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Senior/Principal Statistical Programmer, PK/PD

IQVIA

Philadelphia (Philadelphia County)

On-site

USD 106,000 - 218,000

Full time

Yesterday
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Job summary

A leading pharmaceutical/biotech company is seeking a Principal Statistical Programmer specializing in pharmacokinetics and pharmacodynamics. This role involves designing and analyzing clinical trials, requiring strong expertise in statistical programming and collaboration with cross-functional teams. Candidates should have a Master's or Ph.D. in a related field and substantial experience in the industry.

Qualifications

  • Substantial experience in statistical programming within the pharmaceutical or biotech industry.
  • Proven expertise in PK/PD data analysis and interpretation.
  • Detail-oriented with a commitment to producing high-quality deliverables.

Responsibilities

  • Design, execute, and analyze clinical trials to support drug development.
  • Collaborate with scientists, clinical researchers, and biostatisticians.
  • Ensure successful implementation of clinical development programs.

Skills

Statistical programming
PK/PD data analysis
Analytical skills
Problem-solving
Communication skills

Education

Master's or Ph.D. in Biostatistics, Statistics, or related field

Tools

SAS
R

Job description

Work with one of our preferred clients! Our client is a leading pharmaceutical/biotech company dedicated to advancing medical science and improving patient outcomes through the development of innovative therapeutics. Their research-driven organization focuses on discovering, developing, and commercializing novel drugs across various therapeutic areas.

We are seeking a highly skilled and motivated Principal Statistical Programmer with expertise in pharmacokinetics (PK) and pharmacodynamics (PD) to join our dynamic FSP team.

Position Overview:

As a Principal Statistical Programmer with a specialized focus on PK/PD, you will play a pivotal role in the design, execution, and analysis of clinical trials to support the development of our promising drug candidates. Leveraging your extensive knowledge of statistical programming and PK/PD principles, you will collaborate closely with cross-functional teams of scientists, clinical researchers, and biostatisticians to ensure the successful implementation of our clinical development programs.

Qualifications:
  1. Substantial experience in statistical programming using SAS, R, or other relevant programming languages within the pharmaceutical or biotech industry.
  2. Proven expertise in PK/PD data analysis and interpretation, including modeling and simulation.
  3. Solid understanding of clinical trial designs, protocols, and regulatory requirements related to PK/PD endpoints.
  4. Familiarity with industry standards such as CDISC data structures and guidelines for data submissions.
  5. Strong analytical, problem-solving, and communication skills, with the ability to work effectively in cross-functional teams.
  6. Detail-oriented with a commitment to producing high-quality deliverables.
  7. Master's or Ph.D. in Biostatistics, Statistics, or a related field with a strong emphasis on pharmacokinetics (PK) and pharmacodynamics (PD), capable of working within tight timelines.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. More information is available at https://jobs.iqvia.com/eoe.

The potential base pay range for this role, when annualized, is $106,200 - $218,000. The actual offer may vary based on qualifications, experience, location, and schedule (full or part-time). Additional incentive plans, bonuses, and benefits may also be provided.

At IQVIA, we seek diverse talent with curious minds and a relentless commitment to innovation and impact. Everyone contributes to our shared goal of improving patient lives worldwide. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

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