Clinchoice Inc.
Senior Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)
United States · Senior
Stay score
odds of building a lasting career here
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
Personalize to your clock →Employer immigration record
from this employer's Department of Labor filings
Green-card filing pattern in this occupation
Green-card follow-through: 90%
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
Community outcomes
No reports yet — be the first to help the next applicant.
About the role
- 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 in.
Responsibilities
- Ability to work independently and manage multiple priorities in a fast-paced environment
- Develop, validate, and maintain SAS programs for clinical study data analysis and reporting
- Collaborate with Biostatistics, Data Management, and Clinical teams
- Participate in study planning, review specifications, and support submission activities
- The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project.
- This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks
- Create datasets, tables, listings, and figures according to study requirements
- 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.
Requirements
- Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience
- Master's degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience.
- Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
- Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Nice to have
- Experience supporting regulatory submissions is preferred
Benefits
- Education and Experience:
- ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.
Company info
- 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.
- Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
Visa & Work Authorization
- 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?
This listing is sourced directly from Clinchoice Inc.'s careers page and normalized into a canonical job model.