Location: Remote, OR
quality reviewers, and cross-functional teams (e. g. SMT, CDT, process improvement committees), in order to create/author/manage documentation required to support clinical trials and regulatory submissions. Successful candidate will participate in cross-functional teams and influences decision making.
They may lead strategy discussions related to document development and make recommendations for process improvements within department and participates in discussions to implement change. Principal Accountabilities· Independently prepares moderately complex clinical documents for one or more programs; coordinates preparation of clinical documents by other writers with minimal supervision·
Represents department on clinical teams (e. g. SMT, CDT); leads document-related meetings; reviews statistical analysis plans and clinical data reports as needed· Mentors junior writers on departmental processes related to document preparation (e.
g. planning document-related meetings, developing document timelines); reviews documents written by junior writers for content and format· Participates on departmental initiatives Qualifications· Master’s required in a life science or health discipline. Ph D preferred· 1+ yrs. regulatory writing experience within a life science organization· Ability to interpret data within a specific therapeutic area (neuroscience ideal)· Solid understanding
of standard clinical document types· Solid understanding of internal and external guidelines related to document preparation· Strong written and oral communication skills· Strong organizational and meeting skills Additional Information Why Biogen?
Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve.
We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to interaction, gender identity or expression, interactionual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law.
Biogen is an E-Verify Employer in the United States. This employer is a corporate member of my Gwork - LGBTQ+ professionals, the business community for LGBTQ+ professionals, students, inclusive employers & anyone who believes in workplace equality. For more details: jobs-search. org/sciences_oregon-r782079/senior-medical-writer-remote_i1966598820
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