Senior Statistical Programmer /Analyst Consultant

ClinChoice; United States; On-site; USD 90,000 - 130,000; Full time

Job summary

ClinChoice is looking for a Senior Statistical Programmer Consultant to work in a hybrid role across NJ, PA, or DE. The ideal candidate will be responsible for programming in clinical trials, validating datasets, and ensuring high-quality deliverables. Candidates should have significant experience in SAS and R programming, alongside a degree in a related field.

The role requires strong analytical skills, communication abilities, and a familiarity with the drug development process. This is an exceptional opportunity to join a leading global CRO known for its employee-focused culture.

Qualifications

• 5+ years in statistical programming with SAS in the pharmaceutical industry.
• Working knowledge of SAS components and R programming.
• Strong knowledge of industry standards and drug development processes.

Responsibilities

• Program and validate datasets, figures, tables for clinical trials.
• Oversee programming deliverables from CROs.
• Ensure programming deliverables meet quality standards.

Skills

SAS programming

R programming

Statistical analysis

Data integration

Oral and written communication

Education

Bachelor or Master in Computer Science, Mathematics, Engineering, Medical or related discipline

Tools

SAS

R

Job description

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

Location: NJ/PA/DE; Hybrid role in any of these location

Job Summary

The contract Senior Statistical Programmer is a member of the Biometrics Department within the Research and Development (R&D) organization who supports Statistical programming work in accordance with corporate standard operating procedures (SOPs), GCP, 21 CFR and ICH guidance.

Responsibilities

Programing for clinical trials

• Program and validate derived datasets, tables, figures, listings. Process data from the external sources.
• Perform ad hoc exploratory analyses for publications and programming support other functions of Research and Development or other organizations.
• Oversee programming work/deliverables from CROs.
• Contribute to the design/implementation/review of Case Report Form, Data Transfer Specification, Statistical Analysis Plan, SDTM/ADaM Specification documents, Define packages.

Electronic submissions

• Program and validate CDISC compliant deliveries for the electronic submissions.
• Support in the creation of supporting documentation for submissions.

Project Management

• Ensure programming deliverables are on time and of high quality.
• Help managing internal contractors and external vendors.

Standards and Guidelines

• Participate in development of departmental working instructions and guidelines.
• Help in creation of enhanced functions/macros and utilities.

Qualification & Experience

• Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline.
• BS with more than 5 or MS with 3 years of experience in statistical programming (SAS, R) in the pharmaceutical industry.
• Working knowledge of SAS and its various components.
• Knowledge of R programming in clinical trials.
• Familiarity of the drug development process.
• Strong SAS and SAS Macro language skills.
• R programming skills in clinical trials.
• Strong knowledge of industry standards.
• Ability to work on data integrations (ISS and ISE).
• Strong oral and written communication skills. Ability to communicate details of the analysis to other team members with less technical experience.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.