Senior Medical Writing Lead - AI-Enabled Clinical Dossiers

Almirall, S.A; España; On-site; PHP 5,528,255 - 7,985,257; Full time

Benefits offered by this job

Top Employer recognition

Professional development opportunities

Job summary

Almirall, S.A is searching for a Medical Writing Senior Manager to lead the development of high-quality clinical and regulatory documents that support R&D programs.

This role involves cross-functional collaboration, ensuring regulatory compliance, and leveraging AI technologies to enhance writing processes. Candidates should have 8+ years in medical writing and an advanced degree.

Join a company recognized as a Top Employer and contribute to transforming patients' lives.

Qualifications

• Minimum 8 years of experience in medical writing within the pharmaceutical or biotech industry.
• Proven track record in authoring and managing clinical and regulatory documents for global submissions.
• Fluent in English.

Responsibilities

• Lead the planning, writing, and review of various clinical and regulatory documents.
• Work closely with cross-functional teams to gather scientific input.
• Review and edit documents for scientific accuracy and adherence to standards.
• Manage external medical writing vendors and ensure quality standards.

Skills

Clinical document writing

Regulatory compliance

Cross-functional collaboration

AI/GenAI tools

Strong communication skills

Education

Advanced degree in Life Sciences (PhD, PharmD, MD, MSc)

Tools

Document management systems

Job description

Almirall, S.A is searching for a Medical Writing Senior Manager to lead the development of high-quality clinical and regulatory documents that support R&D programs.

This role involves cross-functional collaboration, ensuring regulatory compliance, and leveraging AI technologies to enhance writing processes. Candidates should have 8+ years in medical writing and an advanced degree.

Join a company recognized as a Top Employer and contribute to transforming patients' lives.