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Benefits offered by this job
Generous paid time off
Educational assistance programs
401(k) plan
Job summary
A leading biotechnology company is seeking a Medical Writing Science Senior Manager to author complex clinical regulatory documents. The role demands exceptional writing and project management skills, alongside a Ph.D. and significant experience in clinical writing. This hybrid position allows for remote work. Key responsibilities include leading writing efforts, ensuring compliance, and collaborating with cross-functional teams. A competitive pay range, annual bonuses, and extensive benefits are offered, making it an excellent opportunity for qualified candidates.
Qualifications
6 years of experience or equivalent combination of education and experience.
Ability to manage challenging, high-value projects.
Initiative in solving complex problems.
Responsibilities
Author complex clinical regulatory documents.
Lead Medical Writing for pivotal clinical studies.
Ensure compliance with company and industry standards.
Skills
Outstanding written and oral communication skills
Experience writing and editing clinical regulatory documents
Ability to analyze, interpret, and summarize complex data
Project management and organizational skills
Education
Bachelor's degree in relevant discipline
Ph.D. (or equivalent degree)
Job description
A leading biotechnology company is seeking a Medical Writing Science Senior Manager to author complex clinical regulatory documents. The role demands exceptional writing and project management skills, alongside a Ph.D. and significant experience in clinical writing. This hybrid position allows for remote work. Key responsibilities include leading writing efforts, ensuring compliance, and collaborating with cross-functional teams. A competitive pay range, annual bonuses, and extensive benefits are offered, making it an excellent opportunity for qualified candidates.