● 10+ years of Biotech/Pharma clinical research related experience, at a Director or Senior Director level of scope and seniority.
● Strong vendor management and oversight experience.
● Strong experience in oncology.
● Proven ability working on a global team in the management and completion of multiple, complex clinical studies.
● Competent in application of standard business procedures (SOPs, ICH, global regulations, ethics and compliance).
● Integral participation in initiatives or advancement strategies for clinical operations.
● Experience in successful study initiation through study completion, and in multiple phases of studies (Phases 1-3).
● Strong communication and stakeholder management skills.
● Boston-based, with willingness to be onsite in our Seaport office a minimum of 2 days per week.
● Legally authorized to work in the United States.