Global Regulatory Writing Manager

Roles & Responsibilities :

• Author regulatory submission documents, as assigned, including Clinical Study Reports, Investigator Brochures, Responses to Questions, Protocols, Protocol Amendments, Informed Consent Forms, Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, Pediatric Investigation Plans, and other regulatory documents;
• Conduct the formal review and approval of authored documents, following applicable standard operating procedures;
• With considerable supervision, manage regulatory writing activities for product submissions, including new and supplemental drug applications / biologics license applications;
• Serve as functional area lead on product teams (e.g., Global Regulatory Team, Evidence Generation Team, Global Safety Team, Label Working Group)
• May provide functional area input for Global Regulatory Plan and team goals
• May work with contract and freelance writers
• May participate in training and mentoring of junior medical writers
• May participate in departmental and cross-departmental initiatives, as appropriate.
• Generate document timelines, with team input
• Keep abreast of relevant professional information and technology

What we expect of you

Basic Qualifications :

Preferred Qualifications :

Functional Skills :

Soft Skills :

Skills Required

Gcp, Project Management, Ms Office