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Global nuclear medicine pharmaceutical company is seeking an experienced corporate and transactionalLegal Counsel/Assistant General Counsel (title depending on experience) to be part of the US in-house legal team based in the Northern New Jersey office. There is an opportunity to work in the NYC office as well.
This position reports directly to the Global General Counsel.
The company has a strong pipeline of products and has mainted double-digit annual growth in sales for the past 9 years. It is headquartered abroad and has US headquarters in Manhattan. The company focuses its development on molecular imaging and individualized therapy (personalized medicine) for patients with serious conditions.
Participating in all aspects of legal operations to support continued corporate growth, including pharmaceutical industry compliance, corporate and securities matters and contract negotiation;
Advising the commercial business on pharmaceutical regulatory matters and compliance laws, regulations, industry standards and company policies that arise throughout the product lifecycle;
Providing legal advice and business counsel on innovative marketing and sales strategies, activities and programs, including review of advertising and promotional strategies and materials, and working with clients to develop appropriate and compliance policies and strategies for interacting with healthcare providers and other stakeholders;
Responsible for policy development, implementation and training;
Overseeing and managing a wide variety of agreements including services agreements, clinical trial agreements, co-commercialization agreements, confidentiality agreements, license agreements, supply and distribution agreements, consulting agreements, and other commercial and R&D agreements, in support of the commercial business;
Maintaining corporate records for a variety of subsidiaries and other aspects of the corporate secretary function;
Assisting with M&A, securiites filings, subsidiary management, employment law matters, insurance procurement, litigation oversight and other duties/responsibilities as assigned;
Coordinating and managing legal matters handled by outside counsel;
Assisting in the preparation of Board of Directors and shareholder meetings;
Partnering with executive, research, operations, finance and human resources colleagues on various matters.
JD and at least 6+ years practicing law at a major law firm and/or life sciences company with significant relevant pharmaceutical regulatory experience;
Deep understanding of pharmaceutical regulatory environment;
Experience designing and implementing programs and policies pertaining to pharmaceutical regulations;
Demonstrated expertise with negotiating and drafting complex agreements;
Corporate, M&A and/or public company experience preferred;
Ability to analyze and advise the business on consideration and implementation of appropriate and practice legal strategy;
Sound legal and business judgment with the ability to problem-solve in a high-output, fast-moving environment;
Customer-focused and ability to interact with all levels of the organization;
Exceptional interpersonal, written and oral communication skills;
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