Executive Principal, ICO (Strategic Regulatory & Safety)
About the role
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ICON was acknowledged by Forbes as a 2018 Top Large Sized Employer in America
Would you like the opportunity to join ICON as a leader of our Regulatory & Quality Services team? Apply here to learn more about this leadership role and ICON’s “Own It” Culture!
About the Executive Principal, ICO (Regulatory Services) at ICON:
Location: Any U.S. ICON Office or Home-Based
At ICON you will provide leadership for Regulatory and Quality Services groups (Pharmaceutical, OTC, and Device, combination products Biologics, Biosimilars and Generics), Scientific Affairs, and Regulatory Operations Teams. Develop organizational strategy and growth plans globally. You will be responsible for overall leadership of personnel including training and development. You will be accountable for financial targets, project execution and delivery for regulatory requirements. You will develop strategies to build and grow the business and to effectively deliver regulatory and regulatory operations services globally.
You will collaborate closely across development of clinical trials, marketing application, life-cycles and marketed products. Interact with clients and leadership to ensure consistent performance and quality of work as you develop strong customer relationships at the senior management level and ensure project teams are managing Client expectations. Facilitate client meetings with the regulatory agencies and in collaboration with Expert Advisory Committee Meetings Provide Support to Business Development, including strategic consulting in relation to client opportunities (internal and external).
Benefits of working at ICON:
ICON offers an exceptional executive benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, management bonus plan, restricted stock units, and enough time away from work to keep balanced. We provide you and the teams with the tools, innovation and resources to be successful in ensuring utmost compliance, operational efficiencies, and continued growth tracks.
To succeed you will need:
BS degree in Life Sciences; MS or PhD preferred or equivalent job experience and minimum of 15 years of regulatory experience in the Pharmaceutical or Biotech Industry. Knowledge of applicable Regulatory guidelines and regulations. We are looking for strong interpersonal skills and ability to build and maintain relationships internally and externally. Experience with management of global budgets and P&L. Ability to influence/work across functional units to achieve desired results. Experience in consulting an asset and expertise in managing and developing global teams.
What’s Next?
Following your application if you are successful you will be invited to an initial telephone interview with one of our dedicated recruiters who will be able to provide you with more details of this opportunity.
We invite you to review our opportunities at www.iconplc.com/careers.
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment
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Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
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