coordination; it's about creating an environment where precision meets purpose.
Job Requirements
Role Requirements
To thrive in this role, you must have completed Grade 12. While not essential, a certification in GCP, GLP, or GCLP would be a valuable addition to your toolkit. These qualifications reflect your readiness to contribute to a learning-focused environment, where building future capabilities is part of our everyday journey. You bring at least two years of experience in administration, client services, or data capturing, ideally within a pathology or clinical trial setting. This experience equips you to navigate the complexities of clinical environments with confidence and care. Your background demonstrates your ability to engage meaningfully with both data and people, aligning with our strategy to attract and grow talent that delivers on our purpose
Skills Requirements
You are comfortable using technology to streamline tasks and enhance accuracy. Your communication skills allow you to connect clearly and professionally in English, both in writing and conversation. You approach numerical tasks with ease, and your attention to detail ensures that nothing slips through the cracks. Collaboration comes naturally to you; you build rapport effortlessly and contribute positively to team dynamics. Your understanding of good laboratory practices supports our shared commitment to quality and accountability. These skills reflect our belief in empowering leadership and fostering engagement through everyday excellence.
Role Impact
In this role, your impact is felt across the clinical trial journey. You monitor critical storage systems to ensure compliance, manage stock with care and foresight, and prepare laboratory kits that meet the highest standards. Your administrative support keeps the team moving forward, while your attention to documentation ensures data is stored and retrieved efficiently. You help maintain strong client relationships, reinforcing our reputation for reliability and professionalism. Every task you complete contributes to a culture of high performance, where people are empowered, engaged, and equipped to succeed. You are not just supporting trials, you are helping shape the future of clinical research.
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, especially those from underrepresented groups. We believe that diverse perspectives drive innovation and excellence in healthcare, and we are proud to create a space where everyone can thrive.
Hours of Work
40 hours per week
Work week
5 days
Location
Pretoria - Centurion
Closing Date
25 October 2025 at 21:00
now and take the next step in your career with Ampath, where purpose meets possibility.
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