[Hiring] Senior Manager Safety PV Ops @Bristol Myers Squibb

Role Description

This position provides management role to the oversight of the Global Patient Safety case management, operational oversight of drug safety case management vendor, safety submission compliance, and cross functional collaboration to support risk management and pharmacovigilance activities for the Global Patient Safety department.

Essential Duties/Responsibilities

• Responsible for leading the global ICSR activities to comply with global ICSR regulations.
• Manage and lead the assigned program(s) to support PV operations activities, including study start up preparations up to closure working with various stakeholders.
• Oversee processes, training and compliance of external case management vendors, CAPA development.
• Provide oversight and ensure submission compliance with business partners, CROs and global regulatory authorities.
• Support Inspection Readiness and During Inspection.
• Support general data output/requests for info.
• Ensure data reconciliation of the safety and clinical databases for Serious Adverse Events.
• Effectively utilize metrics to assess productivity, opportunities for workflow and quality improvement, and to measure effectiveness of change initiatives.
• Work with PV management and other cross functional team members to ensure PV compliance and inspection readiness.
• Support data readiness for the production and submission of aggregate reports (e.g., DSUR, and IDMC listings).
• Collaborate with other internal and external functions to ensure alignment among case management, aggregate reporting, and signal detection activities.
• Collaborate with clinical teams in the preparation of and updates to safety-related study documents (e.g., Protocols, ICFs, Safety Management Plans, PVA or SDEA, DMP, ECCG plan, SAE Recon Plan, DTA Plan, Monthly Data Review, etc.).
• Collaborate with the Quality Management function to develop or update Standard Operating Procedures and Work Instructions for PV and Safety, which are integrated and fully aligned.
• Significant cross-departmental interactions with other RayzeBio functions, including Clinical Data Management, Clinical Operations, Clinical Development, and Quality Assurance groups.

Supervisory Responsibilities

• Interactions with internal/external cross functional Team members.

Qualifications

• BS/BA degree in related discipline and a minimum of 10 years of related experience; or, equivalent combination of education and experience.
• Drug Safety and Pharmacovigilance including at least 8+ years of experience in Pharmacovigilance Operations.
• Working knowledge of and experience with international regulatory Adverse Event Reporting requirements.
• Proven experience and effectiveness at guiding PV vendor staff.

Knowledge, Skills and Abilities

• Extensive knowledge of biotechnology/pharmaceutical sector drivers and practices.
• Demonstrates excellent knowledge of relevant US and international regulations, guidance and initiatives governing both clinical trial and post-marketing safety environments.
• Demonstrates advanced skill and keen insight in gathering, sorting and applying key information to solve problems.
• Demonstrates strong organizational and planning capabilities by managing time, workload, and resources of a function.
• Leads and manages a functional area within a department to execute on team functional objectives that contribute to accomplishing common functional and departmental goals.
• Demonstrates high standards of verbal and written communication. Provides timely and appropriate information updates.
• Fosters collaboration among team members. Encourages teams to align on common goals.
• Strong interpersonal skills and skilled at effectively resolving challenges by developing an agreed upon resolution.
• Develops procedures, tasks, and tools.
• Trains and mentors staff on departmental products, tools, and data sources.
• Capable of proactively assessing workload, trends, tasks, and priorities for cross-functional activity.
• Plans and executes multiple projects or activities, considering alternative methods and contingency plans to avoid potential issues.
• Designs and implements solutions to address cross functional project level challenges, taking into consideration the broader impact.
• Engages, influences, and collaborates with stakeholders on cross-functional projects.
• Applies AI to improve team execution and decision-making.

Work Environment/Physical Demands

• FT/On site and/or Remote work.

Compensation Overview

• Princeton - NJ - US: $149,860 - $181,595.
• San Diego - CA - US: $164,846 - $199,754.
• The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis.

Benefits

• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
• Work-life benefits include Paid Time Off.
• Eligibility for specific benefits listed on our careers site may vary based on the job and location.