Statistical Programming Contractor 3
Aequor JD ·www.aequor.com
Apply directPositions 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: • Expert level of programming skills and problem resolution in SAS.
• Expert level of knowledge in CDISC based e-submission (creation of ADaM datasets and associated TLGs in study/project (e.g. ISS/Client), creation of Bioresearch Monitoring (BIMO) Inspection deliverables).
• Have solid knowledge of statistical models used for efficacy data analysis.
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
2. Influences communication toward common understanding and actionable results;
3. Good oral and written communication skills.
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: • Expert level of programming skills and problem resolution in SAS.
• Expert level of knowledge in CDISC based e-submission (creation of ADaM datasets and associated TLGs in study/project (e.g. ISS/Client), creation of Bioresearch Monitoring (BIMO) Inspection deliverables).
• Have solid knowledge of statistical models used for efficacy data analysis.
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
2. Influences communication toward common understanding and actionable results;
3. Good oral and written communication skills.
Frequently asked questions
Who is hiring for the Statistical Programming Contractor 3 role?
Aequor JD is hiring for the Statistical Programming Contractor 3 position, a Shazamme client. Apply directly on the employer's career site.
Where is the Statistical Programming Contractor 3 job located?
The Statistical Programming Contractor 3 role with Aequor JD is based in Piscataway, NJ, US. The role is remote-friendly.
Is the Statistical Programming Contractor 3 role remote?
Yes — the Statistical Programming Contractor 3 position at Aequor JD is remote. Candidates based in US are preferred.
What does the Statistical Programming Contractor 3 role pay?
Aequor JD lists the Statistical Programming Contractor 3 role at USD 62–71 per hour.
Is the Statistical Programming Contractor 3 role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the Statistical Programming Contractor 3 role?
The Statistical Programming Contractor 3 position is aimed at mid-level candidates.
How do I apply for the Statistical Programming Contractor 3 role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.