Director, Regulatory Medical Writing, Oncology F409

Director, Regulatory Medical Writing, OncologyAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured. We are recruiting for a Director to join the Regulatory Medical Writing team to support the Oncology therapeutic area.Position SummaryThis position is accountable for setting the strategy and operational execution for the Prostate/Solid Tumor Targeted Therapy portfolio within the Oncology Regulatory Medical Writing team. Recognized expert medical writer for any documents within and across therapeutic areas. Partners in close collaboration with leadership across GD, the TAs, and the overall R&D organization to provide high quality deliverables successfully and efficiently.Principal ResponsibilitiesWorks closely with key functional stakeholders in the Oncology TA and Delivery Unit to drive RegMW strategy and tactics.Oversees adequate resource planning, prioritization, and allocation to ensure programs and projects within the Disease Area are optimally supported.Ensures timely and high-quality delivery of departmental deliverables.Participates in and/or leads cross-functional and cross-sector initiatives.QualificationsA university/college degree in a scientific discipline is required plus at least 14 years of relevant pharmaceutical/scientific experience. At least 12 years of relevant medical writing experience is required. At least 5 years of people management experience is required.Qualities and CharacteristicsAbility to lead in a team environment.Expert project management skills.Demonstrated ability to collaborate internally and develop effective partnerships with key business partners.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
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