argenx
Senior Medical Writer
United States - Remote · Senior
Sponsorship not specified$104k-$143kDetected 27 days ago
Computer VisionPharmacovigilanceCommunicationTime ManagementMicrosoft Office
About the role
- This individual will execute the overall strategy for all medical writing processes according to argenx medical writing standards and corporate objectives.
- This range reflects our good faith estimate at the time of posting.
- This means actual pay may differ from the posted range when justified by these factors.
Responsibilities
- Supports the lead writer and project teams to ensure project deadlines are met
- Basic understanding of scientific methodology as applied to drug development, including the phases, processes, and techniques used within a clinical development environment from protocol design through regulatory submission
Nice to have
- Bachelor's degree in a scientific or clinical discipline or related field is required
Skills
- Bachelor's degree in a scientific or clinical discipline or related field is required; Ph.D. preferred
- Native/bilingual or fluent American English proficiency
- Solution-focused
- Experience with Veeva Vault and Please Review
- Experience with implementing lean writing techniques
- Familiarity with pharmacovigilance guidelines and developing aggregate reports
- Ability to work precisely according to procedures and regulations
- Ability to prioritize and multi-task successfully in a fast-paced environment
- Ability to work autonomously, as well as in a team
- Excellent written and verbal communication skills
- Excellent time management skills and a proven ability to work on multiple projects at any given time
- Must be proficient in MS Office
Compensation
- For applicants in the United States: The annual base salary hiring range for this position is $104,000.00 - $143,000.00 USD.
- The annual base salary hiring range for this position is $104,000.00 - $143,000.00 USD.
Benefits
- Individual compensation is determined using objective, inclusive, and job-related criteria such as relevant experience, skills, demonstrated competencies and internal equity.
- It also includes a comprehensive benefits package, including but not limited to retirement savings plans, health benefits and other benefits subject to the terms of the applicable plans and program guidelines.
- Responsible for inspection-readiness of medical writing activities
- Minimum of 3 years of related, sponsor-level pharma or biotech clinical/regulatory medical writing experience required; CRO experience considered
Equal opportunity
- If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@argenx.com.
- Only inquiries related to an accommodation request will receive a response.
Visa & Work Authorization
- Minimum of 3 years of related, sponsor-level pharma or biotech clinical/regulatory medical writing experience required; CRO experience considered
This listing is sourced directly from argenx's careers page and normalized into a canonical job model.