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Pk Pd Sas Programmer Jobs (NOW HIRING)

Manager, Clinical Pharmacology

La Jolla, CA · On-site

$106K - $176K/yr

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong written and verbal communication skills PREFERRED QUALIFICATIONS * Experience interpreting PK and PK/PD ...

Manager, Clinical Pharmacology

Bothell, WA · On-site

$106K - $176K/yr

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong written and verbal communication skills PREFERRED QUALIFICATIONS * Experience interpreting PK and PK/PD ...

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong written and verbal communication skills PREFERRED QUALIFICATIONS * Experience interpreting PK and PK/PD ...

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong written and verbal communication skills PREFERRED QUALIFICATIONS * Experience interpreting PK and PK/PD ...

Manager, Clinical Pharmacology

Groton, CT · On-site

$106K - $176K/yr

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong written and verbal communication skills PREFERRED QUALIFICATIONS * Experience interpreting PK and PK/PD ...

Manager, Clinical Pharmacology

La Jolla, CA · On-site

$106K - $176K/yr

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong written and verbal communication skills PREFERRED QUALIFICATIONS * Experience interpreting PK and PK/PD ...

Manager, Clinical Pharmacology

New York, NY · On-site

$106K - $176K/yr

PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD * Strong written and verbal communication skills PREFERRED QUALIFICATIONS * Experience interpreting PK and PK/PD ...

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Pk Pd Sas Programmer information

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$14

$49

$79

How much do pk pd sas programmer jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for pk pd sas programmer in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

What is a PK/PD SAS Programmer?

A PK/PD SAS Programmer is a specialized data analyst who uses SAS software to analyze pharmacokinetic (PK) and pharmacodynamic (PD) data in clinical trials. Their primary role is to process, analyze, and report data related to how drugs are absorbed, distributed, metabolized, and excreted in the body, as well as their biological effects. They collaborate closely with clinical pharmacologists, statisticians, and other researchers to ensure accurate and compliant data analysis. This position is essential in pharmaceutical and biotechnology companies to support drug development and regulatory submissions.

What is the difference between Pk Pd Sas Programmer vs Data Analyst?

AspectPk Pd Sas ProgrammerData Analyst
Required SkillsProficiency in SAS, programming, data manipulationData analysis, statistical skills, SQL
Work EnvironmentHealthcare, finance, pharmaceutical industriesBusiness, marketing, finance sectors
CertificationsSAS certifications, programming coursesData analysis certifications, SQL, Excel

The Pk Pd Sas Programmer primarily focuses on developing and maintaining SAS programs for data processing in industries like healthcare and finance. In contrast, Data Analysts interpret data to support business decisions, often using SQL and statistical tools. While both roles require data handling skills, Pk Pd Sas Programmers are more specialized in SAS programming, whereas Data Analysts have broader analytical responsibilities.

How does a PK/PD SAS Programmer typically collaborate with clinical research teams during drug development studies?

A PK/PD SAS Programmer works closely with pharmacokineticists, pharmacodynamic specialists, statisticians, and clinical data managers to analyze and interpret complex clinical trial data. They are responsible for developing and validating SAS programs to support data analysis, ensuring that results are accurate and compliant with regulatory standards. Regular meetings and clear communication with cross-functional teams are crucial, as programmers often need to translate scientific objectives into technical specifications and troubleshoot data or programming issues as studies progress.

What are the key skills and qualifications needed to thrive as a PK/PD SAS Programmer, and why are they important?

To thrive as a PK/PD SAS Programmer, you need a solid background in pharmacokinetics/pharmacodynamics, statistical analysis, and strong programming skills in SAS, usually with a degree in life sciences, statistics, or a related field. Familiarity with clinical trial data standards (like CDISC), advanced SAS procedures, and data visualization tools is typically required. Excellent problem-solving abilities, attention to detail, and clear communication skills help distinguish top performers in this role. These competencies are vital for ensuring accurate data analysis, regulatory compliance, and effective collaboration with multidisciplinary teams in drug development.
Infographic showing various Pk Pd Sas Programmer job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $101,929 per year, or $49 per hour.
Senior Clinical Systems Programmer (JReview), Data Operations

Senior Clinical Systems Programmer (JReview), Data Operations

Integrated Resources INC

Woodcliff Lake, NJ

Full-time

Posted 5 days ago


Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Accountable for setting up studies & developing standard programs to create reports, listings, graphs, metrics for clinical data management and other areas of clinical for data review and data cleaning to conduct clinical trials in Oncology area within JReview environment. Develop standard programs for patient profiles, standard and ad-hoc reports for data review using JReview & SAS to support the clinical teams. Design and develop macros, applications, and other utilities to expedite JReview/SAS programming activities.
Develop standard / ad-hoc JReview /SAS programs to provide complex listings/reports to support Data Management and clinical functions to clean and review data for Oncology trials.
Set up studies in JReview, develop & maintain programs, support users, and provide training for JReview.
Develop programs to provide metrics, graphs, patient profiles and ad-hoc reports for data review to support the clinical teams.
Design and develop macros, applications, and other utilities to expedite programming activities and usage by the Oncology Data Management and other areas of Clinical for data review.
Develop and maintain the programs with proper documentation and testing using departmental standards.
Ensure all programming activities and processes performed are conducted according to standard operating procedures and good programming practice.

Qualifications

Strong SAS programming skills in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SAS/AF, SQL;
Strong JReview skills in terms of program development, administration, maintenance, and user support;
Extensive experience of handling external data, e.g., laboratory data, PK, ECG,Tumor, etc.;
Knowledge of developing reporting or other applications using SAS;
Knowledge of data management process; Good understanding of data cleaning process;
Good understanding of standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG;
Good understanding of relational databases, e.g., ORACLE; Knowledge of the EDC System, InForm and underlying data structure is a plus;
Strong problem-solving skills;
Able to work independently and a team player; Good organizational and time management skills ;
Capable of communicating technical concepts
Good understanding of system development life cycles, GCP, and related Regulatory guidelines.

Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus!! Thank you for your time and for consideration. I look forward to hearing from you.

Regards,

Jasmine Jogewar

Sr. Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

(Direct) 732-844-8720| (F) 732-549-5549

www.irionline.com , www.linkedin.com/in/Jasmine-Jogewar



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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996