You will manage day-to-day clinical data science activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
Lead the development of Data Transfer Specifications (DTS) documents to align external data providers and research partners on the required structure for new data. This includes:
Authoring the DTS, responding to external data providers and internal stakeholder queries to ensure
data will be delivered in the correct format and structure.
Track DTS status with external data providers across different data types and programs and ensure data completion dates are met for study timelines and deliverables.
Ensuring data structure based on the type(s) of data being used is consistent and compliant with appropriate data templates.
Ensuring data structure is consistent across each data provider and comply with appropriate data templates.
Support data reconciliation and data structure inquiry resolution.
Liaise cross functionally to facilitate the creation of new test codes.
Participate in the Clinical Study Team as an extended team member.
Oversee and train in the use of the DTS and other supplemental documents.
Contribute to improvement initiatives as it relates to external data process.
Ensure study teams adhere to CDISC standards as it relates to external data.
Comply with all pertinent regulatory agency requirements (Understand clinical protocols and requirement for Biomarkers/Imaging/eCOA data, blinding and analysis expectations).
Process change requests to update existing DTS.
Improve templates for existing DTS to ensure data harmonization and downstream analytics.
Provide external data management oversight to vendors, providing a pathway for functional discussions, partnership level processes & standards, portfolio status, communication, and escalation.
Review and contribute to eCRF and EDC builds as it relates to external data requirements.
Your Profile:
You will have solid clinical data science experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
Expertise in biomarker data types and/or Imaging data for oncology and non-oncology studies is preferred
Experience working with multiple data types/formats
Experience in managing clinical, biomarker data, eCOA and imaging data
Demonstrates broad knowledge of all applicable regulations including 21 CFR
Part 11, ICH-GCP Guidelines and CDISC standards for data collections.
Demonstrates advanced knowledge of Data Management processes and industry best practices.
Advanced knowledge and experience with extracting data into SAS, CSV, and
XML formats is required.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .
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Benefits
Health insuranceDental insuranceVision insurance
Additional Information
Senior Lead Clinical Data Science Programmer
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior Lead Clinical Data Science Programmer at ICON, you will be instrumental in leading the development and implementation of advanced data science solutions for clinical trials.
Icon · Bangalore, India