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ClinChoice

Global CRO providing full-service clinical development

Senior Associate - Medical Review Physician

Medical, Clinical & VeterinaryConfirmed live in the last 24 hours
Full-timePasig, Metro Manila, PhilippinesNo salary listedIn-person

About the Job

Requirements

  • At least 2 years of experience as a medical reviewer for Individual Case Safety Reports (ICSRs).
  • Thorough knowledge of International Council for Harmonisation Good Clinical Practice (ICH-GCP), relevant Good Pharmacovigilance Practices (GVP) modules, 21 CFR guidelines, and other regulatory requirements.
  • Training and mentoring skills related to GVP concepts and medical aspects, including disease conditions and product portfolios.
  • Hands-on experience with Microsoft Office applications, including Outlook, Excel, Word, and PowerPoint.

Responsibilities

  • Understand relevant Good Pharmacovigilance Practices (GVP) modules.
  • Perform medical review of non-serious and serious Individual Case Safety Reports (ICSRs), emphasizing seriousness, expectedness, causality, and narrative quality while maintaining compliance.
  • Conduct medical review of ICSRs received from spontaneous reports, literature, regulatory authorities, solicited sources, and clinical trials.
  • Support case triage and determine seriousness and relatedness across assigned products.
  • Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) codes, assess labeling, and review narratives.
  • Acquire and maintain current knowledge of the product portfolio and safety profiles across therapeutic areas.
  • Participate in process improvement activities, including implementation of quality control processes.
  • Provide medical guidance and expert opinions on cases to data entry associates and quality reviewers to help resolve queries.
  • Identify and resolve case issues, coordinate with client therapeutic teams and the functional team, and manage issues as appropriate.
  • Maintain pharmacovigilance expertise and understanding of international safety regulations and guidelines.
  • Complete medical review activities in the safety database within stipulated service-level agreements and regulatory timelines.
  • Provide timely feedback to case processors on errors and discrepancies.
  • Assist with training and mentoring case processing and medical review personnel as needed.
  • Adapt to different client case-processing conventions and multitask according to business needs.
  • Perform ad hoc tasks assigned by the team lead or manager while maintaining quality and compliance with project requirements.
  • Participate in organizational activities that meet objectives appropriate to the role and area of expertise.

About the Company

ClinChoice

Global CRO providing full-service clinical development

ClinChoice is a global contract research organization (CRO) that provides outsourced clinical development services across the full lifecycle for pharmaceutical, biotechnology, medical device, and consumer health customers. It delivers services such as clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance to support trials from early development through post-approval. The company differentiates itself with a large, global workforce—over 4,000 professionals in more than 30 countries—and growth through mergers and acquisitions, enabling multinational trial execution. Its goal is to help clients accelerate approvals and navigate complex regulatory environments by offering flexible project-based and FSP engagement models for end-to-end development and lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Whitemarsh Township, Pennsylvania
Founded
1995

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