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Coordinator (Pharmacovigilance)

Product Life Group
Product Life Group
3-4 years
Not Disclosed
Remote
10 March 2, 2026
Job Description
Job Type: 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

Coordinator – Pharmacovigilance (Safety & Vigilance)

Location: India
Work Model: Remote (Work from Home Available)
Department: Life Cycle – Safety and Vigilance
Employment Type: Permanent

About the Role

ThePharmaDaily.com is hiring an experienced Pharmacovigilance Coordinator to support global drug safety operations within the Safety and Vigilance function. This remote opportunity in India is ideal for professionals with hands-on experience in pharmacovigilance workflow case management, regulatory compliance, and adverse event monitoring.

The selected candidate will play a critical role in monitoring workflow systems, optimizing case distribution, ensuring regulatory timelines are met, and maintaining compliance with global pharmacovigilance regulations including GVP and FDA requirements.

This role is suited for professionals with strong analytical skills, deep knowledge of drug safety regulations, and the ability to manage pharmacovigilance case processing workflows in a dynamic environment.

Key Responsibilities

  • Monitor real-time performance of pharmacovigilance workflow systems to ensure optimal resource allocation

  • Track case progress to maintain compliance with regulatory timelines and internal KPIs

  • Ensure appropriate assignment of safety cases to relevant individuals or functional teams

  • Collaborate with cross-functional teams including operations, regulatory, and development to align solutions with business and compliance requirements

  • Provide technical guidance and cross-training to team members

  • Investigate workflow issues and implement corrective and preventive actions under strict deadlines

  • Analyze workflow metrics and identify performance improvement opportunities

  • Support documentation, reporting, and process optimization initiatives

Eligibility & Qualifications

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

  • Strong understanding of global pharmacovigilance regulations, including GVP, FDA requirements, and cosmetic safety regulations

  • Deep knowledge of pharmacovigilance principles, adverse event reporting, and causality assessment

  • Experience in reading and interpreting Safety Data Exchange Agreements (SDEAs) and Pharmacovigilance Agreements (PVAs)

  • Proficiency in Microsoft Office tools (Excel, Word, PowerPoint)

  • Experience working with safety databases and workflow management systems

Experience Required

  • 3–4 years of hands-on experience in Pharmacovigilance workflow case management

  • Experience in safety operations within pharmaceutical, biotechnology, or CRO environments

Core Competencies

  • Strong analytical and problem-solving skills

  • Excellent organizational and time-management abilities

  • Effective communication and documentation skills

  • Project coordination and task prioritization capability

  • Ability to work independently in a remote setup

  • High level of accountability and decision-making ability

  • Team-oriented mindset with adaptability and reliability

Preferred Skills & Attributes

  • Database management experience

  • Emotional intelligence and cross-functional collaboration skills

  • Flexibility in handling multiple priorities

  • Strong attention to detail and punctuality

Why Apply Through ThePharmaDaily.com?

This opportunity is ideal for pharmacovigilance professionals seeking career advancement in global drug safety, regulatory compliance, and workflow optimization within a remote work model in India. The role offers exposure to international safety standards, lifecycle management processes, and strategic pharmacovigilance operations.

Application Process

Applications will be reviewed based on qualifications and relevant pharmacovigilance experience. Shortlisted candidates will be contacted for further evaluation and interview scheduling.

Advance your career in pharmacovigilance operations, safety compliance, and global drug monitoring by applying today.