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ClinChoice

Global CRO providing full-service clinical development

Senior Associate - Aggregate Reporting Physician

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timePasig, Metro Manila, PhilippinesNo salary listedIn-person

About the Job

Requirements

  • Must be a licensed medical physician.
  • Have experience with drug safety, pharmacovigilance concepts, regulatory requirements, research principles, and safety data analysis.
  • Have 1–3 years of experience in pharmaceutical regulations and research and development processes.
  • Be able to analyze, interpret, and present complex data concisely and clearly in oral and written scientific formats.
  • Demonstrate attention to detail, diligence in record keeping and organization, ability to manage a high workload and critical issues, computer literacy, and proficiency in Microsoft Office applications.
  • Have collaborative and interpersonal skills and be able to deliver results independently in a global, cross-functional environment.
  • Be accountable for delivering results.
  • Have decision-making and problem-solving skills.
  • Take a proactive approach and use initiative.
  • Manage, prioritize, plan, and organize work assignments and work under strict timelines.
  • Be able to follow guidelines and working practices.

Responsibilities

  • Help guide report strategy, determine important safety concerns, and review medical and medical safety content for reports, including safety signals, health authority requests, safety-related literature, adverse event case reviews, benefit-risk assessments, and overall medical assessments and conclusions.
  • Collaborate with contributing team members, particularly on reports assigned to the Global Risk Assessment and Safety Physician.
  • Review assigned report stages during the authoring process, record recommended revisions, and indicate completion of reviews in the corresponding systems.
  • Provide medical and scientific judgment in evaluating data about the efficacy and safety of client products, including PBRER-PSURs and benefit-risk evaluations.
  • Contribute to strategy discussions, including determining important safety concerns and reviewing draft and final data, health authority feedback topics, signals, and benefit-risk evaluations.
  • Coordinate with Global Risk Assessment and Safety Physicians regarding PBRER steps and handoffs, and collaborate with other report-authoring team members.
  • Review assigned draft and final reports and provide feedback, including pre-initial, draft, final-draft, and final-report stages.

Desired Qualifications

  • Data entry experience.
  • Experience working with standard operating procedures or work instructions.

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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