Country Clinical Quality Manager

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...

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...

**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 SCOM, the person is...

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. Brief Description of Position This role is primarily accountable for the...

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. Clinical Operations Manager, Head COMs or...

**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,...

Job DescriptionThis 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, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally.For certain studies, the CRM could be...

Job DescriptionThis role is accountable for the end-to-end performance and project management of assigned protocols in a country, ensuring compliance with ICH/GCP and country regulations. The successful candidate will proactively plan, drive, and track the execution and performance of deliverables/timelines/results to meet country commitments.Main...

**Brief Description of Position**: Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools,...

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...

IDEXX reference laboratories is a global network united by a shared commitment to enhancing pet care where the true strength in our name is the people behind it. Our reference laboratories make it possible for our customers to discover more with our unrelenting commitment to innovation, personalized support, guidance, and expertise, while providing the most...

Job OverviewMerck Gruppe - MSD Sharp & Dohme seeks an experienced professional to lead the end-to-end performance and project management of assigned protocols in a country. The CRM will be responsible for ensuring compliance with ICH/GCP and country regulations, as well as collaborating with functional outsourcing vendors, investigators, and other external...

With support of Senior Clinical Research Associate/Clinical Research Associate and/or CRA Manager, the Associate CRA acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. Primary Responsibilities: - Develops strong site relationships and ensures continuity of site...

Founded in 1906 as a manufacturer of writing instruments, MONTBLANC today creates exclusive products including watches, jewelry, writing instruments and leather goods which reflect our high demands with respect to culture, quality, design, tradition and craftsmanship. With more than 25 subsidiaries and 600 boutiques MONTBLANC is present all over the...

Do you want to help shape the future of healthcare? Our name, Siemens Healthineers, was selected to honor our people who dedicate their energy and passion to this cause. It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry. We offer you a flexible and dynamic environment with...

Do you want to help shape the future of healthcare? Our name, Siemens Healthineers, was selected to honor our people who dedicate their energy and passion to this cause. It reflects their pioneering spirit combined with our long history of engineering in the ever-evolving healthcare industry. We offer you a flexible and dynamic environment with...

Company OverviewDis-Chem Pharmacies is a leading healthcare provider in South Africa, committed to delivering high-quality patient care and exceptional service. As a primary health care clinic sister, you will play a vital role in managing our Kyalami clinic, ensuring that patients receive the best possible care.

Job SummaryWe are seeking a skilled Clinical Research Manager to oversee the end-to-end performance and project management of assigned protocols in a country. This individual will be responsible for ensuring compliance with regulatory requirements, developing and implementing local risk management plans, and collaborating with stakeholders to drive business...

Job DetailsAs a Clinical Research Manager at Merck Gruppe - MSD Sharp & Dohme, you will be responsible for leading the end-to-end performance and project management of assigned protocols in a country. Key responsibilities include ensuring compliance with regulatory requirements, managing project timelines, and driving business growth through stakeholder...

The purpose of this job is to provide country risk reports inclusive of country risk ratings and LGD’s using the various rating tools to support the mandate of the DBSA to provide Cross Border Development assistance and lending. The Cross-Border functions are spread across the Coverage, Transacting and Project Preparation Divisions aimed at enhancing...