Associate Director, Study Start-Up
Core
Lead the strategic development and management of the Study Start-Up team in Europe, overseeing regulatory submissions and client relationships for clinical trials.
Role type
Senior IC clinical operations manager (Study Start-Up)
Builds
Clinical trial protocols and regulatory submissions for biotech/pharma clients
Domain
Clinical research / CRO / Life sciences
Required skills
Study Start-Up leadership, regulatory submission management, client relationship management, team management, process improvement, business development input
Preferred skills
Advanced degree in life sciences, experience in oncology/cardiology/metabolic/CNS/anti-viral/anti-infective areas
Technologies
Clinical trial management systems, regulatory submission platforms
Responsibilities
Contribute to the growth and strategic development of the Study Start-Up team; Develop and identify continuous improvement opportunities of internal processes; Oversee Study Start-Up/Regulatory Submission activities and timelines; Provide input on new business development opportunities; Develop and maintain relationships with clients; Support the local German team development.
