Pharmacovigilance Intern

2 weeks ago

Midrand, South Africa ITrain Full time

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 knowledge of Global, Regional and Local PV Procedural Documents as applicable.
6. Proven ability to manage projects as assigned and to work unsupervised.

Special Requirements
Fluency in local language(s) and in the English language is required.
Proficiency in Medical terminology (local languages).

**Job Types**: Full-time, Internship
Contract length: 12 months

**Salary**: R7,000.00 per month

**Education**:

- Bachelors (required)

Expected Start Date: 2024/01/01

  • Pharmacovigilance Manager

    3 days ago

    Midrand, South Africa Metamorphosis Integrated Solutions Full time

    **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...

  • Associate Clinical Research Manager

    1 day ago

    Midrand, South Africa MSD Full time

    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...

  • Clinical Research Manager

    2 weeks ago

    Midrand, South Africa MSD Full time

    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...

  • Regulatory Affairs Pharmacist

    3 days ago

    Midrand, South Africa MSD Full time

    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...

  • Clinical Operations Manager

    6 days ago

    Midrand, South Africa MSD Full time

    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...