Clinical Programming – Contractor – SDTM & DO

SGS_JOB_3650

Business Support
Remote
SAS
SDTM datasets
eSUB

Contract - 02 Year Contract

Position Summary: The Clinical Programming (Contractor) is responsible for providing comprehensive programming support, including managing the timely and accurate execution of programming components of clinical trials. The clinical programming contractor independently manages completed projects that involve global tasks, or cross functional teams The role may require providing inputs to design of CRFs, Data Transfer specifications, creation of SDTM specifications and datasets, and reporting the results of clinical trials, including programming rules and electronic submissions for Client`s products. 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.

Job Responsibilities:

  • Primarily works at the Study, product / program level
  • Provides comprehensive programming support, including development of programs, SDTM specifications, SDTM datasets complying with regulatory requirements, departmental SOPs and work practices, including generation of data review and operational listings and reports.
  • Manages and Delivers assignments with good quality and within timelines
  • Provides programming support to CDISC based e-submission. Develop, debug, and enhance SAS programs to support quality control of SDTM datasets and Define packages.
  • 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.
  • Responsible for performing data handling activities on an ongoing basis to ensure accuracy, reliability, integrity, consistency and completeness of the data prior to database lock and providing the final data to clinical programming and statistics during various study milestones.
  • Responsible to support creation of case report forms (CRFs) and specifications in accordance with SDTM guideline and Client standards, including defining external (non-CRF) and support the functional review and approval process.
  • Proactively communicates issues impacting programming deliverables with Stat or DM team members.

Skills:

  • Experience Required: • Bachelors + 5 year, Masters + 4 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, database concepts used in clinical trials.
  • Strong understanding of SDTM standards and Implementation guides.
  • Demonstrated proficiency in using SAS to produce study SDTM datasets, eSUB components and using other software applications (eg. Pinnacle 21, XML and MS Office)
  • Demonstrated ability to work independently and in a team environment.

Education/Experience:

  • Education Required: Bachelor’s Degree/Master’s Degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
  • 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 SDTM datasets and associated documents/specifications in study/project.
  • Have solid knowledge of Clinical data, SDTM IG and Pinnacle 21.
  • Company/Industry Related Knowledge: Advanced knowledge of government regulations (such as CDISC and ICH) pertaining to drug development in multiple therapeutic areas.

Related Jobs

Probabilistic Safety Analysis Engineer III- New Nuclear

Business Support
 Washington
12 Months

Location : Richland, WA, 99354 A Probabilistic Safety Analysis (PSA) Engineer works on evaluating and improving the safety of nuclear power systems using risk-based methods. The role involves analyzing potential hazards, supporting reactor design and construction, ensuring compliance with regulatory standards, and contributing to the safe operation of advanced nuclear technologies

Probabilistic
Nuclear
Safety

Probabilistic Safety Analysis Engineer I- New Nuclear

Business Support
 Washington
12 Months

Location : Richland, WA, 99354 A Probabilistic Safety Analysis (PSA) Engineer works on evaluating and improving the safety of nuclear power systems using risk-based methods. The role involves analyzing potential hazards, supporting reactor design and construction, ensuring compliance with regulatory standards, and contributing to the safe operation of advanced nuclear technologies

Probabilistic
Nuclear
Safety

TECHNICAL WRITER II

Business Support
 Illinois
9 Months

Location : WARRENVILLE Illinois 60555 We are seeking a meticulous and detail-oriented Technical Writer to join our team. In this role, you will be responsible for developing, writing, and editing comprehensive supply policies and procedures. You will work closely with various departments within and outside of Supply to ensure all documentation is accurate, clear, and accessible, supporting the efficient operation of our supply chain processes

Technical
Writing
Supply

Training Specialist Sr

Business Support
 Pennsylvania
12 Months

A Senior Training Specialist designs and develops effective learning programs and training materials for employees. The role focuses on creating engaging eLearning and instructor-led content using structured instructional design methodologies to enhance workforce skills and performance

ADDIE
Articulate

BUSINESS ANALYST I

Business Support
 Texas
12 Months

Location : Houston Texas 77002 A Data Entry Analyst is responsible for accurately processing high volumes of customer payment data within internal systems. This role focuses on maintaining precision and consistency in repetitive, process-driven tasks while ensuring correct payment application and data integrity.

Data Entry
Payment
Excel

Phlebotomist

Business Support
 Florida
12Months + (highest possibilities of contract extension)

Location: 3340 Enterprise Way Miramar FL USA 33025 Training Schedule: Training is up to 3 months. This is usually 3 days a week onsite from 6:30am – 3:00pm. Once they complete training, the working hours will fluctuate from 0 hours a week up to 40 hours a week. The associates fill out a form listing the days and hours they can work and the client will schedule as needed. The client cannot guarantee the days and number of hours they might work. Many of the workers have more then 1 job and they are able to fit Teva into their working schedules.

study protocol
Good Clinical Practice standards
Standard Operating

Licensing Engineer II - Engineering Projects

Business Support
 Washington
12 Months

A Licensing Engineer provides regulatory and technical support to ensure nuclear engineering projects comply with government and industry requirements. The role focuses on coordinating with internal teams and regulatory bodies, supporting licensing processes, and ensuring environmental and safety standards are met for nuclear facilities

Licensing
Regulatory

Licensing Engineer - Engineering Projects

Business Support
 Washington
12 Months

A Licensing Engineer provides regulatory and technical support to ensure nuclear engineering projects comply with government and industry requirements. The role focuses on coordinating with internal teams and regulatory bodies, supporting licensing processes, and ensuring environmental and safety standards are met for nuclear facilities

Licensing
Regulatory

Product Marketing Manager, TESTING Bioprocessing

Business Support
 Maryland
6 Months

A Product Marketing Manager in bioprocessing is responsible for developing and executing marketing strategies for life science products. This role bridges science and business by translating complex bioprocessing solutions into clear value propositions, driving product adoption, and supporting sales growth in global markets

Product
Marketing
logo

At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.


© 2026 All rights reserved.
logologologologo