Pharmacovigilance Specialist, Case Processing

ProPharma Group; United Kingdom; Hybrid; GBP 32,000 - 54,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

ProPharma Group is seeking a Pharmacovigilance Specialist, Case Processing in the United Kingdom. The role focuses on daily AE case processing, MedDRA coding, and ensuring accurate case narratives. Hybrid working is supported, with option to work remotely part of the week.

Ideal candidates have a life sciences degree and about two years of PV or related experience, strong communication, and meticulous attention to detail to maintain high-quality safety data for clients.

Qualifications

• Bachelor's degree in life sciences required.
• Two years of related PV or case processing experience.
• Basic knowledge of pharmacovigilance concepts.
• Excellent written and verbal communication skills.
• Ability to work both independently and in a cross-functional team.

Responsibilities

• Handle daily case processing of adverse event reports (clinical trial and post-marketed).
• Code events using MedDRA and assess seriousness and expectedness at case level.
• Perform follow-up to collect necessary information.
• Prepare case narratives and provide client notifications as needed.
• Support development of PV training materials and training delivery.

Skills

Verbal and written communication

Attention to detail

Problem solving

Independent and collaborative work

Organization and multitasking

Pharmacovigilance knowledge

Education

Bachelor's degree in life sciences

Job description

Pharmacovigilance Specialist, Case Processing# Careers## Pharmacovigilance Specialist, Case ProcessingApply: Serbia (DNU!): Bosnia (DNU): United Kingdom: Croatia (DNU): Full time: Posted 2 Days Ago: JR 10896For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.**Essential Functions:*** Responsible for daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level.* Perform case follow up activities such as identification of information to be collected during follow-up.* Creating and reviewing case narratives.* Providing client notifications as required for case management.* Supporting and contributing to the development of training materials and training delivery.* Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing and/or Manager, Case Processing when related to ICSRs.* Acquire and maintain an up-to-date knowledge of global safety regulations for medicines.* Peer reviews of cases for quality, consistency, and accuracy as needed.* Other duties as assigned**Necessary Skills and Abilities:*** Strong verbal, written and interpersonal communication skills.* High level of accuracy and attention to detail.* Ability to identify and resolve problems in a timely manner.* Able to work independently and collaboratively in a multi-disciplinary team.* Excellent organization and prioritization skills; able to multitask.* Basic knowledge of Pharmacovigilance.**Educational Requirements:*** Required: a Bachelor's degree in life sciences.* Preferred: advanced degree, RN, RPh, PharmD or equivalent.**Experience Requirements:**Two years of related work experience.We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.\\*\\*\\*ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.\\*\\*\\*