Kiaema Reid is Associate Director of Regulatory in the firm’s New York office, focusing on life sciences regulatory and compliance issues relating to marketing and commercial interactions with healthcare professionals. Kiaema regularly manages and supports pharmaceutical, medical device and biotechnology companies to ensure compliance with federal and state fraud and abuse laws, FDA regulations, state and federal laws and industry guidelines relating to interactions with healthcare professionals.
Kiaema has held a senior manager position at a life sciences company and she has significant experience with developing, operationalizing and managing policies and procedures relating to commercial interactions with health care professionals. She also has experience with training commercial and vendor personnel to ensure conformance with standard operating procedures.
Kiaema is certified in healthcare compliance. She has co-authored multiple publications, including “Sunny Side Up: A New Era of State and Federal Aggregate Spend and Marketing Disclosure Laws,” published in the Pharmaceutical and Medical Device Compliance Manual.
- Seton Hall University Law School, M.S.J.
- Seton Hall University, Healthcare Compliance Certificate Program
- Fairleigh Dickinson University, Paralegal Certificate
- Fairleigh Dickinson University, B.A.