Job Description

Working with Us
Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.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. Read more: .Functional Area DescriptionThe Worldwide Patient Safety group is responsible for ensuring the safety of our medicines. This includes all pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy, and execution of certain post-marketing commitments and ensuring compliance with global regulatory requirements.Position Summary / ObjectiveSupport case processing of SUSARs/expedited safety reports in BMS Safety Database. Closely work with Safety Scientists and Medical Review Safety Physicians within in WorldWide Patient Safety (WWPS) in expediting the processing of SUSAR casesPosition Responsibilities

• Perform high quality data entry of Individual Case Safety Reports/SUSARs within corporate safety database including patient/study information, product details and perform MedDRA coding of events, laboratory tests and all required data fields for case completeness.
• Complete and enter high-quality narrative for expedited safety reports to ensure all safety information is accurate, integrated and current, and is submitted within regulatory timelines.
• Participate in the evaluation of serious adverse event reports from spontaneous reports, clinical trials, non-clinical reports and scientific literature as needed.
• Assist in review of new follow-up information and summarize information required MRSP triage assessment of follow-up information.
• Review and QC all forms and documents pertaining to a case for errors, missing information.
• Identify additional information required from clinical database and collaborate with MRSP to prepare queries to obtain additional information.
• Generate reports from corporate safety database to prepare contextual summaries/Analysis of Similar Events as required for expedited safety reports and for other requirements.
• Coordinate all activities around the preparation, evaluation, review and submission of expedited safety reports.
• Attach appropriate queries for missing/discrepant information and add follow-up letters as per WWPS standard operating procedures and work instructions.
• Consult MRSP and Expedited Safety Reporting (ESR) team, whenever there are queries related to SUSAR processing.
• Assist in reporting of SUSARs/ESRs to Investigators and other stake holders by coordinating with clinical operations and submissions team as required.
• Responsible for escalating the issues or tasks outside the normal scope of work.

(Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned)(Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned)Degree RequirementsBSc/MSc Nursing; B. Pharm/M.Pharm/Pharm.D/BDS/BPT/ MPT or Healthcare Degree preferred.Experience Requirements1-2 years of Drug Safety or clinical experience within the pharmaceutical industry is preferred.Key Competency Requirements

• Ability to apply medical, scientific and clinical knowledge in reviewing safety-related documents (relevant source documents) and incorporating key concepts to clearly present the reported events, and in turn, maintain patient safety.
• Experience working in a post-marketing safety or clinical trial setting (i.e., CRO, pharmaceutical company and academic setting).
• Experience working in teams, including supporting other team members when necessary.
• Strong prioritization skills to ensure that processes, procedures and best practices are consistent across WWPS; and that all applicable regulatory requirements are met in a timely manner with high quality.
• Ability to make constructive recommendations to improve processes.
• Demonstrates the ability to multi-task, and flexibility to meet changing business priorities.
• Ability to collaborate within multi-disciplinary team on drug safety-related issues including informing safety physicians and scientists within the therapeutic area on case-related issues.
• Ability to apply sound analytical thinking and database query skills to gather, review, summarize and evaluate critical information in a timely manner.
• Ability to support WWPS Vision and Mission through an understanding of the impact and implications of daily work on all customers of the Expedited Safety Reporting team.

If you come across a role that intrigues you but doesnt perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Bristol-Myers Squibb