ich

Placements24 is seeking a skilled Remote Medical Writer to produce high-quality clinical and regulatory documents for a global audience. You will translate complex data into clear, accurate content, supporting drug development and regulatory submissions across therapeutic areas. The role is fully remote, requiring 3+ years of medical writing experience, a...

Placements24 in Centurion seeks a Lead Analytical Chemist to direct crucial analytical activities at a state-of-the-art facility. You will oversee development, validation, and application of analytical methods to ensure the quality of research materials and products. You will manage and mentor a team of chemists, ensure GLP/ICH compliance, and collaborate...

Placements24 seeks a Medical Writer in Bloemfontein to produce clear, accurate regulatory and scientific documentation for pharmaceutical products. You will craft CSRs, manuscripts, and patient information leaflets while ensuring compliance with ICH, FDA, EMA guidelines. Collaborating with scientists and regulatory professionals, you will translate complex...

Placements24 in South Africa seeks a Senior Clinical Research Associate to oversee and manage clinical trials in the Klerksdorp area. You will monitor sites, ensure data integrity, and support investigators to uphold protocol and regulatory standards.The role requires a life sciences degree, at least 5 years as a CRA, solid ICH-GCP knowledge, and ability to...

Placements24 is seeking an Analytical Development Chemist for our client in Nelspruit to develop, validate and transfer analytical methods for drug substances and products, supporting development and commercialization while ensuring quality and compliance. The role requires 3+ years in pharmaceutical analytical method development, expertise in HPLC/GC and...

Our client is seeking a skilled Analytical Development Chemist to join their expanding laboratory services in Nelspruit. This role focuses on developing, validating, and transferring analytical methods for raw materials, intermediates, and finished pharmaceutical products. You will utilize your expertise in various analytical techniques to ensure the...

A leading recruitment agency seeks a Clinical Medical & Regulatory Director to lead clinical research programs and ensure regulatory compliance. This role involves strategic leadership, managing relationships with regulatory authorities, and overseeing clinical trials. The ideal candidate will have a strong understanding of GCP and ICH guidelines, proven...

Placements24 seeks a meticulous and experienced Clinical Research Associate (CRA) to join the clinical operations team in Cape Town. You will oversee site monitoring, data verification, and ensure adherence to protocols and regulatory standards. The ideal candidate has a life sciences degree, CRA experience, and strong knowledge of ICH-GCP. Excellent...

Placements24 is seeking an experienced Clinical Trial Manager to oversee end-to-end trial execution in Randburg. You will lead cross-functional teams, manage timelines, budgets and vendors, ensuring compliance with protocols, GCP/ICH, and regulatory requirements. The role demands strong leadership, clear communication, and proactive problem-solving to...

Smollan is seeking a Regulatory and Start Up Specialist 2 for a hybrid, Gauteng-based role. You will manage country-level site activation activities, ensure SOP/compliance with GCP/ICH guidelines, and act as SPOC for sites and project teams. Responsibilities include preparing regulatory documents, maintaining systems, and supporting proposal development...

MMS is a data-focused clinical research organization seeking a Senior Data Team Lead for a home-based role across South Africa. The candidate will manage the full data lifecycle from study setup to close-out, serving as the primary client and internal DM contact, with strong knowledge of GCP/ICH and FDA requirements. Role requires extensive data management...

IQVIA is seeking a Global Study Manager to support delivery of clinical studies within BioPharmaceuticals Clinical Operations, spanning CSP development through CSR, study setup, maintenance, and archiving.The role requires leadership, cross-functional collaboration, and strong knowledge of ICH/GCP guidelines to ensure on-time, on-budget study delivery with...

Placements24 is seeking a skilled Pharmaceutical Clinical Research Associate (CRA) to join a globally integrated, fully remote team with operations extending to the Benoni area. This role monitors study sites, ensures data integrity, and protects patient safety throughout the trial lifecycle.The ideal candidate has a Bachelor's degree in life sciences and at...

Placements24 is seeking a detail-oriented Regulatory Affairs Specialist in Polokwane to manage global submission activities for pharmaceutical products. You will prepare, review, and submit regulatory dossiers, liaise with health authorities, and monitor lifecycle management across international markets.The role requires a Bachelor's degree and at least 4...

International AIDS Vaccine Initiative, Inc. is seeking a Clinical Trial Manager / Senior Clinical Trial Manager to lead day-to-day operational activities for clinical trials under ICH/GCP and regulatory guidelines. The role spans early and late-phase trials, with mentoring responsibility for operations staff and process improvements. The position requires...

Placements24 is seeking an experienced Remote Pharmaceutical Clinical Research Associate (CRA) to oversee multicenter trials across therapeutic areas. The role is fully remote, offering flexibility to work from anywhere while ensuring trial data integrity and compliance with GCP, FDA/ICH regulations. You will conduct remote and on-site monitoring as...

Placements24 in Mbombela (Nelspruit) seeks a skilled Medical Writer specializing in clinical documentation to join their hybrid team. You will prepare high-quality regulatory documents for clinical trials, collaborating with regulatory affairs, R&D and operations. The role combines remote work with on-site collaboration in a scenic location, offering...

Placements24 in Mossel Bay is seeking a Senior Pharmaceutical Chemist to lead the Analytical Development team. You will develop, validate and implement robust analytical methods for drugs and raw materials, ensuring data accuracy for regulatory submissions. The ideal candidate has 7+ years in method development/validation, strong HPLC and MS experience, and...

Placements24 is seeking an experienced Senior Analytical Scientist to join its pharmaceutical development team in Mossel Bay. The role centers on developing, validating, and implementing analytical methods for characterizing and QC of drug substances and products, leveraging instruments like HPLC, GC, UV-Vis, and dissolution testing. You will work in a...

Cytel is seeking a Principal Statistical Programmer to work within a sponsor-dedicated team in Cape Town. You will manage SDTM, ADaM, define.xml artifacts, generate complex listings and graphs in SAS and R, and oversee CRO deliverables for multiple studies.You will contribute to regulatory submissions, DSURs, and exploratory analyses while ensuring...