Flexible Work, Better Balance
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Sr. Regulatory Affairs Specialist to join our diverse and dynamic team. As a Sr. Regulatory Affairs Specialist at ICON, you will complete country and/or regional Clinical Trial Regulatory deliverables according to study specifics, ICON policies, procedures, applicable regulations and the principles of ICH‑GCP with sound scientific/technical principles in line with contractual agreement.
Depending upon experience, you may become involved, when required, in staff training/mentoring and contribute to the review of ICON systems and procedures as appropriate.