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ClinChoice

Global CRO providing full-service clinical development

Safety Surveillance Physician

Physicians & SurgeonsPosted on Nov 10
Full-timePasig, Metro Manila, PhilippinesNo salary listedIn-person

About the Job

Requirements

  • Must be a board-certified medical physician.
  • Knowledge of pharmacovigilance concepts, regulatory requirements, research principles, and safety data analysis is required.
  • At least one year of clinical experience or experience in pharmaceutical medicine is required.
  • Ability to analyze, interpret, and present complex data clearly in oral and written scientific formats is required.
  • Proficiency in Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook, with document formatting, data analysis, and presentation capabilities is required.
  • A Bachelor's degree in any medical allied course is required.

Responsibilities

  • Perform alert triage within predefined timelines by systematically reviewing cases and aggregate data in safety databases and reviewing trends to identify potential safety signals.
  • Validate signals and support signal evaluation by reviewing, analyzing, interpreting, and summarizing case and aggregate safety data from clinical, post-marketing, observational study, medical literature, health authority, and product quality sources.
  • Assist in developing and implementing post-marketing data surveillance strategies and product-specific medical safety approaches.
  • Participate as a member of matrix teams addressing product-specific safety.
  • Support evaluation of novel and computer-assisted tools and methodologies for analyzing safety data.
  • Track signal disposition and signal management activities in relevant tracking systems.
  • Support maintenance of documentation relevant to signal detection and management activities.

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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