PK/PD Statistical Programmer

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.

• 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

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.