Sorry, this listing is no longer accepting applications. Don’t worry, we have more awesome opportunities and internships for you.

Intern, Worldwide Medical Affairs – Myeloid (Summer 2023)

Bristol Myers Squibb

Bristol Myers Squibb

Intern, Worldwide Medical Affairs – Myeloid (Summer 2023)

Summit, NJ
Full Time
Paid
  • Responsibilities

    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

    Position Summary

    He/she will provide scientific/medical support for compounds in stage of clinical development and participate in a Q1/Q2 Global product launch and/or post-launch activities.  This individual will support the implementation of a strategic disease area medical plans, and integrated evidence planning, working cross functionally, with development, marketing and market access. They will also support data analysis, publication and clinical study needs. In addition, they will assist in the evaluation and support of investigator-initiated trials and support Global Medical Affairs (GMA) Advisory Boards. They will also support compassionate use or related patient access programs as directed within GMA-Myeloid.

    Key Responsibilities

    • Supporting responsibilities: Strategic and Tactical

      • Collaborate with all Regional Disease representatives and functional teams in Medical Affairs on Disease strategy and tactics ensure integrated evidence plans are current

      • Support Medical affairs cross-functional sub team meetings

      • Support in the execution of Global advisory boards and steering committee meetings, but also be involved in assisting the regions on critical globally impactful advisory boards

      • Perform, as needed, research and analytics and provide recommendations to support quality medical decisions regarding clinical research, consultancy, and internal planning

      • Conduct research and provide directed analytics and valuable backgrounders, as well as provide recommendations to guide Medical Leadership Investigator Initiated Trials (IITs) decisions

    • Deliverable responsibilities:  Strategic and Tactical

      • Assist with Global Franchise Disease Strategy and Plans

      • Track and coordinate with Regional & Affiliate Medical Affairs tactics in Disease Plans

      • Partner with Scientific Communications on developing Disease publication strategy, gap analysis, key messages in coordination with the Regions

      • High quality scientific/clinical input and review of (as needed):

      • Disease strategy/plans

      • Abstracts, posters, slides, manuscripts in disease area

      • Educational materials in disease area including slides, webcasts, etc

      • Key Opinion Leader (KOL) Steering committee meeting objectives, materials

      • Open Research Questions process, and integrated evidence planning in disease area

      • Assist with scientific searches, data summaries, preparation for site visits/corporate visits/payor presentations

    • Actively engage/interact with key stakeholders, including:

      • Med Affairs partners in disease area

      • Global Medical Affairs Leadership

      • Marketing

      • Market Access

      • Clinical Research & Development

      • Biostatistics

      • Translational Development

      • Regulatory Affairs

      • Project Leadership

    Qualifications & Experience

    • Students obtaining an undergraduate or advanced degree (BS, MS, Pharm D, PhD or others) in molecular biology, genomics, cancer biology or other relevant life sciences area

    • Strong organizational skills

    • Excellent oral and written communication skills

    • Hard working with a can-do attitude

    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

    Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

    COVID-19 INFORMATION

    To protect the safety of our workforce, customers, patients and communities, the policy of the Company requires all employees and workers in the U.S. and Puerto Rico to be fully vaccinated against COVID-19, unless they have received an exception based on an approved request for a medical or religious reasonable accommodation. Therefore, all BMS applicants seeking a role located in the U.S. and Puerto Rico must confirm that they have already received or are willing to receive the full COVID-19 vaccination by their start date as a qualification of the role and condition of employment. This requirement is subject to state and local law restrictions and may not be applicable to employees working in certain jurisdictions such as Montana. This requirement is also subject to discussions with collective bargaining representatives in the U.S.

    BMS is dedicated to ensuring that people with disabilities can perform complex functions through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an accommodation prior to accepting a job offer. If you require reasonable accommodation 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 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.

  • Industry
    Pharmaceuticals
  • About Us

    Bristol Myers Squibb is a leading global biopharma company focused on discovering, developing and delivering innovative medicines for patients with serious diseases in areas including oncology, hematology, immunology, cardiovascular, fibrosis and neuroscience. Our employees work every day to transform patients’ lives through science.