Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Pharmacovigilance Associate - Mid Shift

Pharmiweb
pharmiweb
1-3 years
Not Disclosed
Philippines, Remote
10 Feb. 19, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Pharmacovigilance Associate – Mid Shift (Home-Based)

Location: Philippines (100% Remote)
Company: ICON Strategic Solutions
Job Reference: JR135319
Industry: Clinical Research / Pharmacovigilance / Drug Safety
Employment Type: Full-Time
Shift: Mid Shift (4:00 PM – 1:00 AM PHT)
Experience Required: Minimum 1–3 years in Pharmacovigilance or Drug Safety
Education: Bachelor’s degree in Life Sciences, Pharmacy, or related field (Advanced degree preferred)
Application Deadline: 19 March 2026

ThePharmaDaily.com is featuring an excellent remote opportunity for a Pharmacovigilance Associate – Mid Shift with ICON Strategic Solutions, part of ICON plc, a globally recognized healthcare intelligence and clinical research organization.

This position is ideal for pharmacovigilance professionals seeking international exposure in drug safety operations while working in a fully home-based setup aligned with global timelines.

Role Overview

The Pharmacovigilance Associate will support global safety monitoring activities by collecting, reviewing, and reporting adverse event information in compliance with international regulatory standards. The role requires strong attention to detail, regulatory knowledge, and the ability to work independently in a remote environment.

This position follows a mid-shift schedule (4:00 PM – 1:00 AM PHT) to support global clinical and regulatory operations.

Key Responsibilities

  • Collect, review, and process adverse event (AE) reports in accordance with global pharmacovigilance regulations and internal SOPs

  • Ensure timely and accurate case documentation and regulatory reporting

  • Support signal detection and risk assessment activities to identify potential safety concerns

  • Assist in the preparation of safety reports and regulatory submissions

  • Collaborate with cross-functional teams including clinical, regulatory, and medical affairs

  • Maintain compliance with ICH guidelines, GVP requirements, and international safety standards

  • Stay updated with evolving pharmacovigilance regulations and industry best practices

Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, or related discipline (Master’s preferred)

  • Minimum 1–3 years of experience in pharmacovigilance, drug safety, or clinical safety operations

  • Working knowledge of adverse event case processing and safety databases

  • Understanding of global pharmacovigilance regulations (ICH, GVP, and applicable health authority guidelines)

  • Strong analytical skills with high attention to detail

  • Excellent written and verbal communication skills

  • Ability to work independently in a fully remote environment

  • Willingness to work mid shift (4 PM – 1 AM PHT)

  • Strong commitment to data confidentiality and regulatory compliance

Work Model

  • Fully home-based position in the Philippines

  • Mid shift schedule aligned with global operations

  • Collaborative engagement with international teams

Compensation and Benefits

ICON offers a competitive salary package along with country-specific benefits focused on employee well-being and work-life balance. Benefits may include:

  • Annual leave entitlements

  • Comprehensive health insurance options

  • Retirement planning programs

  • Global Employee Assistance Program

  • Life assurance

  • Flexible optional benefits such as wellness programs and subsidized services (as applicable)

Equal Opportunity Employer

ICON is committed to fostering an inclusive and discrimination-free workplace. All qualified applicants will receive equal consideration regardless of background or protected status.

This opportunity is ideal for early- to mid-career pharmacovigilance professionals seeking remote drug safety roles within a leading global clinical research organization.a