GSK Hiring PVASC Specialist I in Bengaluru
![GSK Hiring PVASC Specialist I in Bengaluru 1 GSK: Hiring PVASC Specialist I in Bengaluru](https://pharmastuff.org.in/wp-content/uploads/2024/02/gsk-is-hiring-join-the-team-as-a-pvasc-specialist-i-in-bengaluru-1024x768.webp)
- GSK is Hiring! Join the Team as a PVASC Specialist I in Bengaluru
- About GSK
- Current Vacancies at GSK
- Job Description and Responsibilities
- Qualifications and Requirements
- How to Apply
GSK is Hiring! Join the Team as a PVASC Specialist I in Bengaluru
About GSK
GSK is a global biopharma company with a special purpose – to unite science, technology, and talent to get ahead of disease together. We’re currently seeking a dedicated PVASC Specialist I for our office in Bengaluru, Karnataka, India.
Current Vacancies at GSK
We are currently hiring for the position of PVASC Specialist I. This role provides an exceptional opportunity for professionals looking to advance their career in the pharmaceutical industry.
Job Description and Responsibilities
As a PVASC Specialist I, your responsibilities will include:
- Monitoring compliance with PVASC by carrying out routine reconciliations and compliance checks.
- Monitoring compliance with regulatory and internal quality of global adverse event reporting.
- Maintaining information in the pharmacovigilance database, Electronic Data Management System (EDMS), PVASC website pages, and shared areas.
- Collecting, evaluating, analyzing, and documenting information received from local operating company safety departments.
- Administering document storage and archiving according to approved processes.
- Representing GSK during both external regulatory inspection and GSK audits of licensing partners.
- Providing inputs to and maintaining guidance documents and SOPs.
- Contributing to and leading projects relating to improvements in processes and systems.
Role: PVASC Specialist I
Industry Type: Pharmaceuticals
Employment Type: Full Time
Job Location: Bengaluru, Karnataka, India
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Qualifications and Requirements
- Bachelor/Master degree (scientific or medically related field is preferred)
- A minimum of 5-7 years of working experience in the pharmaceutical industry in clinical development, pharmacovigilance, and information management or equivalent work experience.
How to Apply
Interested candidates are encouraged to apply online Click here
To apply for this job please visit jobs.gsk.com.
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