Clinical Research Associate

With support of other Clinical Research Managers and/or Therapeutic Area Head/Clinical Research Director, this role is accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or Clinical Research Director, the person ensures compliance of study conduct with ICH/Good Clinical Practice and country regulations, our company's policies and procedures, quality standards and adverse event reporting...

Clinical Research Director**Job Summary**MNA Recruitment (Pty) Ltd is seeking an experienced Clinical Research Director to lead Clinical Operations for South Africa and the Sub-Saharan Cluster. The ideal candidate will have a strong background in clinical trials, excellent leadership skills, and the ability to shape the clinical research landscape.**Key...

**Brief Description of Position** With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical...

**Brief Description of Position** The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, the organization's policies and procedures, quality standards and adverse event reporting...

**Brief Description of Position** The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, organizational policies and procedures, quality standards and adverse event reporting...

Join our cutting-edge Clinical Research team that is dedicated to enhancing global healthcare through groundbreaking research and innovation. As the **Executive Director of Clinical Research**, you will spearhead Clinical Operations in **South Africa and the Sub-Saharan Cluster**, overseeing the execution of all clinical trials within the region. You will...

**Job Title:** Clinical Research Director**About the Role:** MNA Recruitment (Pty) Ltd is seeking a highly skilled Clinical Research Director to lead Clinical Operations for South Africa and the Sub-Saharan Cluster.The ideal candidate will have a deep understanding of clinical trials and a proven track record of leadership in the pharmaceutical...

This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adherence to local regulations, company SOPs and ICH GCP. As line manager the role is critical to...

A Global Pharmaceutical Company is seeking an Executive Director, Clinical Research South Africa and Sub-Saharan Cluster to join their team.As the Executive Director of Clinical Research, the individual will lead Clinical Operations for South Africa and the Sub-Saharan Cluster, overseeing all Clinical Trials. They will play a crucial role in shaping the...

This role is primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. For certain studies, the Clinical Research Manager could be...

This role is primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. For certain studies, the Clinical Research Manager could be...

This role is primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. For certain studies, the Clinical Research Manager could be...

It is critical that, for all Organisation-sponsored clinical trials, patient safety, high quality data and compliance with company requirements and regulations are delivered and sustained. The Associate CCQM position has an important impact in achieving those objectives. Under the guidance of the Regional Director, Clinical Quality Management (RCQM) and in...

**Brief Description of Position**: This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD,...

**Brief Description of Position**: This role is accountable for performance and compliance for assigned protocols in **SOUTH AFRICA and OTHER AFRICAN COUNTRIES** in compliance with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight...

Under the guidance of the Regional Director, Clinical Quality Management (RCQM) and in close collaboration with the Country Clinical Quality Manager (CCQM), the Associate CCQM supports the oversight of specific CQM activities in the respective country/cluster. The role requires the ability to properly support the implementation of local/global processes /...

**Are you passionate about healthcare and innovation? Do you have a detail-oriented mindset and a desire to make a difference in people's lives? If so, we invite you to join us as a Senior Clinical Trial Coordinator. This vital role in our research & development division allows you to contribute directly to our premier mission of delivering innovative health...

This role is accountable for performance and compliance for assigned protocols in South Africa and Other African Countries in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the COM lead, Head COMs or CRD, you...

This role is accountable for execution and oversight of local operational clinical trial activities in compliance with ICH/GCP and country regulations, our Company's policies and procedures and with quality standards internally and externally. The person has ownership, oversight and impact on study operational activities and for out-tasking as applicable....