About the role
Senior Statistical Programmer
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
Join a sponsor-dedicated team, progressing with in-house study activities over the years. Experienced SAS programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs.
What You Will Do
- Data preparation and cleaning: Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for PK/PD analysis.
- Programming PK/PD analyses: Writing SAS code to perform descriptive analysis of PK/PD data and statistical analysis of exposure-response relationships.
- Data visualization: Creating clear and informative graphs and tables to effectively communicate PK/PD findings.
- CDISC compliance: Ensuring data is formatted according to CDISC standards for regulatory submissions
- Validation and quality control: Performing thorough validation checks on programming code and analysis results to maintain data integrity.
- Identifies problems and develops tools that increase the efficiency and capacity of the Clinical PK/PD Programming group.
- Provide trainings to fellow programmers on industrial guidance, new or enhanced features of software tools that are relevant or applicable to job function above.
- Your Profile: Bachelor’s degree in Math, Stats, Computer Science or similar
- 7+ years of industrial experience
- Must have advanced SAS programming skills, with knowledge of other statistical software like R being beneficial.
- Knowledge of CDISC standards (SEND, SDTM, and ADaM) is required.
- Desire to work in clinical PK/PD – knowledge and experience of PK/PD concepts and related programming is highly desirable.
- Experience visualizing/presenting data for internal stakeholders or clients
- Capable of implementing more advanced modeling and statistical procedures as requested by study team.
- Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis, and reporting/modeling of analysis results. Including handling of data issues and uncleaned data.
- Professional attitude, self-motivated, logical thinking
Excellent attention to detail
- Strong organization skills and ability to work on multiple tasks simultaneously while achieving quality standards and meeting deadlines
- Good verbal and written communication skills. Strong interpersonal skills and ability to work collaboratively across teams
- Ability to problem solve and develop innovative approaches along with a drive to learn and master new techniques and technologies.
- 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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- Are you a current ICON Employee? Please click here to apply