Senior Pharmacovigilance Specialist, case processing

ProPharma Group; Makati; On-site; PHP 600,000 - 900,000; Full time

Job summary

ProPharma Group is seeking a Senior Pharmacovigilance Specialist to oversee daily adverse event case processing, including MedDRA coding and case narratives, in a hybrid setup based in Makati. The role emphasizes accuracy, client communication, and adherence to global PV regulations.

The ideal candidate has a life sciences degree with PV experience, strong analytical skills, and the ability to mentor junior staff, while participating in ongoing PV trainings and process improvements.

Qualifications

• Bachelor's degree in life sciences required.
• Advanced degree (RN/RPh/PharmD) preferred.
• Three years of related work experience in pharmacovigilance or case processing.
• Knowledge of MedDRA coding and PV regulatory requirements.

Responsibilities

• Oversee daily case processing of adverse event reports (clinical trial and post-marketed).
• Code using MedDRA and determine seriousness and expectedness at event and case level.
• Prepare and review case narratives and follow-up activities.
• Provide client notifications and contribute to PV training materials.

Skills

Verbal and written communication

Project management (intermediate)

Attention to detail

Problem solving

Team collaboration

Multitasking

Pharmacovigilance knowledge

PV systems knowledge (Oracle Argus/ARi

Education

Bachelor's degree in life sciences

Advanced degree (RN/RPh/PharmD)

Tools

Oracle Argus Safety

ARISg

Job description

## Senior Pharmacovigilance Specialist, case processingApplylocations: Makati Citytime type: Full timeposted on: Posted Yesterdayjob requisition id: JR 10190For 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 overseeing and performing 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.* Provide oversight and direction of PV deliverables as a PV subject matter expert as needed.* Perform Health Care Professional (HCP) review (as required).* Mentors and trains less experienced staff.* Other duties as assigned.**Necessary Skills and Abilities:*** Strong verbal, written and interpersonal communication skills.* Intermediate project management 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.* Intermediate knowledge of Pharmacovigilance.* Working knowledge of PV Systems, such as Oracle Argus Safety, ARISg, or other safety databases.**Educational Requirements:*** Required: a Bachelor's degree in life sciences.* Preferred: an advanced degree, RN, RPh, PharmD or equivalent.**Experience Requirements:*** Three years of related work experience.#LI-FDT1We 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.\*\*\*