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Medical Writer

Location: UK
Company: Johnson & Johnson
Johnson & Johnson
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Janssen Research & Development, L.L.C., a member of Johnson & Johnson's Family of Companies, is recruiting for a Medical Writer /Sr Medical Writer in the Titusville, New Jersey area, U.K., Europe, Belgium, Switzerland, or Canada. Remote work options may be considered, on a case-by-case basis and if approved by the Company! Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, hematology, immunology, neuroscience, infectious diseases, cardiovascular, metabolic, mental health, and pain management, and vaccines, and cardiovascular and metabolic diseases. Please visit http://www.JanssenRnD.com for more information. Janssen thrives on a diverse company culture, celebrating the uniqueness of our employees and is committed to inclusion. Janssen is proud to be an equal opportunity employer. Our culture is interconnected by the shared values of Our Credo. It is a culture that celebrates diversity and diverse perspectives, and helps its employees achieve an effective balance between work and home life and supports their efforts to have a positive impact on their communities. Position Summary: Learns the medical writing role within the pharmaceutical industry and business. Works in a team environment and matrix. Able to write and coordinate basic documents independently and more complex documents (within the therapeutic area [TA]) under supervision. May prepare documents across TAs under close supervision. May function as a lead writer on a project, indication, or a compound either early- or late-stage in life cycle under close supervision. May actively participate in process working groups.Principal Responsibilities: Writes or coordinates clinical and regulatory documents such as, but not limited to, CSRs, IBs, protocols, summary documents and regulatory responses of lower complexity, and RMPs. 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. Works in a team environment with increasing independence for longer-term activities and takes an active role on assigned projects with respect to timing, scheduling, and tracking. Able to guide or train cross-functional team members on processes and best practices. May lead early- or late-stage compound writing teams with close supervision. Regularly meets with manager and mentors and attends departmental meetings. Attends cross-functional meetings as appropriate (eg, project kick-off and review meetings, study team meetings, Global Program Team meetings). Maintains and applies knowledge of industry, company, and regulatory guidelines. Completes all time reporting, training, metrics database, and project tracking updates as required in relevant company systems. May mentor more junior staff on document planning, processes, content, or provide peer review. #GIFTS Qualifications Education and Experience Requirements: A university/college degree is required. An advanced degree (eg, Masters, PhD, MD) is preferred. At least 4 years of relevant pharmaceutical/scientific experience is required. At least 2 years of relevant clinical/regulatory writing experience is required.Other: Strong oral and written communication skills. Recognizes how to best interpret, summarize, and present statistical and medical information to ensure quality and accuracy of content, under supervision. 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 basic problems independently and more complex problems under close supervision. Demonstrates learning agility. Builds solid and productive relationships with cross-functional team members. Learns and applies knowledge of regulatory guidance documents such as ICH requirements. At Johnson & Johnson, were on a mission to change the trajectory of health for humanity. That starts by creating the worlds healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work. Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com. Primary Location United States-New Jersey-Titusville-1125 Trenton Harbourton Road Other Locations North America-Canada, Europe/Middle East/Africa-Switzerland, Europe/Middle East/Africa-United Kingdom, Europe/Middle East/Africa Organization Janssen Research & Development, LLC (6084) Job Function R&D
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