Consultant - FDA amp Life Sciences

Profile

King & Spalding, a leading global law firm, seeks a FDA & Life Sciences Consultant to join our Washington, D.C. office.u00A0 Under general supervision and according to established policies, the Consultant will perform a variety of duties assisting attorneys and clients of the Food and Drug/Life Sciences Team.u00A0u00A0u00A0The firm offers a generous total compensation package with bonuses and raises awarded in recognition of individual merit-based performance. Eligible employees may participate in King & Spaldingu2019s comprehensive benefit program including health and wellness plan, life and disability insurance, flexible spending accounts and a health savings account, a 401(k) plan, profit sharing plan, on-site gym access, discount programs, an onsite childcare center and a substantial Paid Time Off (PTO) program.u00A0u00A0u00A0Candidates will have the following responsibilities:u00A0u00A0Identify high-impact regulatory and analytical problems, monitor developments of interest to our clients and team members, synthesize insights across research and trends, provide thoughtful responses;u00A0u00A0Establish strong trusted relationships with client teams and regulators;u00A0Aid in developing and providing insights into research approaches and applications for products, including next generation products;u00A0Assist clients and team members in a variety of regulatory submissions, including product applications for both tobacco products, ENDS products, and other next generation products;u00A0Understand and evaluate products relating to risk continuum;u00A0Conduct research regarding FDA action; analyze and provide insight into FDA actions;u00A0Work with clients and team members to synthesize research data and analysis into strategic implicationsu00A0u00A0Provide written comments and feedback to regulator actions, including proposed regulation and enforcement actions;u00A0Communicate effectively with external parties, including regulators and key stakeholdersu00A0Support both the regulatory and litigation teams assisting with work on FDA matters that relate to science and/or policy including getting products to market, enforcement actions, etc.;u00A0Assist with case/trial preparation for Food & Drug related investigations and litigation; including, but not limited to, file and database management.u00A0u00A0Qualifications/Experience:u00A0Candidate must have recent Center for Tobacco Products (CTP) experience and must have relevant industry experience.u00A0Bacheloru2019s degree required; graduate degree in life science or chemistry is strongly preferred.u00A0We are proud of our remarkably cohesive culture, which now encompasses 2,300 lawyers and business professionals in 23 offices worldwide. We seek to attract and develop the very best talent to work with us.u00A0u00A0King & Spalding LLP (K&S) is committed to providing equal employment opportunity to all applicants and employees in full compliance with all state, federal, and local laws prohibiting discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, age, disability or any other status protected by applicable law.u00A0

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