Director, Therapeutic Area Lead, Patient Safety Science

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profile Job Location:

Princeton, NJ - USA

profile Monthly Salary: Not Disclosed
Posted on: 7 hours ago
Vacancies: 1 Vacancy

Job Summary

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. 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: Summary

The Patient Safety Science Therapeutic Area Lead will be responsible for leading and managing a team of scientists within a therapeutic area in the Worldwide Patient Safety organization. This critical role involves ensuring the safety of our medicines through effective pharmacovigilance pharmaco-epidemiology and risk management strategies. The role will oversee both pre-marketing and post-marketing product support ensuring compliance with global regulatory requirements and driving strategic initiatives to enhance safety science processes.

Duties & Responsibilities

General Product Scientific Support:

  • Partner with fellow Therapeutic Area (TA) Leads and the Head of Patient Safety Sciences to plan lead and advance programs and talent.

  • Oversee a team of safety scientists and risk management experts globally within the assigned TA.

  • Oversee resources to ensure adequate support to Safety Management Teams (SMTs) for monitoring and managing the emerging safety profile risk identification and risk planning of products.

  • Ensure the availability of analytic support resources for MSA in evaluating the safety profiles of BMS assets.

  • Mentor individuals and teams in aspects of project management SMT requirements core signal detection safety data/Health authority queries and risk management planning.

  • Provide strategic guidance regarding the development and implementation of Global/EU/Local Market Risk Management Plans (RMPs) additional risk minimization measures (aRMM) and additional pharmacovigilance activities (aPVA).

  • Oversee the development maintenance and availability of signal detection and analytic tools and resources.

  • Provide expertise and guidance to teams authoring safety sections/safety deliverables to ensure consistency and compliance with current requirements.

Cross-Functional Activities:

  • Provide subject matter expertise for process improvement and cross-functional initiatives for Safety Science including SOPs and Procedural Documents.

  • Drive interactions with key line functions in support of safety activities between Safety Science and Stakeholders.

  • Establish cultivate and maintain external relationships with key partners within BMS and thought leaders.

  • Represent BMS safety science interests in external groups (regulatory bodies and pharmaceutical industry trade associations).

  • Leadership and Team Development

  • Facilitate skill development by coaching others and sharing expertise.

  • Provide team members with regular and constructive performance feedback.

  • Build a collaborative supportive learning environment and ensure high-quality delivery of pharmacovigilance activities.

  • Ensure timely information is provided to drive accurate decision-making within a designated TA.

Leadership and Team Development:

  • Facilitate skill development by coaching others and sharing expertise.

  • Provide team members with regular and constructive performance feedback.

  • Build a collaborative supportive learning environment and ensure high-quality delivery of pharmacovigilance activities.

  • Ensure timely information is provided to drive accurate decision-making within a designated TA.

Qualifications

  • Health science related degree required. Advanced scientific degree (e.g. PharmD PhD MD) preferred.

  • Minimum of 10 years of relevant pharmaceutical industry experience with significant experience in global pharmaceutical safety risk management.

  • Line management experience is required.

  • Thorough understanding of global pharmacovigilance regulations particularly with respect to DSUR PBRER and Risk Management Planning.

Specific Knowledge Skills Abilities

  • Exemplary leadership skills with proven ability to foster partnerships within a functional area and across organizational boundaries.

  • Effective leadership capability in building high-performance teams particularly across a matrix organization.

  • Demonstrated problem-solving skills including in challenging and ambiguous situations.

  • Creative thinker with exceptional listening and analytical skills.

  • Skilled at being adaptable/flexible and managing multiple demands and shifting priorities.

  • Effective time management and comfortable handling risk and uncertainty.

  • Ability to handle conflict read situations quickly and find common ground for achieving cooperation and resolution.

Travel: This position requires up to 5-10% of travel.

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.

Compensation Overview:

Madison - Giralda - NJ - US: $217520 - $263577 Princeton - NJ - US: $217520 - $263577

The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job such as required skills where the job is performed the employees work schedule job-related knowledge and experience. Final individual compensation will be decided based on demonstrated experience.

Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits please visit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:

  • 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

  • US Exempt Employees: flexible time off (unlimited with manager approval 11 paid national holidays (not applicable to employees in Phoenix AZ Puerto Rico or Rayzebio employees)

  • Phoenix AZ Puerto Rico and Rayzebio Exempt Non-Exempt Hourly Employees: 160 hours annual paid vacation for new hires with manager approval 11 national holidays and 3 optional holidays

Based on eligibility* additional time off for employees may include unlimited paid sick time up to 2 paid volunteer days per year summer hours flexibility leaves of absence for medical personal parental caregiver bereavement and military needs and an annual Global Shutdown between Christmas and New Years Day.

All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.

*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours depending on the nature of their work and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors leased workers and other service providers are not eligible to participate in the program.

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 a supportive culture promoting global participation 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 Protocol

BMS has an 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.

Supporting People with Disabilities

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.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position please visit this page for important additional information: Protection

We will never request payments financial information or social security numbers during our application or recruitment process. Learn more about protecting yourself at data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If you believe that the job posting is missing information required by local law or incorrect in any way please contact BMS at . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.

R: Director Therapeutic Area Lead Patient Safety Science

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Director

Working with UsChallenging. 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 breakthrou...
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Bristol-Myers Squibb is a global biopharmaceutical company focused on discovering, developing and delivering innovative medicines for patients with serious diseases. Our medicines are helping millions of patients around the world in disease areas such as oncology, cardiovascular, immu ... View more

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