Principal Clinical Data Science Lead

OVERVIEW OF THE ROLE:

The Principal Clinical Data Science Lead role is part of the Early Phase Data Management department and is responsible for managing data management teams, studies, and programs of studies under the general direction of the Senior Manager/Director of Data Management. The Principal Clinical Data Science Lead will provide planning estimates for project scope, schedule, and resource requirements, and ensures that studies are properly managed and delivered. They will work with Clinical Operations, Biostatistics, SAS Programming, Medical Writing, and Quality Assurance to ensure that data collected during trials is managed according to corporate standards and meets regulatory guidelines for data integrity.

The Early Phase service line of the company specializes in the strategic development, management, and analysis of studies and programs that support Phase 1/2a clinical development.

The Principal Clinical Data Science Lead will manage a number of fast moving early phase studies or programs of studies to ensure project objectives are met within budget, to agreed timelines, and to a high level of quality. As a DMPM, you will manage a global team of clinical data management resources. The Principal Clinical Data Science Lead will provide input into CRF design, protocol review, edit check specifications, data entry conventions, monitoring guidelines, and any other study related documents and will be responsible for the maintenance, cleaning, and lock of the EDC study databases.

Additional Responsibilities:

• Review the project contract in order to ensure that any out-of-scope work is managed promptly and efficiently
• Manage the overall project budget throughout the life cycle of the project, taking overall responsibility for cost control, timelines, and project quality
• Negotiate with clients and/or external customers/departments in relations to timelines and key deliverables
• Travel (approximately 15%) domestic and/or international.

TO BE SUCCESSFUL, YOU WILL NEED:

• 6+ years of clinical data management experience (in a Clinical Research Organization or Pharmaceutical company)
• 3+ years of experience leading studies with key responsibilities for study set-up and close-out tasks
• Experience with Phase I studies strongly preferred, but not require
• Experience with Rave strongly preferred, but must have experience with at least one of ICON’s preferred CDMS (e.g. Rave, Inform, Oracle Clinical, OCRDC, UX EDC)
• Highly computer literate, including strong Microsoft Office skills
• Excellent communication and interpersonal skills
• Strong client relationship management skills
• Excellent organizational and planning skills as well as a demonstrated aptitude for project management
• Bachelors degree or local equivalent in a scientific field and/or equivalent experience
• EMEA based location

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

ICON, including subsidiaries, is an equal opportunity and inclusive employer and 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 or submit a request here.

Interested 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.