Reference: DBN000832-AD-2 Our Client, 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 Va...
Reference: DBN000832-AD-2 Our Client, 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 Va...
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...
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...
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...
Job DescriptionYou will join a widespread, yet closely-knit team with the same mentality and desire to develop smart and intelligent approach to project monitoring. You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. You will spend time monitoring study data remotely, identifying errors and issues with site performance. Office-based...
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...
Aculocity is a dynamic and innovative IT Services company committed to leveraging cutting-edge Artificial Intelligence (AI) and Machine Learning (ML) technologies to drive business growth and excellence. We are seeking a talented and experienced Chief Data Officer with strongAI/ML background to lead our AI/ML initiatives and contribute to our vision of becoming a leader in our industry.The Chief ...
Aculocity is a dynamic and innovative IT Services company committed to leveraging cutting-edge Artificial Intelligence (AI) and Machine Learning (ML) technologies to drive business growth and excellence. We are seeking a talented and experienced Chief Data Officer with strongAI/ML background to lead our AI/ML initiatives and contribute to our vision of becoming a leader in our industry.The Chief ...
Reference: PE000189-JD-1 The hiring organisation offers a minimum six-month fixed term contract opportunity to an experienced Registered Nurse with private hospital nursing experience. Ideally you will be based in Port Elizabeth, EC but the possibility exists of a candidate being based in Durban, Bellville or Centurion. ROLES AND RESPONSIBILITIES: Reporting to the Team Leader, your performance ar...
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...
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 Description:Designs or modifies data models to solve complex database requirements considering business and application needs. Organizes metadata for use by teams.(ads1)Job Responsibilities:Coordinates testing and documentation of the global metadata repository and conducts user interviews to gather metadata requirements to insure business requirements are met.Assists with creating and mainta...
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...
Essential Qualifications and Experience MBChB degree or Postgraduate qualification as a Professional Nurse with primary healthcare specialty (Nurse Clinician) Minimum 3 years post community service clinical experience (for medical doctors) and 8 years for Nurse Clinicians At least 2 years experience in a management or senior role within comprehensive HIV/TB programmes Understanding of TB/HIV/PMTC...
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...
IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.Data Team Lead, h...
Job Description:Designs or modifies data models to solve complex database requirements considering business and application needs. Organizes metadata for use by teams.(ads1)Job Responsibilities:Participates in enterprise-wide logical data modeling and leads efforts on assigned data subject areas.Participates in the implementation and management of the global metadata repository.Assists with creat...
Reference: PE000189-JD-1 The hiring organisation offers a minimum six-month fixed term contract opportunity to an experienced Registered Nurse with private hospital nursing experience. Ideally you will be based in Port Elizabeth, EC but the possibility exists of a candidate being based in Durban, Bellville or Centurion. ROLES AND RESPONSIBILITIES: Reporting to the Team Leader, your performance ar...
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