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Associate Director, Strategy and Operations – WW Hematology Medical
$121k-147k (estimate)
Full Time | Pharmaceutical 3 Weeks Ago
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Bristol-Myers Squibb is Hiring an Associate Director, Strategy and Operations – WW Hematology Medical Near Lawrence, NJ

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t 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. You’ll 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: careers.bms.com/working-with-us.

Global Medical Affairs, Strategy and Operations is responsible for the global planning activities of the Hematology Medical Affairs Department, including global/regional brand and medical planning, budget planning, congress planning, workforce planning, and planning and execution of special projects. The Associate Director, Strategy and Operations is responsible for partnering with colleagues in Medical Affairs and in other functions including Commercial, both Heme and Cell Therapy to lead or support Strategic Planning responsibilities.

Responsibilities will include, but are not limited to, the following:

  • Responsible for coordinating the various Medical Affairs functions involved in the global brand, launch and medical affairs plans to develop and communicate effectively the Medical view in the global medical and marketing planning process.
  • Responsible in setting agendas for key WW Hematology Medical meetings. Team Meetings, Town Halls
  • Responsible for working with the WW Hematology Medical Teams as well as Cross-Functional Partners and coordinating the Integrated Evidence Plans (IEPs) for each disease area for life cycle management in collaboration with key cross-functional stakeholders, as well as supporting the Medical Planning Process
  • Working with Medical Affairs IT to evaluate hardware and software packages for WW and US Medical Affairs, evaluating the budget impact, compatibility with existing systems, resource needs for implementation.
  • Collaborating with Medical Evidence Generation Teams, the other WW Hematology and Cell Therapy Medical and Commercial S & Ops Teams, GDO and GDD Teams
  • Responsible for coordinating TL engagements for President, CTO and CTLT members at Tier 1 priority global congresses as needed. This include having oversight of which CTLT members (across Medical, Commercial, Research, Development and Manufacturing) are attending which congresses, which TLs they should meet and objectives for each
  • Establishing departmental workforce plans across Global Medical Affairs departments
  • In collaboration with Finance, establish budgets for WW Hematology Medical Affairs (IIT budgets for all regions, including US, EU, Asia Pacific). Work within Medical Affairs and Finance to forecast IIT cost recognition and develop risk-adjustment model to allow better forecasting of committed spending.
  • Track against workforce plans and budget performance against plans monthly
  • Develop with Medical Affairs Excellence dashboards for deliverables and communicate appropriately on a regular basis; Working with BI&A to develop regular monthly reports
  • Collaborate with Scientific Communications and Global Franchise Teams to ensure asset teams complete publication plans for all disease areas, and to update them regularly
  • Work with Scientific Communications to track abstracts and publications against the plans
  • Work with other key stakeholders in regions to identify best practices of all Medical Affairs Functions, evaluate skills, competencies and capabilities in the groups, and identify areas that can be improved
  • Responsible for special projects that require Medical Leadership and involve cross-functional teams.
  • Working with other PMs on the team, ensuring consistent communication, tracking of congress activities, budgets, and other medical activities such as impact agenda, etc.

Skills/Knowledge Required:

  • BS/BA required; 5 years of experience in industry required, experience in industry, or research in the pharmaceutical/biotechnology industry or academics preferred. Experience in clinical research and development, or medical affairs in Hematology/Oncology preferred
  • Operational experience across a range of commercial and/or R&D roles a plus
  • Must demonstrate ability to lead strategically, drive performance, build alignment, inform, negotiate and collaborate.
  • Effective communication skills – written, oral, and interpersonal.; experience in delivering complex messages to various internal and external customers with a track record of effective and influential presentations.
  • Proven track record in matrix functions exerting influence to achieve results rather than counting on organizational authority
  • Demonstrates initiative, creativity, strategic capabilities, and ability to work effectively in complex, rapidly changing environments
  • Proven team player with ability to navigate cross functionally
  • Experience in designing and tracking Key Performance Indicators preferred
  • Demonstrated experience in developing & implementing state of the art medical planning processes in a multi-national environment.
  • Proven ability to acquire & manage multiple therapeutic area expertise –International experience highly desirable.

Strong technical skills, including advanced Excel, SharePoint, TEAMS and other analytics & business intelligence and finance (Tableau, Ariba/SAP, SharePoint, Workday, Room scheduler experience strongly desired.

Compass, etc.) software

If you come across a role that intrigues you but doesn’t 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 Protocol

BMS 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 adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility 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.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Pharmaceutical

SALARY

$121k-147k (estimate)

POST DATE

06/07/2024

EXPIRATION DATE

06/10/2024

WEBSITE

bms.com

HEADQUARTERS

NEW YORK, NY

SIZE

15,000 - 50,000

FOUNDED

1858

TYPE

Public

CEO

GIOVANNI CAFORIO

REVENUE

$10B - $50B

INDUSTRY

Pharmaceutical

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About Bristol-Myers Squibb

Bristol-Myers Squibb is a biopharmaceutical firm that discovers, develops and delivers medicines for patients prevail over serious diseases.

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