Jobs in Murcia, Spain

Job summary

A leading biopharmaceutical solutions organization is seeking a Senior Regulatory Medical Writer to lead the completion of pivotal medical writing deliverables. This remote role requires excellent communication skills and a strong understanding of regulatory standards. Responsibilities include generating clinical study reports, protocols, and other essential documents for regulatory submissions. Join our team to contribute to life-changing therapies globally while working in a culture that values diversity and innovation.

Benefits

Qualifications

• Proven experience in medical writing, particularly for regulatory documents.
• Strong understanding of regulatory standards and guidelines.
• Excellent communication skills.

Responsibilities

• Lead the completion of medical writing deliverables while ensuring clarity and accuracy.
• Manage medical writing activities across studies.
• Complete various regulatory documents like clinical study protocols and reports.