Clinical Data Validation Engineer

Posted 4 Days Ago
Blue Bell, PA
In-Office
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
The Lead Clinical Data Science Programmer designs and develops programming solutions for clinical trials, ensuring data accuracy through validation and supporting clinical teams with data insights while mentoring junior programmers.
Summary Generated by Built In
Clinical Data Validation Engineer-Remote

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 are currently seeking a Lead Clinical Data Science Programmer to join our diverse and dynamic team. As a Lead Clinical Data Science Programmer at ICON, you will play a key role in designing and developing clinical data solutions, ensuring the efficient handling, analysis, and reporting of complex clinical trial data. You will collaborate with cross-functional teams to drive data-driven insights that support the advancement of cutting-edge therapies and innovative clinical research.

What You Will Be Doing:
  • Leading the design, development, and validation of data science programming solutions for clinical trials.
  • Collaborating with biostatisticians, data managers, and clinical teams to develop data specifications and analysis plans.
  • Programming and validating datasets, tables, listings, and figures (TLFs) according to study requirements.
  • Ensuring the accuracy, consistency, and integrity of clinical data through rigorous quality control and validation checks.
  • Mentoring and guiding junior programmers and providing technical leadership within the data science programming team.
Your Profile:
  • Bachelor’s or advanced degree in computer science, biostatistics, data science, or a related field.
  • Extensive experience in clinical data programming, with proficiency in SAS, R, or other relevant programming languages.
  • In-depth knowledge of clinical trial data structures, CDISC standards (SDTM, ADaM), and regulatory requirements.
  • Strong analytical and problem-solving skills, with a focus on data accuracy and quality.
  • Excellent communication and leadership skills, with the ability to work collaboratively in cross-functional teams and manage multiple projects simultaneously.

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

R
SAS
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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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