Senior Director, Regulatory Clinical Strategy

Pacira Pharmaceuticals, Inc.•Parsippany-Troy Hills, NJ

About The Position

This role directs, manages, evaluates and implements regulatory projects in support of company goals in the area of clinical strategy. The position will play a major role in shaping cohesive regulatory strategy across the assigned programs and ensuring effective integration of broad regulatory ideas/tactics supporting program/platform strategy. This role’s responsibilities may be global, regional, or local based on programs status.

Requirements

Bachelor's degree in a life science with a minimum of 10 years progressively responsible experience in Regulatory Affairs in the U.S. pharmaceutical industry; or
Master’s degree in a life science with a minimum of 8 years progressively responsible experience in Regulatory Affairs in the U.S. pharmaceutical industry; or
Doctoral (M.D., Ph.D., Pharm.D., etc.) degree with a minimum 6 years progressively responsible experience in Regulatory Affairs in the U.S. pharmaceutical industry
Demonstrated expertise in creating and assessing proposals to regulatory authorities on regulatory paths and clinical plans, and in leading productive health authority interactions, including well organized preparation of cross functional teams
A business-minded leader, capable of strategic thinking and proposing innovative solutions to regulatory problems
Must have demonstrated advanced proficiency in analyzing and interpreting data, protocols, safety reporting, labeling, and other activities related to the phases of drug development for assigned products
Demonstrated expertise in analyzing the adequacy of proposed regulatory pathways and strategies and guiding development teams with recommendations for change/refinements based on ongoing regulatory outcomes throughout development
Able to articulate the organization’s strategic vision and core values, and successfully contribute to improving the quality of internal regulatory policies, programs, and initiatives
Demonstrates excellent communication skills with ability to impact and influence the decisions of a team, communicates with all levels within the company and act as liaison/representative both internally and externally, and communicates effectively in writing and in verbal presentations regulatory strategy plans and submission documents
Demonstrated ability to provide regulatory leadership on a cross-functional team and work effectively in a matrix environment
Demonstrated technical expertise in regulatory affairs science including advanced knowledge of regulatory frameworks and external environments
Expert knowledge of global/regional/local regulatory legislation, laws, procedure, and guidance for pharmaceutical development of medicines for human use, with demonstrated knowledge of the research and development, nonclinical and clinical requirements related to drug development, registration, and maintenance of human pharma. Excellent written and oral English communication skills
Experience working within, and potentially managing, the Medical, Legal and Regulatory review process of promotional materials
Experience and knowledge in the preparation of and post-approval management of prescription drug, biological, and/or medical device labeling
Experience working with FDA's OPDP and submission of promotional materials
Advanced knowledge of regulations and guidances related to the commercialization of pharmaceutical, biological, and/or medical device products in the US; experience in other global regions is preferred
Outstanding written and verbal communication skills
Excellent analytical and critical thinking skills
Demonstrated negotiation and problem-solving skills
Strong project management skills with keen attention to detail
Expert knowledge of MS Word and ability to ensure adherence to internal templates and standards for regulatory submission documents
Results-oriented with an enthusiastic attitude and strong interpersonal skills
Proven attention to detail, while at the same time seeing the big strategic picture

Nice To Haves

Managerial experience desirable

Responsibilities

Lead the development of regulatory strategy for multiple and/or complex projects (from first-in-human to post-marketing application stage) outlined in Global Regulatory Strategy Documents, including for regulatory submissions documents and HA communications.
Analyze and address complex issues, providing advanced regulatory solutions and guidance to cross-functional teams and regulatory leadership. Advise senior management on status of global regulatory affairs strategies and tactics, practice, and procedures.
Align with cross-functional teams to lead the development and management of project plans and timelines, followed by effective execution of the plan by ensuring all projects are appropriately prioritized and key goals are met on time.
Influence regulatory environment by active participation in relevant conferences, trade associations, industry/agency regulatory meetings, committees; remain up-to-date on changing regulatory environment, and provide regulatory policy and intelligence including competitive issues that influence regulatory strategy.
Supervise and mentor direct reports to facilitate professional growth; identify training opportunities and provide mentoring to ensure individuals are appropriately developed in accordance with their roles and responsibilities.
Identify resourcing needs and appropriate allocation activities to internal and external support.
Drive continuous process improvements to enable an efficient and lean organization.
Support budgeting and forecasting for function and Regulatory Affairs department.
Manage vendors and contractors as applicable.
Other responsibilities as needed.