About the role

Aplyr's Quick Take

This role is for a Senior Clinical Data Science Programmer focused on developing and maintaining clinical study listings using SAS. You'll work remotely, managing listings for clinical trials and collaborating with stakeholders to ensure quality and compliance. It's an individual contributor role that requires technical expertise in clinical data programming.

Good fit

Ideal candidates have at least 3 years of experience in clinical data programming, particularly with SAS, and a background in life sciences or statistics. Strong communication skills and the ability to work independently in a remote setting are essential.

Worth noting

The position is fully remote, which offers flexibility, but it also involves direct client interaction, so strong interpersonal skills are crucial. The emphasis on compliance and quality control may indicate a high-pressure environment.

Senior Clinical Data Science Programmer (Clinical SAS Listings)

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.

Are you an experienced Clinical SAS Listings Programmer with 3+ years of experience developing and maintaining clinical study listings looking for your next opportunity?

ICON is growing and we're looking for talented professionals to join our Clinical Data Science team in a fully remote role. This is an exciting opportunity for an experienced programmer with strong expertise in Clinical Study Listings, including DM Listings and Reconciliation Listings, to work in a client-facing role and deliver high-quality clinical data science and programming solutions that support clinical development programmes across a global portfolio.

What You Will Be Doing

Develop, validate, and maintain Clinical Study Listings, including DM Listings, Reconciliation Listings, and other study-specific listings.
Ensure study listings are configured, delivered, and maintained in line with agreed timelines and quality expectations.
Manage clinical study listings in compliance with clinical standards to support the successful execution of clinical trials.
Serve as the subject matter expert for Clinical Study Listings, providing support, troubleshooting, and maintenance activities.
Partner directly with stakeholders, providing technical expertise and acting as a key contact for programming-related activities.
Participate in client meetings, delivering updates, presenting outputs, and supporting decision-making throughout the study lifecycle.
Provide guidance on programming best practices, coding standards, validation approaches, and data quality controls.

You Will Have/Be

Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related discipline.
Minimum 3 years of experience developing, validating, and maintaining Clinical SAS Listings.
Demonstrated experience producing DM Listings, Reconciliation Listings, and other clinical study listings.
Strong proficiency in SAS and experience with programming languages such as R, Rave Custom Functions, and Python.
Understanding of CDISC standards and clinical reporting best practices.
Excellent verbal and written communication skills.
Ability to work independently in a remote environment while managing multiple priorities and deadlines.

#LI-RD1

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.

Are you a current ICON Employee? Please click here to apply

Skills & Tags

data

Aplyr's read

ICON plc is a leading global provider of outsourced services in the pharmaceutical industry, attracting professionals in clinical research and data management.
Synthesized from recent postings & public sources

What's promising

•ICON plc has a strong global presence, enhancing its ability to manage international clinical trials effectively.
•The company offers diverse career opportunities across various roles in clinical research and data analysis.
•ICON's focus on innovation in pharmaceutical services supports its competitive edge in the industry.

What to watch

•The pharmaceutical industry is highly regulated, which may limit flexibility in project execution.
•ICON's reliance on large pharmaceutical clients could pose risks if partnerships dissolve.
•The competitive nature of the CRO market may pressure ICON to maintain cost efficiency.

Why ICON plc

•ICON plc specializes in comprehensive outsourcing solutions, differentiating it from competitors with narrower service scopes.
•The company's integration of technology in clinical trials offers a unique advantage in data management.
•ICON's strategic acquisitions have expanded its capabilities and market reach significantly.

Aplyr’s read is generated by AI from public sources. Was it useful?

About ICON plc

ICON plc

iconplc.com

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ICON plc is a global provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology, and medical device industries.