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Scientific Information Manager

Quanta Consultancy Services Ltd

England

On-site

GBP 45,000 - 75,000

Full time

30+ days ago

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Job summary

Join a leading international pharmaceutical organization as a Pharmacovigilance and Scientific Information Manager in Surrey. This exciting opportunity allows you to leverage your expertise in pharmacovigilance while working in a dynamic and passionate team. You will be responsible for overseeing UK PV cases, ensuring compliance with health authorities, and maintaining the pharmacovigilance system master file. The role offers a competitive salary and an additional benefits package in an international working environment that promotes continuous learning and development. If you are looking to make a significant impact in the pharmaceutical industry, this is the perfect role for you.

Benefits

Competitive salary
Additional benefit package
Continuous Learning & Development opportunities
International working environment

Qualifications

  • 5-10 years of experience in pharmacovigilance is required.
  • A life science degree or health professional qualification is essential.

Responsibilities

  • Oversee all UK pharmacovigilance cases and ensure compliance.
  • Act as primary contact for the MHRA and maintain the PSMF.

Skills

Pharmacovigilance
Regulatory Compliance
Line Management
Health Sciences

Education

Life Science Degree
Qualified Health Professional

Job description

Pharmacovigilance and Scientific Information Manager - Surrey - Permanent

Do you want the opportunity to work with an international pharmaceutical organisation based in Surrey? If yes, then this is the assignment for you!

Our client, who specializes in producing generic pharmaceutical products for patients across the globe, is currently seeking the expertise of a Pharmacovigilance and Scientific Information Manager.

Our client offers:

  1. Competitive salary;
  2. Additional benefit package;
  3. International working environment and a passionate team of professionals;
  4. Continuous Learning & Development opportunities.

Responsibilities:

  1. Maintain oversight of all UK PV cases (including cases received via health authorities).
  2. Act as the primary PV contact person for the MHRA.
  3. Monitor compliance of UK PV case and aggregate report submissions.
  4. Author and maintain the UK pharmacovigilance system master file (PSMF).
  5. Ensure that the UK Qualified Person for pharmacovigilance (QPPV) is kept fully aware of all UK PV specific information.
  6. Be registered with and accessible to MHRA 24/7 in case of urgent safety situations.

Requirements:

  1. Life science degree or qualified Health Professional (e.g. pharmacy technician, pharmacist, nurse).
  2. 5-10 years’ experience within pharmacovigilance.
  3. Previous line management responsibilities would be advantageous.

If this role is of interest to you, please apply now!

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