Pharmacovigilance Officer in Hartley Wintney

Pharmacovigilance Officer in Hartley Wintney

Hartley Wintney Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage pharmacovigilance activities and ensure compliance with regulatory requirements.
  • Company: Join a leading company in the pharmaceutical industry with a focus on safety.
  • Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
  • Why this job: Make a real difference in patient safety while working in a dynamic environment.
  • Qualifications: Experience in pharmacovigilance and strong attention to detail required.
  • Other info: Collaborative team culture with opportunities for career advancement.

The predicted salary is between 36000 - 60000 £ per year.

Experienced Pharmacovigilance Officer (Hybrid role). This is NOT an entry level role. 3 month initial Fixed Term Contract. Immediate start preferred.

The Pharmacovigilance Officer has responsibility for the conduct and delivery of Pharmacovigilance activities on assigned projects, management and oversight of incoming information, as well as input to the development and maintenance of TMC PV systems. Integral to the PV department’s day-to-day operational tasks, the PV Officer will be responsible for a variety of pharmacovigilance activities. These will include safety database administration, PV case processing related work, such as the triage and data entry of incoming PV information (e.g. processing individual case safety reports – ICSRs), management of PV eTMF filing, communication with clients on key deliverables (project dependent). The PV officer will need to comply with the applicable regulatory requirements (e.g. GVP) as well as work to TMC’s SOPs, both in relation to clinical trials and with marketed products.

THIS IS A HYBRID ROLE: we expect the successful candidate to be able to come to the office in Hartley Wintney, Hampshire, regularly.

Role-specific tasks include:

  • Maintenance of SAE/SUSAR/AESI trackers
  • Argus safety database administration
  • ICSR case processing including triage, data entry, quality control and submission
  • Issuing and tracking ICSR queries
  • Working with PV physician to co-ordinate medical review of cases and drafting of analysis of similar events (AOSEs) as required
  • Coding Adverse Events and the medicines/treatments recorded on the Adverse Drug Reaction and Serious Adverse Event reports, according to MedDRA & WHODrug standards
  • Supporting SAE reconciliation with clinical databases and eTMF filing, as required
  • Liaising with the Sponsor / MA Holder on expediting Adverse Event reports as required
  • Organising and minuting TMC project team meetings
  • Building and maintaining good relationships across all TMC functional units
  • Provide input and support to TMC to ensure compliance (including monitoring of departmental metrics) with current PV regulatory requirements
  • Supporting PV audit and inspection activities, as required
  • Other duties as assigned by management (e.g. supporting signal detection activities, PSMF updates etc.)

Pharmacovigilance Officer in Hartley Wintney employer: T M C Pharma Services Ltd

At TMC, we pride ourselves on being an exceptional employer, offering a dynamic work environment in Hartley Wintney that fosters collaboration and innovation. Our hybrid role for a Pharmacovigilance Officer not only provides competitive benefits and a supportive culture but also encourages professional growth through continuous learning opportunities and engagement with cross-functional teams. Join us to make a meaningful impact in the field of pharmacovigilance while enjoying the unique advantages of working in a vibrant community.
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Contact Detail:

T M C Pharma Services Ltd Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Pharmacovigilance Officer in Hartley Wintney

✨Tip Number 1

Network like a pro! Reach out to professionals in the pharmacovigilance field on LinkedIn or at industry events. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream role.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of GVP and TMC’s SOPs. We recommend practising common interview questions related to pharmacovigilance activities so you can showcase your expertise confidently.

✨Tip Number 3

Don’t forget to follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. We suggest mentioning something specific from the interview to make it personal.

✨Tip Number 4

Apply through our website for the best chance of getting noticed! We’re always on the lookout for passionate candidates who are ready to dive into the world of pharmacovigilance. Let’s get you started on this exciting journey!

We think you need these skills to ace Pharmacovigilance Officer in Hartley Wintney

Pharmacovigilance
Safety Database Administration
ICSR Case Processing
Data Entry
Quality Control
Regulatory Compliance (GVP)
SOP Adherence
Adverse Event Coding (MedDRA & WHODrug)
SAE/SUSAR/AESI Tracking
Communication Skills
Project Coordination
Relationship Management
Audit and Inspection Support
Signal Detection Activities

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Pharmacovigilance Officer role. Highlight relevant experience and skills that match the job description, especially in safety database administration and case processing.

Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this hybrid role. Share specific examples of your past work in pharmacovigilance and how you’ve contributed to compliance and operational tasks.

Showcase Your Attention to Detail: Since this role involves a lot of data entry and quality control, make sure to demonstrate your attention to detail in your application. A well-structured CV and error-free cover letter will show us you mean business!

Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and keep track of it, so don’t miss out on this opportunity!

How to prepare for a job interview at T M C Pharma Services Ltd

✨Know Your Pharmacovigilance Basics

Make sure you brush up on your pharmacovigilance knowledge, especially around GVP and SOPs. Familiarise yourself with the key responsibilities of a Pharmacovigilance Officer, such as ICSR processing and safety database administration. This will show that you're not just interested in the role but also understand its complexities.

✨Prepare for Scenario-Based Questions

Expect to be asked about specific scenarios related to adverse event reporting or case processing. Think of examples from your past experience where you successfully managed similar tasks. This will help demonstrate your practical knowledge and problem-solving skills.

✨Showcase Your Communication Skills

As a Pharmacovigilance Officer, you'll need to liaise with various stakeholders. Be ready to discuss how you've effectively communicated with clients or team members in previous roles. Highlight any experiences where you’ve had to explain complex information clearly and concisely.

✨Ask Insightful Questions

At the end of the interview, don’t forget to ask questions! Inquire about the team dynamics, ongoing projects, or how they ensure compliance with regulatory requirements. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Pharmacovigilance Officer in Hartley Wintney
T M C Pharma Services Ltd
Location: Hartley Wintney
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