ICON plc

PK/PD Statistical Programmer

ICON plc$110K — $130K *
US-AnywhereRemote in Blue Bell, PA
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor’s degree in Math, Stats, Computer Science, or similar
  • 7+ years of industrial experience
  • Advanced SAS programming skills; knowledge of R is beneficial
  • Knowledge of CDISC standards (SEND, SDTM, ADaM) is required
  • Desire to work in clinical PK/PD with relevant experience
  • Experience visualizing/presenting data for stakeholders
  • Strong understanding of clinical trial data and data manipulation

Responsibilities

  • Clean and transform raw clinical trial data for PK/PD analysis
  • Write SAS code for descriptive analysis of PK/PD data
  • Create graphs and tables to communicate PK/PD findings
  • Ensure data compliance with CDISC standards for regulatory submissions
  • Perform validation checks on programming code and analysis results
  • Identify problems and develop tools to enhance programming efficiency
  • Provide training on software tools and industry guidance for programmers

Benefits

  • Competitive and comprehensive total rewards package
  • Health and wellbeing programmes including medical, dental, and vision coverage
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training
Full Job Description
Senior 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.

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 to read more about the benefits ICON offers.

About ICON plc

ICON plc is a global provider of drug development and commercialisation services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development. ICON has approximately 15700 employees in 40 countries. The company was founded in Dublin, Ireland in 1990 and is headquartered in Leopardstown, Dublin. ICON has been publicly traded on the NASDAQ since 1998.
Learn more about ICON plc
Size
39,300 employees
Market Cap
$16.2 billion
Industry
Net Income
$332.3 million
Founded
2017
5 Year Trend
+26.9%
Revenue
$2.7 billion
NASDAQ

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