Statistical Programming Contractor 3

Positions Requested : 4 U.S. - Based opportunities

Projected Start Date : 1 for September 2025, 1 for October and 2 for November.

Assignment Duration : Up to two years

Does the position allow for the worker to be virtual / remote? 100% Remote role - US Based Candidate

Shift Schedule : Morning - US time zone 8 hours / day

Core essential skill sets candidates must have to be considered for the role :

1. Expert level of programming skills and problem resolution in SAS.

2. Advanced knowledge of government regulations (such as CDISC and ICH guidelines) pertaining to drug development in multiple therapeutic areas.

3. Tackles difficult problems; Identifies solutions and help leading decisions to resolve

Manage and deliver assignments with quality and within timelines by being independ and proactive

4. Solid Statistical Knowledge

Position Summary :

The Statistical Programming Contractor 3 is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials.

The statistical programming contractor independently manages completed projects that involve global tasks, or cross functional teams The role may require providing inputs to design and analysis, and reporting the results of clinical trials, including programming rules and mocked T / L / G. In addition, providing programming support for publication for our marketed drugs.

Travel Requirements : N / A

Essential Duties & Responsibilities :

1. Primarily works at the study, product / program level

2. Provides comprehensive programming support, including development of programs, ADaM specifications, analysis (datasets, TLGs) complying with regulatory requirements, departmental SOPs and work practices.

3. Manages and Delivers assignments with good quality and within timelines

4. Provides programming support to CDISC based e-submission. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets and TLGs.

5. Implement programming standards and comply with regulatory requirements among project team members and across all projects; communicate to management on project status and resource gaps.

6. Responsible for the standardization of GSD deliverables (datasets and associated TLGs) across study projects within an indication / therapeutic area. Provides input on opportunities for process improvement

7. Proactively communicates issues impacting programming deliverables with Stat or DM team members.

Position Requirements :

Education Required : Bachelor's Degree / Master's Degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.

Experience Required :

• Bachelors + 7 year, Masters + 6 years of professional experience in a pharmaceutical or clinical research setting as a programmer.
• Proficient knowledge of clinical trials and drug development process, industry standards, statistical concepts used in analysis and submissions of clinical trial data.
• Strong understanding of SDTM, ADaM standards and Implementation guides.
• Demonstrated proficiency in using SAS to produce analysis datasets, TLGs, eSUB components and using other software applications (eg. Pinnacle 21, XML and MS Office)
• Demonstrated ability to work independently and in a team environment.

Experience Preferred :

Specialized or Technical Knowledge Licenses, Certifications needed :

Functional Knowledge :

Company / Industry Related Knowledge : Advanced knowledge of government regulations (such as CDISC and ICH) pertaining to drug development in multiple therapeutic areas.

Job-Specific Competencies :

1 Tackles difficult problems; identifies solutions and recommends action management

3. Good oral and written communication skills.