- Full Time
- Hyderabad - TS
Website Bristol Myers Squibb
Table of Contents
ToggleAbout Bristol Myers Squibb
Bristol Myers Squibb acknowledges the importance of maintaining a balance and flexibility in our work environment. We provide a wide array of competitive benefits, services, and programs that equip our employees with the resources they need to achieve their goals both professionally and personally. BMS Hyderabad serves as an integrated global hub, dedicated to helping patients overcome serious diseases by developing sustainable and innovative solutions. This crucial center for science, technology, and innovation supports a variety of technological and drug development activities, driving the next wave of advancements.
Post: Pharmacovigilance Associate
Job Description
Position Responsibilities
Signal Detection/Safety Data Review
- Signal Detection Support
- Generate and file data for signal detection and safety data review.
- Execute literature searches and retrieve full-text articles.
- Support Safety Data Review Meetings (SDRMs) and manage logistics.
Signal Documentation and Notifications
- Generate reports and upload into Signal Tracker.
- Conduct Quality Checks (QC).
Safety Management Team
- Create and manage SMT Membership List, Mail Group, and File Share.
- Set up and maintain associate systems (Sharepoint, Document Management System).
- Schedule routine meetings and manage asset closeouts.
- Administer MSAPSMT mailbox and meeting calendar.
- Manage access, permissions, and content for SMT OneSafe and SharePoint Online.
Scheduled Aggregate Report
- Obtain exposure data and update documents.
- Generate and file supporting data.
- Support literature searches for full-text articles.
Document Compliance, Management, Support
- Transfer data into reports.
- Format documents.
- Follow up on queries.
- File, track, and close documents.
Other Activities
- Manage data received in PV mailbox.
- Update signal detection lists related to MedDRA upgrades.
Candidate Profile
- Education: BS/RN/MS/PharmD in life sciences or equivalent.
- Experience: Minimum of 2 years in health sciences, life sciences, medical fields, pharmaceutical industry, or academia.
- Skills: Understanding of global pharmaceutical drug development lifecycles.
- Preferred Qualifications:
- Proficiency in pharmacovigilance processes.
- Experience in data organization, coordination, and communication.
- Project or program management experience.
Key Competency Requirements
- Understanding of pharmacovigilance activities/processes and medical concepts.
- Ability to manage timelines and work quality using organizational and interpersonal communication skills.
- Collaborative and communicative with attention to detail, scientific, analytical, and conceptual skills.
Operational Skills
- Technical Proficiency: Basic operational software and automation tools.
- Process Management: Ability to evaluate and suggest digital improvements.
- Problem-Solving: Addressing problems with digital solutions.
Analytical Skills
- Data Management: Processing and recording data in structured formats.
- Critical Thinking: Identifying flaws and inconsistencies in data or processes.
- Data Analysis: Basic data gathering and reporting using standard tools.
Additional Information
- Experience: Minimum 2 years.
- Qualification: Bachelor of Science in life sciences or equivalent.
- Location: Hyderabad, Telangana.
- Industry Type: Pharma/Healthcare/Clinical Research.
- Functional Area: Pharmacovigilance.
- End Date: 25th July 2024
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