Senior Medical Writer – Early Development Services

This is a fully remote position, open to applicants in Netherlands.

📋 Description

• Act as the lead author for routine documents such as clinical study reports and study protocols.

• Compile and summarize data from clinical trials.

• Support the creation of more intricate clinical and scientific documents.

• Ensure adherence to quality processes and standards.

• Provide assistance in program management tasks, including timelines, budgets, and forecasts.

• Represent the department during project launch and review meetings.

⛳️ Requirements

• A Bachelor's degree in a scientific field or an equivalent formal academic/vocational qualification is required; an advanced degree is preferred.

• Experience in regulatory writing that equips the candidate with the necessary knowledge, skills, and abilities for the role (equivalent to 5+ years).

• Required experience in the pharmaceutical or CRO industry.

• Proven track record in managing and directing complex medical writing projects is necessary.

• Experience in early-phase projects is preferred.

🏝️ Benefits

• Award-winning learning and development program.

• Competitive salary.

• Comprehensive benefits package focused on the health and well-being of employees.

• Flexible working culture.

• Emphasis on work-life balance.