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ClinChoice

Global CRO providing full-service clinical development

Area/Local Safety Officer Consultant

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBrazilNo salary listedIn-person

About the Job

Requirements

  • Health care science professional or equivalent training.
  • Significant training in data management and strong information technology skills.
  • Two to four years of relevant experience, such as case data management, reconciliation management, or vigilance IT project management.
  • Fluency in English and French as a mother tongue.
  • Ability to work independently and establish a high-trust environment with client counterparts.
  • Excellent communication skills and ability to work with cross-functional teams.
  • Rigor.

Responsibilities

  • Perform quality checks of pharmacovigilance cases and ensure English translations are properly completed.
  • Maintain a local tracker of individual safety reports.
  • Serve as the local subject matter expert for case management activities.
  • Monitor regulatory submission timelines for safety reports and communicate potential delays to appropriate teams.
  • Establish and maintain local indicators for safety-report submission compliance.
  • Oversee training for local employees and business partners, maintain key performance indicators, and present them during regular team meetings.
  • Monitor regulatory changes affecting vigilance activities and responsibilities.
  • Reconcile information with distributors, third parties, vendors, and internal stakeholders.
  • Oversee proper identification of local literature articles for adverse-event reporting as required.
  • Submit safety reports, updates, and information—including serious adverse events, special situations, suspected unexpected serious adverse reactions, periodic safety update reports, and risk management plans—to local health authorities and other client departments as applicable.
  • Support the Area Safety Lead in notifying local health authorities of safety issues, including significant safety issues, emerging safety issues, and signals.
  • Maintain current knowledge of local pharmacovigilance, cosmetic vigilance, and device vigilance requirements, including reporting requirements for applicable product classes in the territory, and collaborate with the global team to implement process changes for newly identified requirements.
  • Record self-identified non-conformances and collaborate with the global team to investigate them and develop and implement effective corrective and preventive actions.
  • Perform other agreed tasks assigned by the manager.
  • Manage and archive documents as required.
  • Maintain current knowledge of relevant company procedures and training.
  • Develop, update, and implement local procedures to ensure compliance with client global procedures and national requirements.
  • Support local health authority inspections and audits, respond to queries during inspections, and collaborate with the global team to develop and implement corrective and preventive action plans as applicable.
  • Provide pharmacovigilance clauses for local agreements and contribute contract-related information to the pharmacovigilance system master file.
  • Ensure implementation of local business continuity plans, including inspection readiness and adverse-event reporting coverage.

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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