Central Monitor

As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

**Key Responsibilities**:
- Lead and oversee clinical trial risk management activities, including identification, assessment, and mitigation of study-related risks throughout the clinical trial lifecycle.- Utilize strong clinical and monitoring experience (central and site) to ensure high-quality data collection, analysis, and reporting.- Conduct clinical data analytics to identify risk signals, trends, and outliers to proactively manage and mitigate trial risks.- Collaborate cross-functionally across global and country teams to ensure alignment with clinical development strategies and compliance with international regulations and company standards.-
- Leverage advanced digital tools, e-databases, and risk-based monitoring platforms to enhance trial oversight and reporting.- Manage timelines and deliverables effectively, demonstrating strong project management skills.- Foster an inclusive and collaborative team environment by recognizing diverse talents, working styles, and cultural contexts.- Support transformation initiatives by integrating AI and advanced analytics into clinical trial processes.**You are**:
- Minimum of 5 years of recent experience in the pharmaceutical industry, including clinical research within pharmaceutical companies or CROs.- At least 3 years of comprehensive experience in clinical monitoring (central and/or site), clinical data analytics, data management, or related fields.
- Experience Working in Cluepoint- Deep understanding of the clinical trial management process, including protocol interpretation, study risk assessment, and risk management methodologies.- In-depth knowledge of global drug development processes, regulatory environments, and industry best practices.- Demonstrated critical thinking and analytical skills with the ability to interpret complex clinical data and drive actionable insights.- Strong communication, coordination, and stakeholder management skills.- Proven ability to work effectively within a global, matrixed organizational structure.- Proficiency in using digital clinical tools and analytics platforms.- Experience in project management with a track record of delivering projects on time.- Awareness of team dynamics and experience fostering collaborative, high-performing teams.- Experience in clinical trial transformation efforts, including AI and analytics integration.- Ability to navigate diverse cultural environments and promote inclusion.

**What ICON can offer you**:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others