Remote Senior Medical Writing Lead, Global

Biopharma Asia; Alabama; Remote; USD 166,000 - 248,000; Full time

Job summary

Boehringer Ingelheim is seeking an Associate Director of Medical Writing to devise and execute document strategy and timelines in clinical development programs. You will independently write and manage key global clinical documents, mentor internal and external writers, and contribute to cross-functional SOP development.

Remote position with global scope; strong expertise in regulatory medical writing, clinical documents, and project leadership is required.

Qualifications

• Advanced degree in life sciences with regulatory writing experience preferred.
• Strong knowledge of regulatory writing standards and regulatory guidelines.
• Excellent written and verbal English communication skills.

Responsibilities

• Assume project medical writer role across early clinical development; coordinate with functions, plan timelines, write key clinical documents and oversee external writers.
• Develop document strategies for project and study-level documents; manage review comments and timelines.

Skills

Regulatory writing

Medical writing

English fluency

Education

Advanced degree in life sciences

Master's degree with relevant experience

Bachelor's degree with experience

Job description

Boehringer Ingelheim is seeking an Associate Director of Medical Writing to devise and execute document strategy and timelines in clinical development programs. You will independently write and manage key global clinical documents, mentor internal and external writers, and contribute to cross-functional SOP development.

Remote position with global scope; strong expertise in regulatory medical writing, clinical documents, and project leadership is required.