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Career & Industry Guide:

The Healthcare, Biotech, and Pharmaceutical industry is highly regulated, offering highly stable career pathways. Professionals work across research laboratories, manufacturing operations (under strict GMP guidelines), batch quality control, and clinical trial coordination. Ensuring product safety and chemical compliance is a high-responsibility role. Review verified industry openings, quality audit interview strategies, and lab safety certifications required to stand out in the healthcare and life-sciences domain.

Production Chemist - Remote

Placements24
📍 Rustenburg, Bojanala Platinum
October 06, 2026
About the Role Our client is seeking a dedicated and experienced Production Chemist to join their globally distributed technical team, working remotely. This role is crucial for ensuring the efficient and safe production of hydrocarbons by providing expert chemical analysis and process support. You will analyze fluid samples, troubleshoot production chemistry issues, and recommend chemical treatment programs to optimize performance and asset integrity. This is an excellent opportunity for a ski...
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Remote Medical Affairs Manager: Strategic Leader

Placements24
📍 Cape Town Region, Western Cape
October 06, 2026
Placements24 is seeking a highly experienced Medical Affairs Manager to lead the medical affairs function for a pharmaceutical portfolio. This fully remote leadership role requires strategic vision, scientific communication, and regulatory insight to shape the company’s medical strategy and engagement with stakeholders. You will oversee medical information, drive clinical program support, and maintain scientific integrity across communications, while guiding cross-functional teams in a remote J...
✔ Verified

Remote Medical Writer for Regulatory Submissions & Trials

Placements24
📍 South Africa
October 06, 2026
Placements24 is seeking a talented Medical Writer to join their globally distributed, remote-first medical affairs team. You will develop clear, scientifically sound documents for regulatory submissions, clinical trial reporting, and publications. Collaborate with medical, regulatory, and research teams to translate complex data into concise language, ensure regulatory compliance, and meet strict timelines in a fully remote environment. J-18808-Ljbffr
✔ Verified

Remote Medical Writer - Pharmaceutical

Placements24
📍 Stellenbosch, Cape Winelands
October 06, 2026
About the Role Our client is seeking a talented and experienced Remote Medical Writer to join their team, supporting communications efforts for projects based in Stellenbosch, Western Cape . This position is fully remote, enabling you to contribute to critical medical communication projects from any location in South Africa. You will be responsible for creating clear, accurate, and scientifically sound documents for regulatory, clinical, and marketing purposes, ensuring compliance with all rele...
✔ Verified

Senior Medical Aesthetician: Remote & Advanced Skincare

Placements24
📍 Soweto, West Johannesburg
October 06, 2026
Placements24 is seeking a highly skilled Senior Medical Aesthetician for a fully remote position serving clients nationwide from a home base near Soweto. You will apply expertise in medical-grade skincare, lasers, peels, and microneedling to guide remote consultations and treatment plans. You will educate clients and practitioners, support remote service offerings, and stay current with the latest advances in medical aesthetics to ensure high standards of care and outcomes. J-18808-Ljbffr
✔ Verified

Remote Senior Clinical Research Associate – Global Trials

Placements24
📍 Stellenbosch, Cape Winelands
October 06, 2026
Placements24 is seeking an accomplished Senior Clinical Research Associate to support critical trials remotely. The role focuses on monitoring sites, ensuring GCP compliance, and maintaining strong relationships with investigators and staff from a global, remote capacity. The ideal candidate has ≥5 years as a CRA, deep ICH-GCP knowledge, and the ability to travel for site visits when required. A life sciences degree is preferred, with a strong emphasis on quality and regulatory adherence. J-188...
✔ Verified

Remote Senior Clinical Trial Manager (German-Speaking)

The Global Talent Co.
📍 South Africa
October 06, 2026
ICON Clinical Research, a global sponsor-dedicated studies partner, seeks a Senior Clinical Trial Manager to lead country-level delivery from start-up through close-out. You will oversee feasibility, site activation, regulatory submissions, budgets, and cross-functional coordination to ensure high-quality study execution with inspection readiness. Ideal candidates will bring strong clinical operations leadership, extensive CRA/Study Management experience, and the ability to drive projects in a ...
✔ Verified

Remote Orthodontic Clinical Lead | Part-Time Mentor

Medical Resources Group Ltd
📍 South Africa
October 06, 2026
Medical Resources Group is recruiting on behalf of our client, a growing dental practice seeking an experienced Orthodontist to provide specialist support and clinical leadership across its practices. The position is designed for an orthodontist who enjoys clinical problem-solving, treatment planning and mentoring other dentists, with the flexibility of working primarily through remote case reviews rather than a full-time chairside role. J-18808-Ljbffr
✔ Verified

Remote Biostatistician — Clinical Trials & Data Insights

Placements24
📍 Randburg, West Johannesburg
October 06, 2026
Placements24 in South Africa is seeking a highly skilled Biostatistician to join its clinical research team, offering remote support to Randburg operations. You will design, analyze, and interpret clinical trial data, ensuring regulatory compliance and statistical rigor through SAS or R analyses. The ideal candidate holds a Master’s or PhD in Statistics or Biostatistics with at least four years’ experience in pharma or CRO settings, and strong communication skills. J-18808-Ljbffr
✔ Verified

Clinical Monitoring Analyst (Cluepoints) - Remote

IQVIA
📍 Bloemfontein, Mangaung
October 06, 2026
London, United Kingdom Budapest, Hungary Reading, Berkshire, United Kingdom Bloemfontein, South Africa Dublin, Ireland Centurion, South Africa Barcelona, Spain Sofia, Bulgaria Madrid, Spain Full time R1513972 This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor dedicated project where you will ...
✔ Verified
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