Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI and San Diego, CA. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need.
The Position
The Associate Director, Regulatory/Medical Writing collaborates with members of cross‑functional teams to prepare high-quality regulatory and clinical documentation for submission to global regulatory agencies including the preparation of components for INDs/NDAs, annual reports, Orphan Drug Designation applications, and briefing books as well as clinical study documentation such as protocols, investigator brochures, etc as required within agreed-upon timelines. The Associate Director also assists with the preparation of publications, abstracts, and other external communications in support of Arrowhead business functions. The Associate Director also assists in implementing processes and standards to ensure company scientific documents are prepared to the highest editorial standards and quality.
Responsibilities
- Prepares, edits, and finalizes protocols, investigator brochures, synopses, clinical study reports, regulatory documents (INDs/NDAs, annual reports, Orphan Drug Designation applications, Agency Response to Questions, briefing books, etc)
- Prepares related clinical documents, such as abstracts, posters, presentations, and manuscripts
- Collaborates with and manages contract medical writers as required for project assignments
- Advises and assists in the review and management of nonclinical and CMC technical reports as required
- Develops and maintains company house-standard templates and best review practices for regulatory and clinical documentation. Ensure vendors and contractors maintain company standards
- Participates in regulatory and clinical team strategy meetings to ensure that that results and messages in clinical documents accurately reflect the data in tables, figures, and listings (TFLs) and other information sources Partners with the scientific staff including participation in the review of mock and/or blinded TFLs, and narrative planning for relevant documents
- Assists in the development and maintenance of Development Core Product Data Sheets, draft labeling, and company work instructions and SOPs, as requested
- Ensures that medical writing deliverables conform to International Conference on Harmonization (ICH) and other relevant regulatory guidelines and medical editorial boards
- Manages the document review process ensuring conflicting and/or ambiguous comments are clarified and appropriately addressed. Schedules and conducts document-related meetings including kickoff meetings and document review planning and alignment discussions to ensure documentation timelines are achieved
- Ensures documents are generated in accordance with agreed internal processes and standards, are submission ready, and are appropriately stored in appropriate document management system(s)
- Ensures that appropriate documented quality control (QC) checks are performed on regulatory/medical writing deliverables, responds to findings, and recommends quality process improvements
Requirements:
- Bachelor's degree in medically related field or life science
- 6 to 8 years of relevant medical writing experience in the pharmaceutical industry is essential
- Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research and medical writing standards; demonstrated ability to interpret and apply these guidelines to document writing. Familiarity with basic statistical analysis concepts and techniques is required
- A demonstrated track record of contribution to successful regulatory components used in filings eg, IND/CTAs, NDA/BLA/MAAs is important
- Prior experience in interacting with cross-functional study team members is essential
- Highly proficient in the use of MS Word, Excel, Endnote, Adobe Acrobat, PowerPoint, and structured document templates
Preferred:
- Post-graduate degree (master's or doctoral)
- Experience with electronic document management systems
- Experience writing in one or more of the company's key therapeutic areas eg, liver disease, respiratory disease, or rare diseases
- Membership in professional medical writing, regulatory, or drug information associations
California pay range
$160,000—$185,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
All applicants must have authorization to work in the US for a company.
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