Remote Director, Regulatory Medical Writing — Global Leader

Teva Pharmaceutical Industries Ltd.; Remote; USD 177,000 - 234,000; Full time

Job summary

A global pharmaceutical company is seeking a Director in Global Regulatory Medical Writing. This role involves writing and editing clinical regulatory documents, overseeing resources and vendors, and ensuring compliance with regulations. Ideal candidates should have a PhD/PharmD with extensive experience and strong writing skills. A competitive benefits package is offered, including health insurance and retirement savings.

Benefits

Comprehensive Health Insurance

401(k) with employer match

Paid Time Off

Life and Disability Protection

Qualifications

• Expertise in preparing complex regulatory documents.
• Experience in overseeing training and resource management.
• Ability to ensure regulatory compliance in submissions.

Responsibilities

• Write and edit clinical regulatory documents.
• Oversee contingent workers and vendors.
• Lead the preparation of document templates.

Skills

Regulatory medical writing expertise

Strong writing/editing skills

Knowledge of drug development regulations

Mastery of Microsoft Word

Education

PhD/PharmD with minimum 8 years experience

Master’s with minimum of 10 years experience

Job description

A global pharmaceutical company is seeking a Director in Global Regulatory Medical Writing. This role involves writing and editing clinical regulatory documents, overseeing resources and vendors, and ensuring compliance with regulations. Ideal candidates should have a PhD/PharmD with extensive experience and strong writing skills. A competitive benefits package is offered, including health insurance and retirement savings.