Annexon Biosciences

Senior Director, Medical Writing

San Francisco Bay Area · Director

Sponsorship not specified$257k-$286kDetected 5 days ago

Data VisualizationClinical TrialsFDA RegulatoryPharmacovigilanceScientific WritingResearchCommunicationCollaborationProblem SolvingWritingMicrosoft OfficeSharePoint

About the role

For more information on Annexon and our pipeline, check out our site Annexon Biosciences & Annexon Pipeline.
We trade on Nasdaq under the ticker symbol ANNX and are headquartered in Brisbane, CA.
We're seeking exceptional talent from all backgrounds to fuel our growth.

Responsibilities

In partnership with cross-functional teams, critically analyze and interpret non-clinical and clinical data (internal and external) to develop crucial strategy, conclusions, and messaging.
As needed, perform literature and scientific database searches in support of analyses and development of background summaries.
Participate on teams as a key thought leader to develop strategy and approach, ensuring consistency and efficiency with how messaging and documents are built and organized, contributing scientific knowledge and analytical skills.
As needed, collaborate with internal and external authors/vendors in support of the development of written deliverables, overseeing operational considerations and ensuring awareness of expectations, milestones, and deliverables.
We believe that our differences enable us to be a better team - one that makes better decisions, drives innovation, and delivers better business results.
You will collaborate closely with teams to develop realistic timelines to meet writing deliverables and program goals.

Nice to have

Capability and comfort with prioritizing multiple projects, deliverables, and timelines to exercise thoughtful judgment, problem-solving and decision-making.
Ability to think ahead and identify opportunities for change and improvement with an emphasis on operations and efficiency.
Superior attention to detail and thoroughness related to processes, consistency, grammar, syntax, and scientific accuracy.
A leader and role model who operates with an entrepreneurial spirit, integrity, independence, transparency, and exemplifies the Annexon core values with a focus on improving the lives of patients and families.

Skills

Prior work history at a biotech or pharmaceutical company preferred, smaller company environment ideal.

Compensation

$257,000 - $286,000 USD

Benefits

Build a scalable medical and scientific writing infrastructure, with an emphasis on resourcing, that includes developing formats, templates, processes and standards, style guides, workflow, and operating procedures.
A stimulating and rewarding workplace includes flexible work schedules, remote opportunities and the ability to achieve a work-life balance.

Company info

At Annexon Biosciences we are a biopharmaceutical company advancing a late-stage clinical platform of novel therapies for people living with devastating classical complement-mediated neuroinflammatory diseases of the body, brain, and eye.
With proof-of concept data in Guillain-Barré syndrome, Huntington's disease and geographic atrophy, we are rigorously advancing our mid-to late-stage clinical trials to bring new potential treatments to patients as quickly as possible.
At Annexon, you'll be part of a team committed to making an impact together.
At Annexon, we're building a diverse, equitable, and inclusive workplace.
We value unique perspectives and unconventional paths.
If you're the best candidate for the job, even if you don't perfectly fit the traditional mold, we encourage you to apply.
Learn more about our commitment to diversity, equity, inclusion, and our company culture!
Our novel scientific approach targets upstream C1q to block the classical complement inflammatory cascade before it starts, and its therapeutic candidates are designed to provide meaningful benefits across multiple autoimmune, neurodegenerative and ophthalmic diseases.
The Senior Director, Medical and Scientific Writing plays a critical role within the organization.
Reporting to the SVP, Regulatory, Quality and Pharmacovigilance, you will work in partnership with a talented and collaborative team across our Clinical, Regulatory, Quality, Medical Affairs, Commercial and CMC departments to author and drive development of key documents in support of all of our programs.
You will be empowered to interpret data, formulate messaging, and strategize on the development of Clinical and Regulatory documents.

Equal opportunity

Equal Opportunity Employer, and we prohibit discrimination or harassment of any kind.

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