#766-Sr Principal Statistical Programmer-Remote(Permanent role)

ClinChoice; Chicago (IL); Remote; USD 120,000 - 160,000; Full time

Job summary

A leading global full-service CRO seeks a Sr Principal Statistical Programmer for their Chicago office. This permanent role requires extensive experience in clinical programming and offers an opportunity to lead projects within a collaborative team dynamic. The successful candidate will enjoy a fulfilling career, contributing to innovative drug development within a supportive environment that values professional growth.

Qualifications

• 10+ years clinical programming experience or 9+ years with a Master's degree.
• Good knowledge of ICH and Good Clinical Practices.
• Strong communication and leadership skills essential.

Responsibilities

• Programming edit checks with SAS and creating clinical reports.
• Coordinating projects and managing Programming groups.
• Mentoring team members and ensuring compliance with industry standards.

Skills

Programming

Data Management

Leadership

Communication

Detail-oriented

Education

Bachelor's degree in computer science, statistics or related disciplines

Master's degree in computer science, statistics or related disciplines

Job description

#766-Sr Principal Statistical Programmer-Remote(Permanent role)

Join to apply for the #766-Sr Principal Statistical Programmer-Remote(Permanent role) role at ClinChoice

#766-Sr Principal Statistical Programmer-Remote(Permanent role)

1 day ago Be among the first 25 applicants

Join to apply for the #766-Sr Principal Statistical Programmer-Remote(Permanent role) role at ClinChoice

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture. We are looking for a dynamic person to join our in-house team as a Sr Principal Statistical Programmer on a permanent basis.

Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career!

Responsibilities

Key responsibilities and skills may include, but are not limited to:

• Programming edit checks for Data Management with SAS.
• Create tables, listings and figures for clinical study report.
• Independently annotated blank CRF (acrf.pdf) with appropriate tools per FDA or CDISC guidelines.
• Create or QC SDTM specifications and SDTM datasets.
• Create or QC ADaM specifications and ADaM datasets.
• Create or QC define.xml or define.pdf
• Create Study Data Reviewer's Guide (cSDRG.pdf) and Analysis Data Reviewer's Guide (ADRG.pdf)
• Serve as team leader for one/more Programming groups.
• Independently coordinate and manage the preparation, execution, reporting and documentation of projects within a Programming group.
• Manage and coordinate the integration of data across studies in support if ISS and ISE and electronic submission deliverables.
• Following industry standards and be a mentor to other Programming leads or managers.
• Manage programming team. Take initiatives and follow through to develop the Programming team. Dare to lead.
• Be a role model for team members.
  
  

Qualifications

• Bachelor's degree in computer science, statistics or related scientific disciplines with 10+ year clinical programming experience; Master's degree in computer science, statistics or related disciplines with 9+ year of clinical programming experience;
• Working knowledge of ICH, Good Clinical Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology
• Good understanding of clinical drug development process
• Detail oriented
• Strong communication skills and coordination skills
• Good leadership skills
  
  

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.

Who will you be working for?

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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at ClinChoice by 2x

Get notified about new Senior Statistical Programmer jobs in Chicago, IL.

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.