Principal Medical Writing Scientist, Oncology Late Development (1 Of 2) (Aplica Ya)

.DescriptionAt the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing, and preventing some of the most devastating and complex diseases of our time.Janssen Research & Development discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, pulmonary hypertension, and cardiovascular and metabolic diseases.Within Integrated Data Analytics & Reporting (IDAR), the Regulatory Medical Writing team are recruiting for a Principal Medical Writing Scientist to support our Oncology - Late Development (1 of 2) therapeutic area. This position is open globally and may be located in Europe (eg, United Kingdom, Ireland, Belgium, Netherlands, Germany, France, Spain, Italy, Poland, Bulgaria or Switzerland), North America (eg, Spring House, PA, Raritan, NJ, Titusville, NJ, or Canada), or other countries. Remote work options may be considered on a case-by-case basis and if approved by the company.Are you ready to join our team? Then please read further!Key Responsibilities:Prepare and finalize clinical documents such as, but not limited to, clinical study reports, investigator's brochures, study protocols, summary documents, risk management plans, regulatory responses, and briefing documents.Lead cross-functional document planning and review meetings. Interact with peer writers and colleagues from other departments. Able to lead program-level or submission writing teams with supervision. Able to lead process working groups.Coach or mentor more junior writers on document planning, processes, content, and provide peer review as needed.· Responsible for establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed.· If a lead writer for a program: Be the primary point of contact and champion for medical writing activities for the clinical team. Responsible for planning, setting strategy, and leading writing group for assigned program.· Maintain and apply knowledge of the industry, company, and regulatory guidelines.QualificationsUniversity/college degree required. Masters or PhD preferred.At least 6 years of relevant pharmaceutical/scientific experience.At least 4 years of relevant medical writing experience.Oncology experience is preferred.Ability to recognize how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content in complex document types under general supervision is required.Strong attention to detail is required.Strong oral and written communication skills is required.Strong leadership skills, both in time management as well as in project/process management. Able to resolve complex problems under supervision is requiredDemonstrate learning agility is required