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PV specialist

Remote: 
Full Remote
Contract: 
Full time
Experience: 
Junior (1-2 years)
Work from: 
United Kingdom

Offer summary

Qualifications:

Minimum 1 year experience in Pharmacovigilance, Knowledge of Individual Case Safety Report submissions, Strong understanding of PV processes and regulations, Excellent organizational skills and attention to detail.

Key responsabilities:

  • Perform and manage PV activities
  • Handle and submit ICSRs accurately and timely
  • Collaborate with teams to ensure compliance
  • Maintain high patient safety standards and data quality
Luminary Group logo
Luminary Group Startup https://luminarygroup.co.uk/
2 - 10 Employees
About Luminary Group
Luminary Group is a Global Executive Search and Headhunting business specialising within the Life Sciences and Pharmaceutical space, headquartered in Broadgate Tower, 20 Primrose Street, EC2A 2EW, London. Finding premium candidates globally. We specialise in the Pharmaceutical, Biotechnology, CDMO, CRO & Medical Devices disciplines with local expertise and specialist knowledge. Specifically headhunting candidates for specialist roles across Board, Executive, Commercial, Operations, Medical, IT and Finance. With global coverage across USA, Europe, APAC, and Middle East, we pride ourselves in both our outstanding talent pool (ranging from C-Suite to Manager level) and our returning clients who work with us exclusively. Partnered with the best, and most exciting, companies ranging from Corporate to Start-Up businesses. We are Luminary. You are Luminary.
See more Luminary Group offers

Job description

We are seeking Pharmacovigilance Specialists to join our team for an upcoming project with a global pharmaceutical company. The ideal candidates should bring at least one year of experience in Pharmacovigilance and have a solid understanding or hands-on experience with Individual Case Safety Report (ICSR) submissions.

Key Responsibilities:

  • Perform and manage Pharmacovigilance activities, including the review and analysis of safety data.
  • Handle Individual Case Safety Reports (ICSRs) and ensure accurate and timely submissions.
  • Collaborate with cross-functional teams to maintain compliance with regulatory requirements.
  • Contribute to maintaining high standards of patient safety and data quality.

Qualifications:

  • Minimum of 1 year of experience in Pharmacovigilance.
  • Knowledge or experience with Individual Case Safety Report (ICSR) submissions.
  • Strong understanding of Pharmacovigilance processes and regulatory requirements.
  • Excellent organizational skills and attention to detail.

Additional Information:

  • Start Date: August 15th
  • Workload: 35-40 foreign cases per day, with potential for local cases.
  • Environment: Fast-paced and dynamic setting within a leading global pharmaceutical company.

If you meet these qualifications and are interested in a challenging and rewarding role, please apply or reach out to discuss further.

 

Required profile

Experience

Level of experience: Junior (1-2 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.
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