Associate Director, Ra Global Regulatory Strategy - Boston, United States - AbbVie

AbbVie

Verified Company

Boston, United States

1 week ago

Posted by:

Mark Lane

beBee recruiter

Description

Company Description

The Associate Director, RA Global Regulatory Strategy, US & Canada (Oncology) is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development.

This individual demonstrates the ability to combine knowledge of scientific, regulatory & business issues to enable development and commercialization of products that are developed, manufactured, or distributed to meet relevant US and Canada regulatory requirements.

This individual assures that regulatory strategies defined within the GRPT are effectively implemented and maintained in line with changing regulatory and business needs.

Responsibilities:

This individual has responsibility for products/multiple driver indications for a product within a Therapeutic Area and supports the Global Regulatory Lead (GRL, Director), in the development & execution of the regulatory strategy. Area of responsibility has significant regulatory impact and possibly significant impact to ABBV overall.
Manages interface with Health Authority (FDA) for key projects/issues, including direct collaboration with review division personnel.
May also serves as primary liaison and interfaces with FDA for meetings, teleconferences and coordinates preparation of FDA meeting briefing packages and responses.
Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial.
Demonstrates excellent negotiation skills, problem solving skills and builds consensus.
Operates independently, with recognition of when to consult management.
Makes decisions and plans for operations (workflow, assignments, staff development) within area of responsibility with mínimal direction.
Assists in the development, training, and mentoring of staff members.
Demonstrates solid understanding of current US and Canada regulations and guidance, political and legal climate, and industry practices to assist in meeting organizational goals.
Presents pertinent regulatory information to appropriate crossfunctional areas.
Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP).

Significant Work Activities -Keyboard use (greater or equal to 50% of the workday)

Qualifications

Required Education: Bachelor's Degree (pharmacy, biology, pharmacology) or related life sciences.
Preferred Education: Relevant advanced degree is preferred. Certification a plus.

Required Experience: 8 years Regulatory, R&D or Industry-related experience.
Preferred Experience: 5 years in pharmaceutical regulatory affairs.

Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization.
Extensive experience interfacing with government Agencies and Health Authority personnel.
Able to deliver challenging messages effectively without compromising important business relationships.
Experience working in a complex and matrix environment.
Demonstrated success in negotiation skills, strategic thinking, and credibility within the organization.
Strong communication skills, both oral and written.
Proven skill at implementing successful US and Canada regulatory strategies; global regulatory experience is a plus.

**Additional Information