Earl Lambert, Msj

Earl Lambert, Msj

Neurology Sales Specialist @ Supernus Pharmaceuticals

About Earl Lambert, Msj

Earl Lambert is a Neurology Sales Specialist at Supernus Pharmaceuticals, Inc., with extensive experience in the pharmaceutical industry. He holds a Master of Science in Jurisprudence from Seton Hall University and has a strong background in health law and compliance.

Work at Supernus Pharmaceuticals

Earl Lambert has been serving as a Neurology Sales Specialist at Supernus Pharmaceuticals, Inc. since 2021. In this role, he operates in New Jersey, focusing on the neurology sector within the pharmaceutical industry. His responsibilities include engaging healthcare professionals, promoting products, and providing information to support patient care. Lambert's position reflects his commitment to advancing neurological health solutions.

Previous Experience in Pharmaceutical Sales

Prior to his current role, Earl Lambert worked at QuintilesIMS as a Specialty Sales Representative from 2013 to 2020. His tenure lasted seven years, during which he operated in the South Jersey and Greater Philadelphia areas. Before that, he was a Professional Sales Representative at Janssen, Pharmaceutical Companies of Johnson and Johnson for three years. Lambert also held the position of Psychiatry Specialty Manager and Area Field Sales Trainer at Wyeth Pharmaceutical / Pfizer from 2002 to 2010, covering the Tri-State Area.

Education and Expertise

Earl Lambert earned a Master of Science in Jurisprudence (MSJ) with Magna Cum Laude honors from Seton Hall University School of Law, specializing in Pharmaceutical and Medical Device Law & Compliance from 2013 to 2015. He also holds a Bachelor of Science (B.S.) degree in Business Administration and Management from Lebanon Valley College. His educational background supports his expertise in health law and compliance.

Knowledge of Health Law and Compliance

Earl Lambert possesses extensive knowledge of health law and compliance, including regulations such as the Prescription Drug Marketing Act (PDMA) under 21 CFR 203, drug labeling requirements under 202.1, the Sunshine Act, and the PhRMA Code. His understanding of these regulations aids in identifying, evaluating, and mitigating risks within the healthcare industry, ensuring adherence to federal and state laws.

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