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Principal Statistical Programmer

Syneos Health

Posted this week

LOCATION

IND · Remote

EXPERIENCE

8+ Years

TYPE

FullTime

SALARY

Negotiable

SKILLS REQUIRED

eSubmission ReadinessDefine.xml ValidationStatistical Programming SpecificationsTLF Development

Job description

Overview

Principal Statistical Programmer role supporting clinical/SAS/statistical programming for SDTM/ADaM dataset and TLF development, safety/efficacy analyses, and CDISC-compliant e-submissions.

What you'll do

Develop and validate SDTM/ADaM datasets and TLFs.
Prepare specifications and generate Define.XML, ADRG, and SDRG.
Support safety and efficacy analyses.
Contribute to e-submissions and ensure CDISC compliance.
Collaborate with cross-functional teams across studies and lead clinical study trials.
Work across therapeutic areas including Oncology, Neurology, or any TA.

What you'll need

8+ years of relevant clinical/SAS/statistical programming experience.
Lead experience of min 1+ year.
Excellent understanding of the clinical domain and CDISC standards.
Experience across various supported therapeutic areas.
Strong communication and problem-solving skills.
Ability to work collaboratively in cross-functional teams in a dynamic environment.

Details

Location: IND-Remote.

Read the full description and apply on the company’s own careers page.

Hiring on Abekus is free for applicants

We never charge a fee, and employers are prohibited from doing so. If a recruiter asks for payment, please report them right away.

Principal Statistical Programmer

Syneos Health

Posted this week

LOCATION

IND · Remote

EXPERIENCE

8+ Years

TYPE

FullTime

SALARY

Negotiable

SKILLS REQUIRED

eSubmission ReadinessDefine.xml ValidationStatistical Programming SpecificationsTLF Development

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Job description

Overview

Principal Statistical Programmer role supporting clinical/SAS/statistical programming for SDTM/ADaM dataset and TLF development, safety/efficacy analyses, and CDISC-compliant e-submissions.

What you'll do

Develop and validate SDTM/ADaM datasets and TLFs.
Prepare specifications and generate Define.XML, ADRG, and SDRG.
Support safety and efficacy analyses.
Contribute to e-submissions and ensure CDISC compliance.
Collaborate with cross-functional teams across studies and lead clinical study trials.
Work across therapeutic areas including Oncology, Neurology, or any TA.

What you'll need

8+ years of relevant clinical/SAS/statistical programming experience.
Lead experience of min 1+ year.
Excellent understanding of the clinical domain and CDISC standards.
Experience across various supported therapeutic areas.
Strong communication and problem-solving skills.
Ability to work collaboratively in cross-functional teams in a dynamic environment.

Details

Location: IND-Remote.

Read the full description and apply on the company’s own careers page.

Hiring on Abekus is free for applicants

We never charge a fee, and employers are prohibited from doing so. If a recruiter asks for payment, please report them right away.

Principal Statistical Programmer

Principal Statistical Programmer

Job description

Principal Statistical Programmer

Get certified in what this role needs

Job description

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