1019# Principal Statistical Programmer/Analyst Consultant

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  Principal Statistical Programmer/Analyst Consultant  on a contract 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 9+ year clinical programming experience; Master’s degree in computer science, statistics or related disciplines with 8+ 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.           

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