Associate Director, Remote Global Medical Writing Lead

BioCT; Ridgefield (CT); Remote; USD 166,000 - 248,000; Full time

Benefits offered by this job

Discretionary bonus

Relocation assistance

Job summary

Boehringer Ingelheim is seeking an Associate Director of Medical Writing to devise and execute document strategy for global clinical programs, leading cross-functional teams and mentoring internal and external writers.

You will oversee key regulatory documents, ensure quality/timeliness, and advance SOPs while collaborating with function leaders. This remote-based leadership role requires deep regulatory writing expertise and strong English communication.

Qualifications

• Advanced degree (PharmD/PhD/MD) with at least 4 years in regulatory medical writing.
• Experience as project medical writer and regulatory writing expertise.
• Strong knowledge of global regulatory guidelines and standards.
• Excellent written and verbal English skills; strong communication.

Responsibilities

• Lead medical writing across early clinical development and plan timelines.
• Oversee clinical documents and mentor internal/external writers.
• Ensure quality and timeliness of documents with external providers.
• Participate in cross-functional groups and SOP development.
• Apply regulatory guidelines and maintain SOP compliance.

Skills

Regulatory writing

Clinical development

Project management

Mentoring/training

Cross-functional collaboration

Excellent English writing

Education

Advanced degree (PharmD/PhD/MD)

Master's degree +6 years or Bachelor's +8 years experience

Experience as project medical writer

Tools

Microsoft Word

Microsoft PowerPoint

Job description

Boehringer Ingelheim is seeking an Associate Director of Medical Writing to devise and execute document strategy for global clinical programs, leading cross-functional teams and mentoring internal and external writers.

You will oversee key regulatory documents, ensure quality/timeliness, and advance SOPs while collaborating with function leaders. This remote-based leadership role requires deep regulatory writing expertise and strong English communication.