Lead Clinical Data Manager

Overview

As a Senior Clinical Data Science Lead/Lead Clinical Data Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

Primary Location: Poland (remote)

What you will be doing:

• Lead end to end data review activities performed on a clinical trial as a Lead Data Manager.
• Accountable for achieving clinical data science deliverables on-time, with high- quality and to agreed financial metrics.
• Serve as primary point of contact for internal and external team members regarding clinical data review activities and leads these data review activities to ensure delivery of data fit for analysis.
• Provides input into clinical system development activities and clinical risk management activities.
• Oversees the collection of all clinical trial data from multiple sources.
• Performs DM vendor oversight activities across multiple studies. Reviews and gives input in vendor oversight processes.
• Review Key Risk Indicators (KRIs) outputs in aggregate across sites, regions and countries. As needed, review study level operational and patient data to support the investigation and root cause analysis of observations.
• Provides training and subject matter expertise to lower-level DM peers. 
• Collaborate with clinical operations, investigators, and other stakeholders to ensure smooth data flow throughout the trial.

Qualifications

You should have:

• 8+ years related experience in pharmaceutical, clinical research or health services industry with a minimum of 6 years’ experience as Data Manager with progressive levels of responsibility. 
• Degree qualified in a relevant Scientific or Healthcare discipline.
• Good knowledge of clinical data science activities (Data review, risk management & analytics, clinical systems).
• Very strong subject matter expertise in the Data Management (DM) discipline. Ability to support multiple studies concurrently with little to no oversight by functional manager.
• Strong computer skills, including database management software, reporting tools, medical coding tools, and solid understanding of Central Monitoring tools etc. 
• Strong understanding of different types of data sources in a clinical trial setting and/or expertise with external data types. 
• Engaging, supportive and you lead by example.

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

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsAt ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodationsInterested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.