Novato, CA, United States
Manager, Pharmaceutical, Editing, Writing
Jan 06, 2021
Apr 21, 2021
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Why Join Us?
Be a hero for our rare disease patients
Ultragenyx is a commercial-stage biopharmaceutical company committed to developing novel therapies for the treatment of rare and ultra-rare genetic diseases. The company has rapidly built a diverse portfolio of small molecule, monoclonal antibody, mRNA and gene therapy candidates with the potential to address debilitating genetic diseases for which the unmet medical need is high, the biology for treatment is clear, and for which there are typically no approved therapies treating the underlying disease.
Developing new treatments for rare genetic diseases is challenging work. It takes courage, talent, and dedication to look past the easy answers and uncover new solutions that can make a meaningful impact. At Ultragenyx we push each other to perform at our very best, because we never lose sight of our mission – to make a difference in our patients’ lives.
Come join our team during this exciting time of growth and opportunities! During the COVID-19 Outbreak we are committed to our hiring process. The health and safety of our employees and prospective employees take priority which means at this time our process will include WebEx video discussions, interviews & onboarding.
dedicated – Your biggest challenges yield rare possibilities
The Senior Manager, Medical Writing will be responsible for writing and coordinating the writing of peer-reviewed scientific publications, including distribution of work to contract medical writers or agencies as needed. This is an individual contributor position with team leadership responsibilities. The Senior Manager, Medical Writing will work closely with investigators and cross-functional teams to ensure the publications are high quality and completed in a timely fashion compliant with SOPs, Good Publication Practice guidelines, and company goals. The core duties of the Senior Manager, Medical Writing are delineated below.
Responsibilities including, but not limited to:
Interact with external authors and key internal stakeholders to develop high-quality publications (manuscripts, abstracts, posters, slide presentations) for peer-reviewed journals and scientific congresses.
Liaise closely with the Publication Planner to ensure alignment with timelines and data communication plans
Ensure smooth and effective document management from initial outline to published version
Distill large amounts of clinical and scientific data into essential elements for graphical display
Partner with the lead author to oversee document review, comment adjudication, and version control
Perform literature-based research to support writing activities
Develop best practices for authoring and reviewing
May attend and provide support at Scientific Congresses
BS, MS, or doctorate in a scientific or medical field
2 to 5 years publications experience in the biotechnology/pharmaceutical industry preferred
In-house experience strongly preferred
Demonstrated experience analyzing and communicating scientific data in peer-reviewed scientific publications; knowledge of publication guidelines (i.e., ICMJE, GPP3) and best practices
Demonstrated experience in medical writing, editing, and clinical development
Strong leadership, planning, and project management skills, along with initiative and ability to be productive with minimal supervision and minimal administrative support
Demonstrated ability to work effectively in a fast-paced environment with multiple high priority projects
Proven ability to implement medical writing processes and standards
Exceptional oral and written communication skills
Understands and effectively responds to multicultural communication styles and business practices with alliance partners and internal colleagues
Flexible; adapts work style to meet organization needs
Strong organizational abilities and experience in a multitasking environment
Motivated, self-directed, and able to work autonomously and in team settings to meet aggressive organizational goals
Dedication to quality and reliability
Excellent computer skills (Microsoft Office Suite, Adobe Illustrator, GraphPad Prism); graphics expertise a plus
Ability to build and maintain effective partnerships, both internally and externally
Holds self and others accountable for adherence to high ethical standards; adopts and maintains the utmost integrity and respect for colleagues at all levels
Rare disease experience and a strong understanding of bone disease or metabolic genetics preferred
Ultragenyx Pharmaceutical is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital and veteran status. Reasonable accommodation will be provided for qualified individuals with disabilities and for qualified disabled veterans in job application procedures, as required by applicable law. If you have any difficulty using our online application system and need an accommodation due to a disability, you may contact Talent Acquisition by calling: (415) 483-8800 or by emailing us at
. For electronic email and mail inquiries, please include a description of your requested accommodation, your name and contact information.
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: All candidate activity and open positions are managed strictly through our Human Resources Department. Our Human Resources Department kindly requests that recruiters not contact employees/hiring managers directly in an attempt to solicit business and present candidates. Please note that failure to comply with this request will be a factor in determining a professional relationship with our organization. Submission of unsolicited resumes prior to an agreement set in place between the Human Resources Department and the recruiting agency will not create any implied obligation. Inquiries on developing a recruiting relationship with us, may be directed to :
Website : http://www.ultragenyx.com