R&D Programmer III
R&D Programmer III
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Job Description
Start Date: October 2025
Pay: Confidential - Confidential/hr based on experience
Bill: Confidential - Confidential/hr based on experience
Shift Schedule: Morning - US time zone 8 hours/day
Temp to Perm: No - any consideration to convert to FTE will be communicated to Kelly OCG based on business needs
Core essential:
1. Expert level of programming skills and problem resolution in SAS.
2. Strong knowledge of Adam (all apecs-related)
3. Submission experience (required)
4. Advanced knowledge of government regulations (such as CDISC and ICH guidelines)
5. pertaining to drug development in multiple therapeutic areas.
6. 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
7. Solid Statistical Knowledge
8. 7 years of relevant Pharma experience recommended
Screenings:
1. Basic Background
2. 11 Panel Drug Fentanyl
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/ISE) 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.
Additional Details
- Managers Requested Bill Rate : (No Value)
- Shore Options Available for this Position : Onshore Only
- Critical Position : No
- Is this an IT position : No
- Does the position allow for the worker to be virtual/remote : Yes
- Shift Type : Morning
- White/ Blue Collar Worker : White Collar
- Is this request considered Top Management (Level 3 and up) and management support : No
- Will this position have access to highly sensitive information : Yes
- Will this position have access to sensitive assets (controlled substances narcotics etc.) : No
- Is this a Purchasing/procurement position : No
- Project Code : RS-.1150
Employment Type
Full-time
Key Skills
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