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Global parental leave for all new parents (maternal, paternal, adoptive or surrogacy-assisted).
Global exercise reimbursement.
Two weeks off (one of them fully paid) for volunteer work.
Principal Medical Writing Scientist Integrated Data Analytics and Reporting (IDAR) Janssen Pharmaceutical Companies of Johnson & Johnson is recruiting for a Principal Medical Writing Scientist, based in the UK Who is Janssen? We’re more than 30,000 people working hard to prevent, treat, cure and stop some of the most devastating and complex diseases of our time. From heart disease to HIV, Alzheimer’s disease to cancer, we are committed to issues that touch everyone’s lives. Our mission is to transform individual lives and fundamentally change the way diseases are handled, interpreted, and prevented. We believe that challenging something is the best way to change it. So, every day, in more than 150 countries, we bring cutting-edge science and the most creative minds in the industry together to think differently about diseases. We aim not only to innovate but also to empower people with the tools they need to make informed decisions and achieve the best possible results for their health. We are looking at a future where the world of healthcare will be challenged by informed and empowered patients. We work for change that will improve access to medicines: the best available treatment at an affordable price. That’s why we at Janssen strive to provide access to effective and affordable medicines and related healthcare services to the people who need them. Position Summary: Able to write and coordinate basic and complex documents, independently when working within own TA, and under supervision when working across TAs. Leads in a team environment and matrix. Able to function as a lead MW on most compounds, under supervision. May actively participate in or lead process working groups. Provides input into functional tactics/strategy (eg, writing teams, process working groups). Highly proficient in the use of internal systems, tools, and processes. Principal Responsibilities: Writes or coordinates clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents, RMPs, regulatory responses, and briefing documents. Leads cross-functional (eg, with clinical team) document planning and review meetings. Interacts with cross-functional colleagues on document content and champions MW processes and best practices. Responsible for establishing document timelines and strategies in accordance with internal processes, with some mentorship from functional management and clinical team, as needed. Completes all time reporting, training, metrics database, and project tracking updates as required in relevant company systems. Able to function as a lead writer on most compounds (or submissions, indications, or disease areas) under supervision. Is primary point of contact for medical writing activities for the cross-functional team (eg, clinical). Coaches or mentors more junior staff on document planning, processes, and content. Provides peer review as needed. May actively participate in or lead process working groups. Principal Relationships: May interact with or oversee day-to-day work by contractors or external service providers as needed under supervision. May collaborate with external partner company staff on codeveloped compounds. Qualifications Education and Experience Requirements: A university/college degree is required. An advanced degree (eg Masters, PhD, MD) is preferred. At least 6 years of relevant pharmaceutical/scientific experience is required. At least 4 years of relevant clinical/regulatory medical writing experience is required. Other: Recognizes 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. Excellent oral and written communication skills. Attention to detail. Ability to function in a team environment. Organizes time well. Strong leadership skills, both in project and process management as well as in time management (influencing, negotiating, assertiveness, taking initiative). Resolves complex problems under supervision. Demonstrates learning agility. Builds solid and productive relationships with cross-functional team members. #Gifts Primary Location United Kingdom-England-High Wycombe- Organization Janssen Cilag Ltd. (7360) Job Function R&D Requisition ID 2206027800W
Child care benefits
Short term disability