Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation.
Post : Pharmacovigilance Associate
Job Description
Position Responsibilities
Apply medical, life science and general scientific knowledge and expertise to effectively support the following :
Signal Detection/Safety Data Review
Signal Detection Support
• Generate and file data for signal detection and safety data review
• Execute literature searches and retrieve and deliver full-text articles
• Safety Data Review Meeting (SDRMs) support and logistics
Signal Documentation and Notifications
• Generates reports and upload into Signal Tracker
• Quality Check (QC)
Safety Management Team
• Create and manage SMT Membership List
• Create and manage SMT Mail Group
• Create and manage SMT File Share (i.e., Safety Data Review Folder)
• Create and manage associate systems (i.e., Sharepoint [SP] site, Document Management System)
• Schedule routine meetings
• Manage asset close out
• Manage MSAPSMT mailbox/meeting calendar
• Manage access, permissions and content related to SMT OneSafe and SharePoint Online for assigned assets.
Scheduled Aggregate Report
• Obtain Exposure data and update document
• Generate and file supporting data
• Support literature searches and deliver full-text articles
Document Compliance, Management, Support
• Transferring data into reports
• Formatting
• Querying follow up
• Closing, filing, tracking
Other Activities
• Manage data received in PV mailbox
• Update signal detection lists (e.g., Monitored events, Literature search terms, etc.) related MedDRA upgrades
Candidate Profile
• BS/RN/MS/PharmD in life sciences or equivalent relevant scientific qualifications or professional training.
• 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 lifecycles.
Ideal Candidates Would Also Have :
• Demonstrated excellence in scientific technical skills with a comprehensive understanding of pharmacovigilance processes.
• Extensive experience in the organization, coordination, and communication of data and information.
• Project or program management experience and/or qualifications.
• Experience in working with diverse teams.
Key Competency Requirements
• Working understanding of pharmacovigilance activities/processes and medical concepts.
• Working understanding of team priorities and milestones.
• Ability to manage timelines and quality of work using organizational and interpersonal communication skills.
• Good collaborative and communication skills.
• Attention to detail with scientific, analytical and conceptual skills and the ability to reach reasoned conclusions.
Operational Skills :
• Technical Proficiency: Basic use of standard operational software and tools for automation.
• Process Management: Understanding of current processes and ability to evaluate and suggest digital improvements.
• Problem-Solving: Addresses straightforward problems with simple digital solutions.
Analytical Skills :
• Data Management: Processes and records data and information in structured computer readable formats
• Critical Thinking: Identifies flaws and inconsistencies in data or business processes by considering the system wide impact
• Data Analysis: Can perform basic data gathering and reporting using standard tools.
Additional Information
Experience : Minimum of 2 years
Qualification : Bachelor of Science in life sciences or equivalent
Location : Hyderabad - TS
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Pharmacovigilance
End Date : 25th July 2024
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