Study Start-up Specialist (Sponsor dedicated)

Clinical Careers Page

11 days ago

Remote

Full Time

Medior

0 applicants

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About this role

ICON plc is seeking a Study Start Up Associate II to oversee the initiation of clinical trials by managing regulatory submissions and coordinating with stakeholders to ensure compliance and approval processes are efficient. The role involves supporting study teams and improving start-up procedures.

Skills

Qualifications

Bachelor's degree in life sciences or related fieldMinimum of 2 years in clinical research or regulatory affairs

About Clinical Careers Page

iconplc.com

Industry

Healthcare

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.