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2 Days Ago
3 Locations
Junior
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Associate Project Manager will ensure client satisfaction in managing ICON's Central Laboratories services. The role includes project coordination, adherence to protocols, communication with stakeholders, and monitoring study budgets. Other responsibilities include preparing management reports, representing ICON in meetings, and mentoring junior team members.
3 Days Ago
2 Locations
Expert/Leader
Expert/Leader
Healthtech • Biotech • Pharmaceutical • Manufacturing
The VP of Biometrics will lead ICON's Strategic Services Biometrics team, overseeing projects in pharmacovigilance, medical writing, and regulatory affairs, while ensuring client satisfaction, managing budgets, coordinating across departments, and driving business development.
Top Skills: Sas,R
3 Days Ago
Dublin, IRL
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Director of Group Accounting & Reporting will ensure compliance with public reporting obligations under US GAAP and IFRS, advise on annual reports, oversee financial reporting, and manage complex accounting issues. The role involves liaising with various teams and leading pre-deal reviews for potential acquisitions.
3 Days Ago
Dublin, IRL
Mid level
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Quality Control Analyst II is responsible for sustaining the global quality control program across ICON Laboratories. Key responsibilities include data management, analysis, regulatory compliance, and facilitating performance improvements through statistical insights. The role requires engagement in audits and preparation of quality summaries for senior management, while contributing to process improvements and collaboration with laboratory personnel.
3 Days Ago
7 Locations
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Principal Biostatistician, you will lead statistical activities in clinical trials, interpret medical data, and oversee study protocol sections. You are responsible for statistical consulting, proposal preparation, and client interactions to support clinical development efforts.
Top Skills: BiostatisticsStatistics
3 Days Ago
8 Locations
Senior level
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
As a Senior Statistical Programmer, you will lead projects, manage multi-disciplinary teams, and program statistical analyses/reports, specifically focusing on CDISC ADaM programming and data analysis. Responsibilities include developing and validating data structures, writing departmental macros, and training team members.
Top Skills: AdamCdisc
3 Days Ago
2 Locations
Junior
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Site Services Specialist I will provide technical support regarding protocol requirements, address queries from investigator sites, sponsors, and CRAs, perform minor database updates, and manage supplies and kits for sites. This role requires effective communication and the ability to work under tight deadlines.
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