Individuals selected for these positions will schedule and supervise clinical projects with
PRA, provide leadership in the delivery of services to clients; review work produced by project
teams; ensure staff fulfills their responsibilities in accordance with project contracts and
PRA policies, procedures and SOP’s. They will also be responsible for taking a lead role in the
day-today management of major studies; ensure that projects are delivered on time, within
budget and according to client expectations.

Depending on level of positions, successful candidates must at minimum, possess an
undergraduate degree in a clinical or health related field: advanced degree preferred, along
with a minimum 3-5 years experience as a Clinical Project Manager with a CRO or Pharmaceutical
company. This position also requires a minimum of 3 years of experience in project scheduling,
managing resources and budgets and coordinating team activities, as well as experience with the
full clinical development process through regulatory submissions.  Project Director positions
must have a minimum of 7 years experience, past supervisory experience, as well experience
running large global trials. Both positions require candidates to be detailed-oriented,
computer proficient in a Windows environment and possess superior interpersonal and
organizational skills.