Draft, review and negotiate agreements with clinical study sites and principal investigators ("Clinical Trial Agreements").
Serve as the primary contact for all Clinical Trial Agreements for all clinical studies assigned to his / her group and must be able to work independently, while consulting with Company attorneys and other key individuals as appropriate and necessary.
Draft and review CTA and associated contracts related to CTAs according to Company policy, rules, practices and procedures and implement and manage the process for internal and external approval, execution and filing of CTAs and associated contracts.
Identify and assist with the implementation of process improvement opportunities. Maintain contact and relationships with all internal departments, Senior Management and clients and shall identify and protect PPD and its clients from unnecessary business and legal risks.
Education and Experience :
Knowledge, Skills and Abilities :
Pharmaceutical Product Development, LLC is firmly committed to Equal Employment Opportunity (EEO) and prohibits employment discrimination for employees and applicants based on age, race, color, pregnancy, gender, gender identity, sexual orientation, national origin, religion, marital status, citizenship, disability or protected veteran or other status protected by federal, state, and / or local law.