Regulatory Medical Writing Manager
1 month ago
Lifelancer, a talent-hiring platform in Life Sciences, Pharma and IT, is seeking an experienced Regulatory Medical Writing Manager to support our Oncology therapeutic area. This role may be located in the UK, other European countries, or Canada.
We value a colleague with at least 8 years of relevant pharmaceutical/scientific experience and at least 6 years of relevant medical writing experience. If a people manager, preferably up to 2 years of people management experience is required.
The successful candidate will have excellent oral and written communication skills, expert project/time management skills, strong project/process leadership skills, and the ability to recognize how to best interpret, summarize, and present statistical and medical information.
This position offers a competitive estimated salary of $120,000 - $180,000 per annum, depending on location and experience.
Job DescriptionThis is a critical role in our Integrated Data Analytics Reporting (IDAR) team, where you will lead a team environment, work with a high level of independence, and take a lead role on assigned projects with respect to content and scientific strategy, timing, scheduling, and tracking.
- Prepare and finalize all types of clinical documents.
- Lead project-level/submission/indication writing teams.
- Maintain knowledge of industry, company, and regulatory guidelines.
- Coach or mentor more junior staff on document planning, processes, content, and provide peer review as needed.
We are looking for someone with:
- Oncology therapeutic area experience preferred.
- University/college degree required; Masters or PhD preferred.
- Able to build and maintain solid and positive relationships with cross-functional team members.
- Demonstrate learning agility.
This role offers the opportunity to work with a talented team, contribute to the development of innovative medical solutions, and grow your career in a dynamic industry.
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