Associate Director Scientific Publications- Oncology

Profile

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis.

Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results.

Department: WW Scientific Publications

Location: Princeton Pike (Lawrence Township, NJ)

Description:

The Worldwide Scientific Publications organization’s mission is to support the development of high quality medical publications to ensure clear, scientific communication of BMS data enabling the safe, appropriate use of and access to BMS medicines. The primary responsibility for the Scientific Publications Associate Director, Oncology is to development and deliver comprehensive, globally-aligned strategic publication plans and lead the execution of publications to enable the disclosure of evolving BMS data.

Qualifications:


Advanced degree: PharmD, PhD or equivalent in a science subject or biomedical subject preferred;

Oncology experience strongly preferred

3 years in medical writing and relevant industry work experience; experience in medical communications

Working knowledge of scientific publication strategy, planning and execution during all phases of drug development and commercialization process

Understanding of good publication practices and guidance (GPP3, ICMJE), Sunshine Act, Pharma Code of Conduct, and other guidance related to post-marketing practices and scientific data communication

Understanding of clinical trial design and execution, statistical methods and clinical trial data reporting requirements

Ability to analyze and interpret complex clinical information

Experience working in highly matrix environment across a broad range of functional areas

Attention to detail, excellent editorial skills, and familiarity with the AMA style guide

Excellent organizational skills

Strong management and leadership skills

Ability to travel domestically and internationally approximately 15-20% of the time


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 the resources to pursue their goals, both at work and in their personal lives.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Company info

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