Clinical Data Science Lead

Reposted 2 Days Ago
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Mexico City, Cuauhtémoc, Mexico City
In-Office
Mid level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
The Clinical Data Science Lead manages clinical data review activities, ensures timely data delivery, forecasts budgets, and collaborates with cross-functional teams to maintain data quality and compliance.
Summary Generated by Built In
Clinical Data Science Lead - Mexico - Office with Flex

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We have an incredible opportunity for a Clinical Data Science Lead to join ICON's Full-Service IOD Clinical Data Science team. The Clinical Data Science Lead (CDSL) serves as the primary contact for internal and external team members regarding clinical data science data review activities and leads these review activities to ensure the delivery of data fit for analysis.  

What You Will Be Doing:

  • Develop and oversee the timeliness of clinical data science activities during the life cycle of studies as it relates to data review and data delivery milestones 

  • Works independently and with other project leads, as needed, to negotiate timelines and key deliverables with clients and/or external customers, vendors and departments 

  • Participates in Sponsor and/or third-party audits 

  • Forecasts budget, hours and resourcing for clinical data review activities 

  • Performs analytic review as defined in the scope of work and functional plans focusing on errors that matter or have a meaningful impact on the safety of the subject or interpretation of the final analysis 

  • Work and collaborate with cross-functional and global groups 

  • Provide input into clinical system development activities and clinical risk management activities 

  • Accountable for the development of planning documents related to data review, data analytics and data deliverables 

  • Establishes approach and leads resources to achieve operational and strategic plans

  • Tracks and keeps functional management and those responsible for project management informed of any issues that might affect project target dates, scope, or budget, and escalates potential problems effectively and in a timely manner 

  • For problem solving, use existing procedures to solve problems where solutions are not readily apparent; analyze information and standard practices to make judgement calls

Your Profile:

  • 4+ years of clinical data management experience in a clinical research organization or pharmaceutical company 

  • Experience leading multiple projects simultaneously 

  • Experience with all steps within the data science lifecycle and most major data science study tasks, with proficiency in at least one Clinical Data Management system required (e.g., Medidata Rave, Inform, Oracle Clinical, Veeva)

  • Excellent communication skills 

  • Timeline management experience 

  • Data Analytic and Data Validation experience

  • Bachelor’s degree or local equivalent 

  • Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated above. All employees must read, write, and speak fluent English and host country language

*Please, submit your CV and application in English

#LI-Hybrid

#LI-DT2

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 maximize 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 site to read more about the benefits ICON offers.

At 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, color, 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.

Are you a current ICON Employee? Please click here to apply

Top Skills

Inform
Medidata Rave
Oracle Clinical
Veeva
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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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