Keren Nadler Niv
About Keren Nadler Niv
Keren Nadler Niv is the Site Contracts Lead at Bristol Myers Squibb in Israel, with extensive experience in legal counsel and advocacy roles in the pharmaceutical and medical sectors.
Current Role at Bristol Myers Squibb
Keren Nadler Niv currently serves as the Site Contracts Lead at Bristol Myers Squibb in Israel. In this role, she is responsible for the creation and negotiation of clinical trial agreements with pharmaceutical and medical device companies worldwide. Her responsibilities include drafting, reviewing, and finalizing contracts to ensure compliance with regulatory standards and company policies.
Previous Experience as Legal Counsel at Hadassah
Keren Nadler Niv worked as a Legal Counsel at Hadassah from 2016 to 2020 in the Jerusalem Area, Israel. In this position, she provided legal counseling to senior management and the clinical trials department. She was responsible for creating and negotiating consortium agreements, reviewing insurance terms for clinical trials, and developing internal policies and Standard Operating Procedures (SOPs). Additionally, she advised on regulation, Ministry of Health guidelines, insurance matters, and commercial agreements.
Advocate Career
Keren Nadler Niv's extensive experience as an Advocate spans multiple firms. She worked at Gross Orad Schlimoff & Co. for ten years (2010-2020), Bentzur & Co. Law for five years (2005-2010), and Haim Zadok & Co., Advocates for one year (2004-2005). At these firms, she honed her skills in legal counseling, commercial agreements, and institutional policy development.
Educational Background
Keren Nadler Niv studied at IDC Hertzlia from 1999 to 2003, earning dual degrees in Law (LL.B.) and Business Administration and Management. Her educational background provided a strong foundation in legal principles and business management, which supports her professional roles in legal counseling and contract negotiations.
Expertise in GMP & GDP Regulations
Keren Nadler Niv has unique expertise in GMP (Good Manufacturing Practice) and GDP (Good Distribution Practice) regulations and guidelines. This specialized knowledge plays a critical role in her responsibilities at Bristol Myers Squibb, where she ensures that clinical trial agreements and other contracts meet rigorous regulatory standards. Her expertise in these regulations helps maintain quality and compliance throughout the clinical trial process.