Clinical Data Validation Engineer at ICON plc

Reading, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

12 Jul, 26

Salary

0.0

Posted On

13 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical data validation, Data cleaning, Reporting tools, SQL, SAS, R, Python, CQL, Veeva CDB, JReview, Elluminate, CDISC, SDTM, Clinical trial terminology, Data visualization, Metadata Rave

Industry

Biotechnology Research

Description

Clinical Data Validation Engineer 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 Clinical Data Validation Engineer to join our diverse and dynamic team. As a Clinical Data Validation Engineer at ICON, you will work on Clinical Trial Reporting activities delivering listings and visualizations to support Clinical Trials. In addition, you will operate in compliance with Client SOPs and processes. What You Will Be Doing: Create data cleaning reporting solutions with appropriate oversight that support the quality and timely delivery of data cleaning, study status metric, and monitoring reports and visualizations required per standard and study specific data review plans. Create any documentation needed for reports throughout the lifespan of the study and/or asset for all deliverables. Develop a library of reusable checks working closely with data engineers and config specialists. Collaborate with cross functional teams in creating business rules and automated check library across TAU. Complies with applicable SOPs and work practices. Serves as a technical resource for creating data analytics to help with data validation and cleaning. Supports knowledge development of others on reporting tools that support the accuracy and integrity of study data. Provide programming expertise for data cleaning to efficiently ensure high quality data. Enhances available reporting tools/macros/libraries or creates new ones to support the and review of clinical trial data and trial status information for cross-functional use and provides input on data management reporting standards as required. Creates and tests listings for data review. Ensure operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan, in collaboration with the Clinical Data Management and medical reviewers. Your Profile: Bachelor's degree in computer science, statistics, biostatistics, mathematics, biology or other health related field or equivalent experience that provides the skills and knowledge necessary to perform the job. Knowledge of drug development process. Understanding regulatory requirements and relevant data standards; CDISC and SDTM knowledge and experience are preferable. Minimum 2 years’ experience in programming listings and/or visualizations with any of the following Veeva CDB, JReview and Elluminate Hands-on experience with report development in Elluminate preferred. Experience with one of these languages: CQL, SQL, SAS, R, Python Knowledge of clinical database systems (Metadata Rave, Veeva, InForm). Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.) Strong working knowledge of clinical trial terminology Must be able to work in a fast-paced environment. Ability to work independently, take initiative and complete tasks to deadlines. 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 ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

Responsibilities

The Clinical Data Validation Engineer will create data cleaning reporting solutions and visualizations to support clinical trial activities. They will also develop reusable check libraries and provide programming expertise to ensure the accuracy and integrity of clinical trial data.