Pharmacovigilance Intern

Reporting to Head: Medical AffairsJob PurposeTo provide quality Pharmacovigilance (PV) Management expertise by effectively overseeing all The Client processes related to drug safety surveillance and response, ensuring compliance with the relevant laws/ regulations and guidelines, as well as internal policies that govern pharmacovigilance practices in each...

Please note, this role is a 2-year contracting position.The PV Intern is responsible for undertaking specified PV activities, including projects, with oversight by their manager or a designated PV colleague.Specific details of tasks may be further described in an addendum to this job description. Activities listed below are applicable for all supported...

Relevant skills required include:Good verbal and written communication skills with knowledge of medicalterminology.Strong organizational skills, attention to detail and accuracy are important.and resources.Able to build and maintain a network of company contacts and resources to support the Local Safety Unit and its objectives.Acquires knowledge of Global,...

Your responsibilities include, but not limited to:Leadership:Build strong relationships with relevant functions in the affiliate organization (including but not limited to regulatory affairs, medical affairs, quality assurance, marketing and sales, clinical development and others), in collaboration with the Director Patient Safety HUB/ Associated Director...

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...

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 PositionThis role will be key to further develop the...

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 Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and...

Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance partnering with external regulatory agencies. We are on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the...

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.It is critical that, for all company-sponsored clinical trials, patient...

Job DescriptionThe 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 Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally...

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 Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally....

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...

Job DescriptionThe 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 Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally...

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 of the Sr....

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, the...

Company DescriptionJob Description PRIMARY FUNCTION**:Pipeline MSLs serve to enhance the scientific credibility of the Company with established and emerging clinical investigators_ _as well as key scientific institutions and collaborative study groups, by supporting scientific dialogue and collaborations in the areas of research, medical and scientific...

Job DescriptionBrief 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, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the COM Lead, Head COMs or...

Job DescriptionBrief 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, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the COM Lead, Head COMs or...

Job DescriptionThis 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...

**Reporting to Head**: Medical Affairs Job Purpose To provide quality Pharmacovigilance (PV) Management expertise by effectively overseeing all The Client processes related to drug safety surveillance and response, ensuring compliance with the relevant laws/ regulations and guidelines, as well as internal policies that govern pharmacovigilance practices in...

**Please note, this role is a 2-year contracting position.** **The PV Intern** is responsible for undertaking specified PV activities, including projects, with oversight by their manager or a designated PV colleague. **Specific details of tasks may be further described in an addendum to this job description. Activities listed below are applicable for all...

Relevant skills required include: 1. Good verbal and written communication skills with knowledge of medical terminology. 2. Strong organizational skills, attention to detail and accuracy are important. and resources. 4. Able to build and maintain a network of company contacts and resources to support the Local Safety Unit and its objectives. 5. Acquires...

Relevant skills required include: 1. Good verbal and written communication skills with knowledge of medical terminology. 2. Strong organizational skills, attention to detail and accuracy are important. and resources. 4. Able to build and maintain a network of company contacts and resources to support the Local Safety Unit and its objectives. 5. Acquires...

**Midrand, Gauteng, Africa**: As a **Medical Manager**, you will help guide the strategic direction in therapeutic areas and provide training and support to the sales force. Provide information regarding medical based questions, legal and regulatory matters, thus enabling colleagues to comply with the required statutory requirements. Develop good...

Your responsibilities include, but not limited to: - **Leadership**:Build strong relationships with relevant functions in the affiliate organization (including but not limited to regulatory affairs, medical affairs, quality assurance, marketing and sales, clinical development and others), in collaboration with the Director Patient Safety HUB/ Associated...

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...

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...

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...

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 Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and...

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 Good Clinical Practice and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and...

Minimum Requirements Grade 12 BPharm degree At least 6 years of experience in QC Manufacturing experience Knowledge of cGMP principles Understanding of legislation for Manufacturing Pharmacy and regulatory processes Duties and Responsibilities: Manage product launch after successful completion of safety, efficacy, and quality testing Pharmacovigilance...

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. It is critical that, for all company-sponsored clinical trials, patient...

Minimum RequirementsGrade 12BPharm degreeAt least 6 years of experience in QCManufacturing experienceKnowledge of cGMP principlesUnderstanding of legislation for Manufacturing Pharmacy and regulatory processesDuties and Responsibilities:Manage product launch after successful completion of safety, efficacy, and quality testingPharmacovigilance and handle...

Minimum RequirementsGrade 12BPharm degreeAt least 6 years of experience in QCManufacturing experienceKnowledge of cGMP principlesUnderstanding of legislation for Manufacturing Pharmacy and regulatory processesDuties and Responsibilities:Manage product launch after successful completion of safety, efficacy, and quality testingPharmacovigilance and handle...

**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 policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the...

**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 a country in compliance with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the...

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...

**Roles & Responsibilities** - Operationally be involved with all aspects of the distribution processes and quality issues of the total company''s Warehouse organization. - Overall responsibility to ensure that ALL operations at The company are conducted according to the requirements of The Medicines and Related Substances Act (Act 101 of 1965), as amended,...