Clinical Study Manager

Clinical Careers Page(1 month ago)

HybridFull TimeSenior$132,075 - $177,906 (estimated)Clinical Operations

About this role

A Clinical Study Manager at ICON is assigned to a pharmaceutical sponsor within the RATIO (R&D Asset Transition and Integration Office) team to lead or support Post Trial Access (PTA) activities. The role operates within clinical development to ensure assigned clinical programs progress through transition and integration activities. The position interfaces with internal clinical operations leadership and external partners to represent the study at program level.

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Required Skills

Project Management
Clinical Operations
ICH GCP
Regulatory Compliance
Budget Management
Vendor Oversight
Risk Management
Timeline Management
Data Management
TMF Management

+5 more

Qualifications

Bachelor's Degree
Life Sciences Preferred

About Clinical Careers Page

iconplc.com

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.

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