Directeur(rice) de comptes pour TELUS PME, expert en développement de relations et vente. Acquérir de nouveaux comptes et gérer le cycle complet des ventes.
About the role
- Associate Medical Safety Director managing Medical Safety activities and providing pharmacovigilance expertise for IQVIA. Collaborating with teams in evaluating drug safety and regulatory compliance.
Responsibilities
- Participating in all aspects of the Medical Safety activities as per scope of work
- Providing and maintaining of PV and risk management expertise to internal and external stakeholders
- Maintaining knowledge relevant to allocated product portfolios
- Conducting medical evaluation of post-marketing adverse drug reactions
- Review and contribution to signal management and benefit-risk evaluation of drugs in clinical trial and post marketing
- Preparation, and/or contribution to responses to questions from health authorities
- Reviewing and contributing to periodic aggregate reports
- Contributing to safety review of study protocols, investigators brochure and other reference safety information
- Serving as an internal consultant for any medical support for pharmacovigilance operations
- Providing aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile
- Leads signal detection and analysis
- Providing medical review and contribution to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports
- Providing medical review and contribution to Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
- Review and contribute to benefit-risk evaluation of drugs in clinical trial and post marketing set up
- Providing safety oversight and contribution for label development, review, and updates
- Performing medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs)
- Representing safety and clinical data review findings during internal and external stakeholder meetings
- Providing medical safety support, contribution, and attendance at Safety Governance and other Meetings as needed
Requirements
- A medical degree from an accredited and internationally recognized medical school
- Around three years of clinical practice experience with two additional years in the pharmaceutical or associated industry, or equivalent combination of education, training and required experience
- Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice and clinical trials and pharmaceutical research process
- Maintain knowledge of assigned product portfolio, therapeutic area, and recent literature
- Experience in Signal detection, Aggregate reports and Risk management.
- Capability to synthesize and critically analyze data from multiple sources and communicate complex clinical issues and analyses orally and in writing
- Ability to establish and meet priorities, deadlines, and objectives
- Demonstrated skills in contributing to multiple assignments required, capacity to work under pressure as well as initiative and flexibility and ability to adapt to changing business needs
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients, including mentorship if needed.
Benefits
- Health insurance
- Professional development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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