Pharmacovigilance Job at Bristol Myers Squibb
Are you passionate about ensuring patient safety and driving innovations in the pharmaceutical industry? Bristol Myers Squibb is seeking a Senior Manager, Patient Safety Scientist in Hyderabad to join their esteemed Patient Safety group. This Pharmacovigilance Job in Hyderabad is integral to maintaining the safety of medicines through advanced pharmacovigilance practices. With a focus on collaboration and excellence, the position offers a unique opportunity to contribute to risk management and regulatory compliance. Dive into a career where your expertise can make a significant impact on patients’ lives globally.
About Bristol Myers Squibb:
Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for patients with serious diseases. The organization is committed to transforming patients’ lives through science and operates in various therapeutic areas, including oncology, immunology, and cardiovascular diseases. With a strong presence in Hyderabad, Bristol Myers Squibb emphasizes a culture of collaboration and excellence in patient safety and pharmacovigilance.
Job Details:
- Location: Hyderabad – TS – IN
- Job Type: Full-time
- Job Requisition ID: R1605042
Job Description:
The Patient Safety group at Bristol Myers Squibb is responsible for ensuring the safety of medicines through comprehensive pharmacovigilance and pharmaco-epidemiology deliverables. This includes monitoring safety, reporting, and contributing to risk management planning and strategy, ensuring compliance with global regulatory requirements. The role of Senior Manager, Patient Safety Scientist is pivotal in executing these responsibilities effectively.
Key Responsibilities:
- Perform core signal detection and assessment activities throughout the product life cycle, demonstrating analytical insight.
- Lead Signal Detection Review Meetings (SDRMs) by evaluating clinical data to support signal detection.
- Execute strategies for signal evaluation and manage signals within the signal management system in this Pharmacovigilance Job in Hyderabad.
- Prepare safety and risk management sections of aggregate safety documents.
- Contribute to the preparation of safety sections in clinical trial documents and represent Patient Safety at meetings at Bristol Myers Squibb.
- Support the safety strategy for regulatory filings and author safety sections of marketing authorization applications.
- Develop and maintain global and local Risk Management Plans (RMPs).
- Collaborate on process improvement initiatives for Patient Safety Science.
Eligibility Criteria for the Pharmacovigilance Job:
- Scientific degree (e.g., BS, MS, RN, PharmD, PhD, MD) or equivalent relevant experience.
- Minimum of 4-6 years of experience in pharmacovigilance or the pharmaceutical industry.
- Understanding of medical concepts and safety activities in drug development.
- Strong analytical and organizational skills with attention to detail.
- Ability to manage timelines and quality of work through effective communication.
- Adaptability to shifting priorities and day-to-day challenges.
- Familiarity with data analysis and emerging technologies.
Required Skills for the Pharmacovigilance Job:
- Solid understanding of pharmacovigilance processes and regulatory requirements.
- Experience in signal detection and risk management.
- Proficiency in writing and reviewing safety documents.
- Strong collaboration and cross-functional partnership skills.
- Ability to leverage automation and innovation tools in daily work.
- Effective communication skills for stakeholder engagement.
- Knowledge of global health authority regulations.
- Commitment to continuous improvement and professional development.
