Drives the successful and timely execution of a clinical research protocol from study start-up to final clinical study report within established budget and timelines using strong project management and organizational skills, monitors protocol progress and addresses and manages obstacles, serves as primary operational contact for the protocol, coordinates the development of protocol level documents and plans, effectively leads a global team of individuals assigned to the protocol; strong interpersonal and influencing skills, proven team-building skills and ability to foster partnerships across projects and multidisciplinary teams, effective oral and written communication skills to influence, inform or guide others.
A minimum of a BA or BS Degree with 4 to 6 years of demonstrated project management experience of which at least 2 should have been gained in the pharmaceutical or healthcare industry. This candidate should have leadership experience in the execution of global clinical research trials management.
Additional PTM support is needed to manage the current BoW for the I-O priority programs. The demand for this program continues to increase with multiple upcoming submissions and an expanding LCM program.