Case Specialist Philippines 2

PLG; Philippines; On-site; PHP 480,000 - 800,000; Full time

Job summary

ProductLife Group Philippines is seeking a Case Specialist (Pharmacovigilance) to ensure high-quality handling of vigilance cases and data entry across client databases. The role requires solid knowledge of GVP/GCP and regulatory requirements as well as strong collaboration with a global team.

The successful candidate will perform medical evaluations, coding, causal assessment, and case closure, while meeting deadlines and maintaining rigorous documentation in post-marketing activities.

Qualifications

• Doctor in Pharmacy or pharmacist by training.
• Minimum 3 years in a similar role.
• Experience meeting deadlines.
• Pharmacovigilance knowledge and post-marketing case processing.

Responsibilities

• QC of vigilance cases.
• Medical evaluation of reports.
• Data entry of vigilance cases in databases.
• Follow-up requests by phone/mail.
• Pre-analysis of complex cases prior to data entry.
• Causality assessment and coding per dictionaries.
• Close vigilance files and prepare regulatory documentation.
• Identify submission requirements and maintain QA for documents.

Skills

Pharmacovigilance

Database experience

GVP/GCP knowledge

Regulatory knowledge

Microsoft Office

Multitasking

Communication skills

Teamwork

Pharmacist

Education

Doctor in Pharmacy

Tools

Microsoft Office

Databases

Job description

## Case Specialist Philippines 2Apply: Remote: No Office - Philippine based: Full time: Posted 11 Days Ago: End Date: December 31, 2026 (30+ days left to apply): JR000048Make a meaningful impact on global healthcare — and grow your career while doing it. At ProductLife Group, you’ll join an innovative, forward‐thinking team operating across the world to shape the future of life sciences through expertise, collaboration, and purpose‐driven work.**Job Description :**ProductLife Group is looking for **Case Specialist (Pharmacovigilance)** to join and contribute to the activities of the hub.**Responsibilities:**Responsible for the Quality control of vigilance cases Medical evaluation of reportsData entry of vigilance cases in ad hoc databases or in other formats agreed with the clientFollow-up request of vigilance cases by phone/mailPre-analysis of complex cases prior to data entryMedical evaluation of files on:* Coding (according to applicable dictionary)* Causal relationship between the effects and the intake of suspect products (according to applicable method)* The expected/listed or unlisted nature of the events/effects/incidents* The seriousness of the events/effects/incidents and the caseIdentification of submission requirements for each caseValidation of certain documents produced by the Data Manager/ Vigilance Associate / documentalist (phone call forms, etc)Closing of vigilance filesIdentification of requirements and applicable changes to set up ICSR/MLM filtersAnalysis of inclusion / exclusion of EV/MHRA cases To perform QC for clinical/post-marketing casesKey Contact for specific customers (with the support of an Activity Manager or the Line Manager)**Education & Experience:*** Doctor in Pharmacy/ Pharmacist by training* Minimum 3 years of experience in a similar position* Previous experience working to deadlines* Database experience* Clinical and Post Marketing case processing experience* Pharmaceutical background – strong understanding of GVP, GCP, FDA and regulatory requirements related to drug safety.* Deep knowledge of pharmacovigilance principles, adverse event reporting, causality assessment.**Skills:*** Database experience preferred* Knowledge of current regulations* Process oriented* Rigorous and ability to work in a team* Use of Microsoft Office tools* Ability to multitask* Flexibility* Excellent communication skillsReady to take the next step? Apply today and join a global, innovative team that’s shaping the future of life sciences and empowering people to make a real impact in healthcare.