Clinical research jobs South Africa

Snr Clinical Trial Assistant page is loaded Snr Clinical Trial Assistant Apply locations Centurion, South Africa time type Full time posted on Posted 2 Days Ago job requisition id R1414521 Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essentia...

Are you looking for an opportunity where you can utilize your medical knowledge to convey scientific data and interact with medical global thought leaders? Are you passionate about the world of clinical trials? Are you highly motivated by being able to make a difference in improving patients' lives? If so, we have an exciting Clinical Medical Manager opportunity for you. Apply today! The Position...

Main purpose of the job:To assist the Site Leader and Principal Investigators in coordinating all aspects of Clinical Trials, including clinic management, staffing, data collection, data storage, quality control, and project management, frequent communication with Study Investigators, Study Coordinators, and the Study teamLocation:Jose Pearson TB Hospital, Gqeberha (Port Elizabeth)Key performance...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master F...

CORE PURPOSE OF JOB Reporting to the Head of Department, the Clinical Co-Ordinator is required to: Coordinate the delivery of teaching and assessment of medical students on the clinicalhealthcare platform. Enhance the development of fit for purpose primary healthcare-oriented graduates. Function in close cooperation with the MBChB Coordinator in rolling out the clinical component of the MBChB pro...

Snr Clinical Trial Assistant page is loaded Snr Clinical Trial Assistant Apply locations Centurion, South Africa time type Full time posted on Posted 2 Days Ago job requisition id R1414521 Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essent...

Clinical Research and Development Specialist: HBM Ref: CRS/BM/LM Salary: Market related Location: Pretoria Large Managed Care organisation seeks to employ a suitably qualified and experienced Professional Nurse or Pharmacist to join the HBM department. Key responsibilities: Draft detailed, option-specific funding guidelines for HBM that are compliant with the principles of evidence -based medicin...

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $18 billion and approximately 55,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics and increase laboratory pro...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review cor...

Job Specification: Clinical Research and Development SpecialistLocation: GautengAbout Our Client: Our client is a leading medical scheme based in Pretoria, dedicated to providing comprehensive healthcare benefits to its members. They are committed to innovation, quality service, and the well-being of their clients.The position: Our client is seeking a Clinical Research and Development Specialist ...

Job Specification: Clinical Research and Development SpecialistLocation:GautengAbout Our Client:Our client is a leading medical scheme based in Pretoria, dedicated to providing comprehensive healthcare benefits to its members. They are committed to innovation, quality service, and the well-being of their clients.The position:Our client is seeking aClinical Research and Development Specialistto jo...

CAPRISA is an award-winning global research organisation located on the campus of the Nelson Mandela School of Medicine in Durban, South Africa and undertakes research in HIV, TB and Covid at four clinical research sites in KwaZulu-Natal. CAPRISA s goal is to undertake globally relevant and locally responsive research that contributes to understanding HIV Vaccines and Pathogenesis, Prevention and...

Principal Clinical Data Manager page is loaded Principal Clinical Data Manager Apply locations Western Springs time type Full time posted on Posted 2 Days Ago job requisition id JR 4213 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently a...

Main purpose of the job:To assist the Site Leader and Principal Investigators in coordinating all aspects of Clinical Trials, including clinic management, staffing, data collection, data storage, quality control, and project management, frequent communication with Study Investigators, Study Coordinators, and the Study teamLocation:Jose Pearson TB Hospital, Gqeberha (Port Elizabeth)Key performance...

CORE PURPOSE OF JOB To facilitate the acquisition of knowledge and skills by undergraduate pharmacy students for them to function effectively within the field of Pharmacy. To conduct and lead research, facilitate the acquisition of research knowledge and skills amongst undergraduate and postgraduate students. To contribute to community engagement and to be involved in the core functions of the Un...

Job Specification: Clinical Research and Development SpecialistLocation: GautengAbout Our Client: Our client is a leading medical scheme based in Pretoria, dedicated to providing comprehensive healthcare benefits to its members. They are committed to innovation, quality service, and the well-being of their clients.The position: Our client is seeking a Clinical Research and Development Specialist ...

Job Specification: Clinical Research and Development Specialist Location: Gauteng About Our Client: Our client is a leading medical scheme based in Pretoria, dedicated to providing comprehensive healthcare benefits to its members. They are committed to innovation, quality service, and the well-being of their clients. The position: Our client is seeking a Clinical Research and Development Speciali...

Main purpose of the job:To provide clinical expertise in support of clinical research activities, including recruiting and screening participants in research studies according to the study protocol and providing clinical insight and support to the local investigator and study managementLocation:Nelson Mandela Academic Hospital, Umtata Eastern CapeKey performance areas:Recruitment & RetentionScree...

Main purpose of the job:To provide clinical expertise in support of clinical research activities, including recruiting and screening participants in research studies according to the study protocol and providing clinical insight and support to the local investigator and study managementLocation:Nelson Mandela Academic Hospital, Umtata Eastern CapeKey performance areas:Recruitment & RetentionScree...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory r...

Introduction The Vaccines and Infectious Diseases Analytics (VIDA) Research Unit of the University of the Witwatersrand, formerly RMPRU (Respiratory and Meningeal Pathogens Research Unit) has for over 20 years conducted numerous studies to assess the burden of and prevent vaccine-preventable diseases (VPD). Current studies and projects include infant rotavirus and BCG trials. Description Main pur...