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Pharmacovigilance and medical information officer

Brighton
JR United Kingdom
Medical information officer
€100,000 - €125,000 a year
Posted: 1h ago
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Pharmacovigilance and Medical Information Officer, Brighton

Client: NEON HEALTHCARE LTD

Location: Brighton, United Kingdom

Job Category: Other

EU work permit required: Yes


Job Views:

3


Posted:

04.06.2025


Expiry Date:

19.07.2025


Job Description:

The role has been created to meet the continued growth of the business. We are now searching for an enthusiastic individual with great attention to detail, proactive and well-organised mindset to join our growing Pharmacovigilance and Medical Information team.

Please be aware this role is office based, our office is in Hertford, UK.


Role Responsibilities

* Responsible for developing and maintaining the AE reporting processes and system.
* Responding to Medical Information (MI) enquiries.
* Executing literature searches to identify key product articles.
* Creating and collating aggregate reports (PSURs, RMPs, Renewals, etc.).
* Performing reconciliation activities of received medical information enquiries, product complaints, and adverse events with internal and external stakeholders as required.
* Supporting the collation of PV/MI Compliance metrics, KPIs, and Quality Review reports.
* Providing support in preparation for internal and external audits.
* Keeping current with professional and pharmacovigilance regulations and knowledge.
* Identifying new training and development opportunities for the PV department.
* Ensuring all regulatory timeframes are met for safety information processing and reporting.
* Assisting in departmental project activities in accordance with SOPs, regulatory requirements, and contractual obligations.
* Reviewing safety tracking systems for accuracy and quality.
* Maintaining documentation in accordance with Good Documentation Practice.
* Liaising with partners and internal departments regarding safety issues.
* Coordinating interdepartmental activities such as listing review, quality control, audits, and inspections.
* Reviewing key study documentation for Pharmacovigilance inputs.
* Staying updated on safety regulations and guidelines.
* Performing additional duties as requested by management.
* Providing administrative support to the Pharmacovigilance team.
* Developing and maintaining knowledge of the company's products.
* Representing Pharmacovigilance and medical information in cross-functional meetings.


Key Skills, Knowledge, and Experience

* At least one year of relevant experience in the pharmaceutical industry preferred.
* Willingness to learn and grow with the team.
* BSc or equivalent in Life Sciences.
* Excellent communication skills in English.
* Strong planning and organizational skills with the ability to multitask.
* Flexible, proactive, and effective team worker.
* Attention to detail and ability to work under pressure.
* Ability to build relationships with internal and external customers.
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