
Associate Director, Regulatory Medical Writing Job at Scorpion Therapeutics in N
Scorpion Therapeutics, New Bremen, OH, United States
Role Summary
Associate Director, Regulatory Medical Writing will represent Medical Writing and provide leadership across compound areas, oversee junior writers, and assist in leading regulatory submissions. We work closely with senior Medical Writing management to help produce and ensure adherence to department guidelines, templates, standard timelines, and SOPs that follow regulatory guidelines. Responsibility will also include managing and developing staff; this may include performance management and training. Additionally, you will independently write all in-scope clinical documentation in their compound areas. This position can be either fully remote or on-site at our Sleepy Hollow, NY or Warren, NJ offices.
Responsibilities
Leads all MW deliverable work for assigned compounds/indications
Manages work of both internal and outsourced Medical Writers
Works with clinical team to develop document strategy and write in-scope deliverables as needed
Develop and articulates document strategy and timelines
Identifies appropriate decision makers, focuses on results/actions
Leads regulatory submissions/submission document writing
Participates in process improvement initiatives, working groups, etc. within MW and throughout Global Development
Participates in new initiatives within MW and throughout Global Development
Manages processes and organize priorities; solves problems; fosters collaboration to resolve conflict
Leads, challenges, and develops MW team
Manages and develops staff; this may include performance management, recruiting, coaching, and training
Ensures adherence to applicable guidelines, templates and SOPs for all MW documents provided for therapeutic area
Remains compliant with internal training
Qualifications
Minimum of 8 years’ relevant Medical Writing experience (relevant advanced degree may offset some of the experience requirement)
Expert knowledge of the clinical research process and regulations/guidelines and regulatory writing
Expert clinical document reading, writing, and editing experience
Any experience managing medical writers is helpfulProficiency in MS Word, Adobe Acrobat, PowerPoint, and electronic document management systems
Thorough understanding of ICH GCP guidelines
Education
Bachelor’s degree required; advanced degree preferred
#J-18808-Ljbffr