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Associate Director, Scientific Content Development, Congress Engagement

Associate Director, Scientific Content Development, Congress Engagement

MediabistroBlawenburg, NJ, United States
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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. 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 .

The Associate Director, Scientific Content Development, Congress Engagement is responsible for the planning, management, and support of medical content and experiences at key congresses. This person reports to the Director, Congress Strategy Lead and works closely with Medical Affairs teams across therapeutic areas to build the medical congress strategy based on medical priorities. The Scientific Content Development Lead also supports the planning process that aligns medical priorities and defines medical booth content for key congresses. This role requires strong project management and communication skills.

Key Responsibilities

Responsible to support the creation of an overarching booth story by integrating various elements and ensuring that the content aligns with the strategic objectives of the therapeutic area

Support innovation, idea generation and execution of objectives to continually evolve processes and enhance the value of congress engagement.

Coordinate strategic input gathering and engaging with internal teams including Congress Engagement Team, Portfolio Strategy, Early Assets group, and franchise leads to align on booth communication objectives, prioritizing assets for congress

Strategic input gathering for congress booth content planning. This includes the review of externally published and BMS internal resources to understand the company's priorities, overarching timelines and asset positioning.

Conduct strategic level discussions with senior Medical Leadership and multiple disease asset teams to determine overall booth communication objectives.

Manage the Medical Legal Review (MLR) process for congress both theme and content globally.

Create overarching congress booth story in alignment with BMS and local market guidelines.

Manage agency partners to ensure deliverables are met within budget and timeline.

Utilize platforms such as Veeva for content creation, management, and distribution to ensure consistency and compliance.

Content and ensure a feedback loop to association congress organizers to secure approvals where needed.

Responsible for ensuring BMS improves congress effectiveness and efficiency while also driving innovative solutions for improving the overall customer experience at Congresses.

Partner with congress leads to deliver scalable, innovative solutions across therapeutic areas, and share best practices to enhance congress planning and execution.

Working efficiently within an assigned budget, leveraging emerging technologies to drive efficiencies. o Attend congresses and provide input on creation of executive summary around competitive activities and data from medical booth (i.e., downloads, visits.)

Model BMS behaviors and reinforces such behaviors at all levels in the organization.

Qualifications & Experience

Minimum of seven years' congress management experience or relevant experience in pharmaceutical marketing and / or medical affairs preferred.

Experience in change leadership and demonstrated success in leading across a cross-functional matrix team. Excellent organizational, written and oral communication, facilitation, interpersonal and leadership skills.

Track record of success in leading complex projects. Demonstrated strong project management skills; Project Management Certification (PMP) a plus.

Expert experience in managing 3rd party vendors and contracts.

Proven strength at communicating effectively across a global audience.

Knowledge of the Medical Legal Review process, including associated systems (Veeva Vault PromoMats)

Demonstrate innovative mindset (simplification - doing things better, faster and more cost effectively).

Knowledge of international healthcare customers, stakeholders and influencers and understanding of their needs.

Ability to flex across different types of cultures, complexities, business situations and matrix partners.

Problem solver and results oriented.

Proven experience in managing timelines, identifying resource needs and constraints, and implementing strategies to meet changing needs and requirements.

Knowledge of industry trends and experience in leading and driving operational programs and initiatives.

Ability to travel 20%-35% to attend key domestic and international congresses

#LI-Hybrid

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.

Compensation Overview :

Madison - Giralda - NJ - US : $155,540 - $188,480

Princeton - NJ - US : $155,540 - $188,480

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 employee's 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 https : / / careers.bms.com / life-at-bms / .

Benefit offerings are subject to the terms and conditions of the applicable plans then in effect and may include the following : Medical, pharmacy, dental and vision care. Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources and a 401(K). Financial protection benefits such as short- and long-term disability, life insurance, supplemental health insurance, business travel protection and survivor support. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. Parental, caregiver, bereavement, and military leave. Family care services such as adoption and surrogacy reimbursement, fertility / infertility benefits, support for traveling mothers, and child, elder and pet care resources. Other perks like tuition reimbursement and a recognition 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.

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.

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 : https : / / careers.bms.com / california-residents /

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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Scientific Director • Blawenburg, NJ, United States

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