SDTM Programmer I

Pharmaceutical Research Associates, Inc; United Kingdom; Remote; GBP 45,000 - 75,000; Full time

Job summary

Join a forward-thinking organization as a Clinical Database Programmer, where your expertise in SAS programming will play a pivotal role in transforming clinical data into actionable insights. In this dynamic position, you will extract and analyze clinical data, ensuring its accuracy and compliance with regulatory standards. Collaborate with a diverse team to enhance programming efficiency and contribute to the success of groundbreaking clinical studies. Enjoy a supportive work environment that values your contributions and offers a comprehensive benefits package focused on well-being and work-life balance. If you're passionate about making a difference in the pharmaceutical industry, this opportunity is for you.

Benefits

Annual Leave Entitlements

Health Insurance Options

Retirement Planning Options

Employee Assistance Programme

Life Assurance

Gym Discounts

Travel Passes

Qualifications

• 5+ years of clinical SAS programming experience in the pharmaceutical industry.
• Strong knowledge of CDISC SDTM mapping and data transfer operations.

Responsibilities

• Extract clinical data and produce reports primarily in SAS.
• Perform programming to convert raw clinical trial data to SDTM format.

Skills

SAS Programming

CDISC SDTM Mapping

Data Quality Control

Communication Skills

Education

Bachelor's Degree

Certification in Clinical Research

Tools

SAS

eCRF

eCRT

Job description

Overview

As a Clinical Database Programmer, you will join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

What you will be doing:

• Extract clinical data from the clinical data management system and produce standard and custom reports, primarily in SAS.
• Program reports and listings as requested by project team members for ongoing studies.
• Develop transfer specifications with vendors for external data sources.
• Perform consistency checks on data transferred between stakeholders and external parties to ensure completeness and accuracy of data transfers.
• Perform programming to convert raw, clinical trial data to Study Data Tabulation Model (SDTM) format.
• Perform Quality Control (QC) on programming work performed by fellow Database Programmers.
• Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency.

Qualifications

You are:

• Bachelor’s degree OR certification.
• Minimum of 5 years of clinical SAS programming experience in the pharmaceutical industry.
• Working knowledge of CDISC SDTM mapping, specifications, conversion, domains, datasets, eCRF, eCRT.
• Experience with Package/define.xml development and SDTM data transfer operations on clinical studies.
• Understanding of regulatory requirements relevant to submissions.
• Knowledge of clinical trial study design and electronic data submission requirements.
• Strong communication and interpersonal skills, with the ability to work effectively as part of a team.

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we prioritize building a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• A range of health insurance options for you and your family
• Competitive retirement planning options
• Global Employee Assistance Programme, TELUS Health, with 24-hour access to a network of over 80,000 professionals
• Life assurance
• Flexible, country-specific benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, and health assessments

Visit our careers website to learn more about working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture. We are committed to providing an inclusive, accessible environment and a workplace free of discrimination. Qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need a reasonable accommodation during the application process or to perform the job, please let us know through the provided form: https://careers.iconplc.com/reasonable-accommodations

We encourage you to apply even if you don’t meet all the requirements—your skills and potential might be a perfect fit.

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