Case Specialist Philippines 1

PLG; Philippines; Remote; PHP 500,000 - 900,000; Full time

Job summary

ProductLife Group is seeking a Case Specialist (Pharmacovigilance) to join our team in the Philippines. You will perform medical evaluations, data entry, and QA checks on vigilance cases, while coordinating with clients and internal teams to ensure timely and accurate case processing.

Ideal candidates hold a PharmD/Pharmacist degree with at least 3 years in pharmacovigilance, deep regulatory knowledge, and proficiency in MS Office. This is a full-time, on-site role based in the Philippines.

Qualifications

• Pharmacist by training with relevant degree.
• Minimum 3 years of experience in a similar pharmacovigilance role.
• Strong knowledge of GVP, GCP, FDA regulations and drug safety principles.

Responsibilities

• QC vigilance cases and medical evaluation of reports.
• Data entry of vigilance cases into databases.
• Follow-up with clients by phone or email.

Skills

Database experience

Regulatory knowledge

Process oriented

Team player

MS Office

Multitasking

Flexibility

Communication skills

Education

Pharmacist degree

Tools

Microsoft Office

Job description

## Case Specialist Philippines 1Apply: Remote: No Office - Philippine based: Full time: Posted 11 Days Ago: End Date: December 31, 2026 (30+ days left to apply): JR000047Make 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.