Cont Coord

The primary purpose and objective of the Contract Coordinator position is to work with and assist the Contract Analysts in the completion and execution of contracts with clinical study sites and principal investigators ("Clinical Trial Agreements").

**The primary duties of the Contract Coordinator include**: (i) preparation and monitoring of Clinical Trial Agreements from initial site contact through execution of agreements (the "CTA Process"); (ii) maintain and handle open lines of communication between PPD clinical teams and investigator sites during the CTA Process; and (iii) provide technical and administrative support to Contract Analysts during the CTA Process.

**Education and Experience**: High School Diploma2 years administrative experienceOr equivalent combination of education and experience that provides the knowledge, skills, and abilities to perform the job Knowledge, Skills and Abilities: Excellent organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectivelyFlexibility to reprioritize workload to meet changing project timelinesResponsible for understanding and adhering to PPD and Client SOPs, WPDs and other regulations for all aspects of project implementation, execution and closeoutExcellent English and grammar skillsProficient in MS Word and ExcelMust be able to work independently 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.