The remote Senior Medical Writer is responsible for providing clinical regulatory document support to the clinical teams, ensuring successful preparation of high-quality submission-ready documents and effective implementation of the clinical writing process. Provides medical writing expertise for multiple compounds/devices and/or projects within various therapeutic areas (Oncology and aesthetics strongly preferred, immunology preferred). Interfaces with external groups (e.g., PK, Toxicology, eSubmissions, Regulatory, Statistical Support, Data Management, Clinical, Publishing) to ensure accurate and timely completion/delivery of information and review of clinical regulatory submissions.
•Serves as medical writing lead on clinical regulatory documents. Works closely with the Regulatory team(s) on document strategies. Implements all activities related to the preparation and compilation of data and information into a single comprehensive package for new and updated clinical regulatory documents (US and ex-US).
•Coordinates the review, approval, and other appropriate functions involved in the production of clinical regulatory projects. Arranges and conducts review meetings with the team. Ensures required documentation is obtained.
•Converts relevant data and information into a form that meets clinical regulatory document requirements. Explains data in manner consistent with the target audience(s) or clinical regulatory requirements.
•Effectively communicates clinical regulatory document deliverables needed, writing process, and timelines to team members. Holds team members accountable to agreed-upon project dates and with an appropriate quality level. Negotiates with functional areas on project outcomes and deliverables to meet conflicting demands. Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or elevation as appropriate.
•Understands, assimilates, and interprets sources of information with appropriate guidance/direction from development teams. Interprets and explains data generated from a variety of sources. Verifies that results are consistent with protocols. Challenges conclusions when necessary. Understands/complies with appropriate conventions, proper grammar usage, and correct format requirements per ICH and other governing bodies.
•Understands/complies with appropriate conventions, proper grammar usage, and correct format requirements per ICH and other governing bodies following applicable divisional guidelines, templates, and SOPs.
•Performs literature searches as needed for drafting document content. Interprets literature information and makes recommendations for application to clinical regulatory documents.
•Works with Regulatory Quality Assurance throughout clinical regulatory document audit process, answers questions during the audit process (as appropriate), and works with team to draft responses as necessary.
•Knowledgeable of US and international regulations, requirements, and guidance associated with clinical regulatory document preparation and submissions. Must continually train/be compliant with all current industry requirements as they relate to clinical regulatory submissions, including electronic submission/approval standards.
•Serves as a department representative on project teams. Acts as Subject Matter Expert for assigned clinical teams regarding computer-based technologies utilized by the respective departments (e.g. COSMOS, ARCH, eCTD). May mentor and provide guidance to more junior medical writers and/or external vendor/agencies. Implements tactical process improvements.
•Bachelor of Science required, with relevant writing experience, or Bachelor's degree in English or communications, with relevant science experience.
•American Medical Writing Association (AMWA) certification or other is preferred, with a specialty in Editing/Writing or Pharmaceutical.
•3 years relevant industry experience in medical writing in the healthcare industry or academia required or in a related area such as quality, regulatory, clinical research, or product support/R&D. Clinical regulatory device writing experience preferred.
•3 years experience in experimental design and clinical/preclinical data interpretation preferred.
•Knowledgeable of US and international regulations, requirements and guidance associated with clinical regulatory document preparation and submissions. Knowledge of Medical Device Regulation (MDR) preferred.
•Knowledge and experience with Common Technical Document content templates. Working knowledge of current electronic document management systems and information technology.
•Excellent written and oral communication skills. Experience in working with collaborative, cross-functional teams, including project management experience.
•Ability to assimilate and interpret scientific content and translate information for appropriate audience.
•Superior attention to detail. Ability to find and correct errors in spelling, punctuation, grammar, consistency, clarity and accuracy.
•Expert in word processing, flow diagrams, and spreadsheets. Excellent working knowledge of software programs in Windows environment.
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity and affirmative action employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. If you would like to view a copy of the company’s affirmative action plan or policy statement, please email CorpJat_ABV@abbvie.com.