Bristol - Myers Squibb is a differentiated company, led by our unique BioPharma strategy that leverages the reach and resources of a major pharma company paired with the entrepreneurial spirit and agility of a biotech firm. We work every day to deliver innovative medicines for patients with serious and life-threatening diseases. Each day, our employees around the world work together for patients – it drives everything we do. We are focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Through our R&D organization, we have built a sustainable pipeline of potential therapies, and actively partner to access external innovation to broaden and accelerate our work.
Post : Pharmacovigilance (PV) Associate
Job Description
• The incumbent has a key role in tracking and following up on actions and responses of experts and and other stakeholders, ensuring that timelines, resources and information are coordinated and and documented accurately and in a timely manner.
• Medical Safety Assessment Physicians, Medical Survelliance Teams, Safety Data Review Teams
• Supports Medical Safety Assessment Physicians (MSAP) in leading and coordinating individual cross-functional Medical Surveillance Teams (MSTs) and assigned sub-teams, such as Safety Data Review (SDR) Teams.
• Creates meeting agendas for MST and assigned sub-teams, and documents of decisions, conclusions, timelines, milestones and action items in team minutes.
• Identifies post-meeting actions, and ensures responsibilitites and timelines are assigned and met.
• Assesses and appropriately elevates issues impacting key MST activities, milestones, documents to the appropriate Global Pharmacovigilance & Epidemiology (GPV&E) colleagues.
• Leads, plans, organizes, and forecasts requirements and/or resources based on Book of Work and other upcoming tasks and activities for assigned product portfolio.
• Executes searches of the corporate safety database, J-review database and the worldwide literature, applying critical thinking and independent research skills to ensure the information is appropriate and usable.
• Applies medical, life science and general scientific knowledge and expertise to create and manage plans and budgets for designated projects.
Candidate Profile
• Bachelor of Science in life sciences or equivalent relevant scientific qualifications or professional training.
• Minimum of 2 years' professional experience in health science or relevant life sciences/medical fields, or appropriate pharmaceutical industry or academic experience.
• Demonstrated understanding of global pharmaceutical drug development and drug lifecycles.
• Demonstrated excellence in scientific technical skills with a comprehensive understanding of pharmacovigilance processes.
• Extensive experience in the analysis and communication of data and information to key stakeholders.
• Project or program management experience and/or qualifications
• Experience in working with committees and diverse teams
Additional Information:
Experience : 2 years
Qualification : Bachelor of Science in life sciences
Location : Tampa - USA
Industry Type: Pharma
Functional Area : Pharmacovigilance
End Date : 10th May, 2018
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