Principal Statistical Programmer, Early Phase

IQVIA; Durham (NC); Remote; USD 106,000 - 218,000; Full time

Job summary

A leading global provider in clinical research is seeking a Principal Statistical Programmer. This role offers the chance to work in a dynamic environment, providing statistical programming expertise for early phase translation medicine. The position is home-based and requires strong SAS skills, CDISC knowledge, and a Bachelor’s degree in a related field with significant experience. Join a passionate team dedicated to advancing medicine and reshaping healthcare.

Qualifications

• 10+ years of relevant experience in statistical programming.
• Experience with Phase I studies and PKPD data.

Responsibilities

• Provide hands-on statistical programming expertise for early phase translation medicine.
• Create ADaM safety datasets and PK non-compartmental tables.

Skills

SAS

CDISC

Education

Bachelor’s Degree in Statistics

Bachelor’s Degree in Computer Sciences

Bachelor’s Degree in Bioinformatics

Tools

NONMEM

Job description

**Principal Statistical Programmer**

**Location**: Home-based anywhere in the United States or Canada

**Why IQVIA**

Data Sciences Staffing Solutions (DSSS or DS3) is a unit within IQVIA that provides dedicated resources through a Functional Service Provider (FSP) partnership. This allows you to work within a sponsor environment while enjoying the benefits of an industry-leading CRO, utilizing sponsor systems, and being part of a passionate team dedicated to advancing medicine and reshaping healthcare. Your role will be both challenging and rewarding, making a real impact.

Experience the best of both worlds and become a core part of our dynamic team today!

**Job Responsibilities:**

1. Provide hands-on statistical programming expertise for the client’s early phase translation medicine group.
2. Create ADaM safety datasets such as ADSL, ADLB, ADVS, ADEX, ADPC (concentration), ADPP (parameter), and POPPK (NONMEM) datasets, as well as PK non-compartmental (NCA) tables, figures, and listings (TFLs).
3. Experience with Phase I studies, exposure response analysis, crossover design, and pooling of PK parameters is required.
4. Demonstrate strong SAS technical skills and in-depth CDISC knowledge.
5. Maintain good knowledge of regulatory requirements for submissions.

**Required Experience:**

1. Bachelor’s Degree in Statistics, Computer Sciences, Bioinformatics, or related field, with 10+ years of relevant experience.
2. Recent experience working on Phase I studies, specifically with PKPD data, including creation of ADPP and ADPC datasets is **_required_**.
3. Hands-on experience creating NONMEM datasets is strongly preferred but candidates with exposure/knowledge of the process and in-depth work in PKPD/Phase 1 studies will be considered.
4. Project or study lead experience is strongly preferred but not mandatory.

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, aiming to 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 without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other protected categories. More information can be found at https://jobs.iqvia.com/eoe.

The potential base pay range for this role, when annualized, is $106,200 to $218,000. Actual offers will vary based on qualifications, experience, location, and schedule. Additional incentives, bonuses, and benefits may be provided.

We value diverse talent with curious minds and a commitment to innovation. Everyone at IQVIA contributes to our shared goal of improving patient lives worldwide. Thank you for your interest in growing your career with us.

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