**Group Purpose**

To prepare scientific and regulatory submission documents that comply with global regulatory standards.

**Job Summary**

To author and gain approval of scientific and regulatory submission documents that comply with global regulatory standards. To maintain key business relationships with appropriate cross-functional product team members. This role serves as functional area lead on product teams, leads writing activities for complex product submissions providing functional area expertise, trains and mentors more junior writers, and leads departmental activities.

**Key Activities**

Independently:

+ Author or oversee the authoring of all regulatory submission documents 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, Pedi...