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Medical Writer
4 days ago
Purpose:
Medical Affairs (MA) brings deep medical expertise to healthcare providers and payers. MA focuses on answering their questions with customized clinical and real-world evidence that can make the difference on if and how they use products. Additionally, MA brings clinical insights from customers back to the company to inform new product development and lifecycle planning. MA also supports patients with educational tools to help them manage their illness and with assistance to access our medicines for those facing tough financial situations. The MA content development team will be key in maintaining and creating content to support Medical Affairs activities such as:
Slide Updates
Internal Training Slides
Manuscript Slides
Data Slides
Newsletters/ bulletin
QR Compendium
Affiliate Regional Slides
HCP & patient education material
Advisory board slides
Competitive landscape slides
Image sourcing, image redraws
Lexicon
MQAD (Medical Questions Analysis Document)
Minimum Qualification Requirements:
Bachelor’s degree in a scientific, health, communications, technology health related field.
Demonstrated experience in technical/ regulatory scientific writing.
Strong communication and interpersonal skills.
Successful completion of writing exercise (a writing exercise is required as part of the candidate evaluation process)
Other Information/Additional Preferences:
Graduate degree with formal research component or in life sciences.
Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.
Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise).
Experience writing regulatory, clinical trial documents and/or publications
Experience writing deliverables for Medical Affairs communications (slide decks, patient or HCP materials, etc)
Experience in clinical development, clinical trial process or regulatory activities.
Demonstrated project management and time management skills.
Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates).
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