SD Recruitment is looking for a Senior Research Pharmacist tfor a 2 month contract (possibility of extension) based in Crossroads.The main purpose of this position is to manage the pharmacy according to South African Pharmacy Council (SAPC), Medicines Control Council (MCC), National Institutes of Health (NIH), Good Clinical and Good Pharmacy Practice Guidelines (GCP and GPP).The Pharmacy Manager ...
Right to Care is at the vanguard in supporting and delivering prevention, care, and treatment services for HIV and associated diseases. We work with government and communities to find pioneering solutions to build and strengthening public healthcare. We embrace a strong entrepreneurial culture and focused on innovation and the use of technology to enhance services, address skills shortages, and d...
Watchmaker Genomics is a global life science company with an R&D and Production facility in Cape Town, South Africa and head offices in Boulder, Colorado. Our team is passionate about innovation and we value collaboration, creativity and scientific rigor. We believe that the intersection of biology, engineering and computer science presents exciting opportunities for developing novel technologies...
Company Description NielsenIQ works with clients to provide insights, thought leadership to drive their business and grow their portfolios. Our work helps our clients set growth strategies and determines what products you ultimately see on the shelf. Our team members are experts across various categories and are viewed as trusted partners by our clients. Company Description NielsenIQ works with c...
Company DescriptionNielsenIQ works with clients to provide insights, thought leadership to drive their business and grow their portfolios. Our work helps our clients set growth strategies and determines what products you ultimately see on the shelf. Our team members are experts across various categories and are viewed as trusted partners by our clients. Company DescriptionNielsenIQ works with cli...
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations QA Associate , and is responsible for creating, developing, monitoring and managing quality systems that support ongoing Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this position works on complex problems requiring data analysis and the...
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations QA Associate , and is responsible for creating, developing, monitoring and managing quality systems that support ongoing Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this position works on complex problems requiring data analysis and the...
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...
Main purpose of the job: The primary purpose is to recruit and ensure the retention of study participants in line with the study protocol To perform administrative duties and assist the study team with ad hoc administrative duties Location: VIDA - Mafikeng Provincial Hospital Northwest Province Key performance areas: Recruitment of Participants Assist the Medical Officer in recruiting participant...
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: The primary purpose is to recruit and ensure the retention of study participants in line with the study protocol To perform administrative duties and assist the study team with ad hoc administrative duties Location: VIDA - Mafikeng Provincial Hospital Northwest Province Key performance areas: Recruitment of Participants Assist the Medical Officer in recruiting participant...
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...
The person will be responsible for the following: * Provide clinical oversight, timely medical advice and ensure implementation of all medical matters relating to blood donors, donations and collections including specialized collections. * Ensure SANBS donor clinic compliance to relevant legislation including the National Health Act. * Provide effective and timely medical support to the Zones, in...
The person will be responsible for the following: * Provide clinical oversight, timely medical advice and ensure implementation of all medical matters relating to blood donors, donations and collections including specialized collections. * Ensure SANBS donor clinic compliance to relevant legislation including the National Health Act. * Provide effective and timely medical support to the Zones, in...
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...
Position Purpose:To facilitate the setting of quality standards, policies, and procedures (clinical and non-clinical) for area. Ensure adherence to audit requirements, reporting and planning through evaluation, and coaching internal resources.Experience:5 years' experience in the Managed Care environment in pre-authorisation call centre/ hospital case management or hospital claims. Working experi...
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...
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...
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...
Position Purpose: To facilitate the setting of quality standards, policies, and procedures (clinical and non-clinical) for area. Ensure adherence to audit requirements, reporting and planning through evaluation, and coaching internal resources. Experience: 5 years experience in the Managed Care environment in pre-authorisation call centre/ hospital case management or hospital claims. Working expe...
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...
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...
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