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Senior Clinical Data Science Lead

5+ years
Not Disclosed
10 April 23, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Clinical Data Science Lead

About ICON plc: ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, government, and public health organizations. With patients at the center of all we do, our mission is to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, driving our success through their mission to succeed and passion for excellence.

Services Overview:

  • Clinical Data Management Expertise with scientific review of complex clinical data in collaboration with Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS).

What You Will Be Doing:

  • Perform scientific clinical data reviews with a focus on complex indications and therapy-related study elements.

  • Participate in study-related activities from protocol design onwards, providing input on data collection tools.

  • Partner closely with study physicians and study scientists to establish, align, and confirm clinical data review expectations for assigned trials.

  • Review content and integration requirements for eCRFs and other data collection tools.

  • Review complex scientific study data, manage queries, and collaborate with relevant stakeholders.

  • Participate in other review activities, such as coding and SAE reconciliation, as needed.

  • Lead and attend study-related meetings as appropriate.

  • Establish conventions and quality expectations for clinical data.

  • Collaborate with study physicians, scientists, global data managers, statisticians, and other stakeholders.

  • Identify and communicate lessons learned and best practices.

Qualifications:

  • Bachelor’s degree or higher, preferably in a health or scientific discipline.

  • 5+ years of Clinical Data Management experience.

  • Robust experience with EDC systems (e.g., Medidata Rave) and data review tools such as J-Review.

  • Deep understanding of drug development processes.

  • Strong technical skills with advanced proficiency in Microsoft Excel.

  • Excellent written and oral communication skills.

What ICON Can Offer You:

  • Competitive salary with a range of additional country-specific benefits.

  • Various annual leave entitlements.

  • Health insurance options tailored to your needs and your family's.

  • Competitive retirement planning support.

  • Access to a Global Employee Assistance Programme (TELUS Health) offering 24-hour support.

  • Life assurance coverage.

  • Flexible benefits including childcare vouchers, bike purchase schemes, gym memberships, subsidized travel passes, and health assessments.

Diversity and Inclusion: At ICON, inclusion and belonging are fundamental to our culture and values. We are committed to creating an inclusive and accessible environment, providing equal employment opportunities regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Reasonable accommodations are available upon request during the application process.

For more information on ICON’s benefits, visit: ICON Careers Benefits
For reasonable accommodation requests, visit: ICON Accommodations