Senior/Principal Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)-Remote
- Role
- Unknown
- Experience
- Senior
- Employment
- Contract
Open to GB only. Set where you work from to check your eligibility.
No BS summary
This is a contract consultant role within a CRO (ClinChoice) embedded with a single sponsor, doing statistical programming (SAS) for CVRM therapeutic areas. Requires strong SAS in pharma/CRO, CDISC data expertise, and regulatory submission support. It's a senior-level position with the lead/support programming effort, working under a Programming team leader.
Required skills
Optional skills
Required languages
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 .
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.
Main Job Tasks and Responsibilities:
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
Key Requirement:
Strong SAS programming experience within the pharmaceutical/CRO industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience in generating and validating SDTM, ADaM, and TLFs Good understanding of CDISC standards and clinical trial processes Ability to work independently and manage multiple priorities in a fast-paced environment Experience supporting regulatory submissions is preferred Strong communication and stakeholder management skills
Responsibilities:
Develop, validate, and maintain SAS programs for clinical study data analysis and reporting Create datasets, tables, listings, and figures according to study requirements Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards and project timelines Participate in study planning, review specifications, and support submission activities
Education and Experience:
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. Need to have Respiratory/Immunology TA experience. Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.
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.
#LI-TT1 #LI-Remote #Senior#Contract
What you'll do
- Serving as a matrix delivery expert that is powerful and strategy that extrapolates to portfolio impact; roadmap adoption and be the Scribe for Win
- Keep metrics across projects to complete high-volume mapping execution from cross-tab lines to datasets
- Validate, define and ensure accuracy and proper archival of FDA and clinical data across multiple programs
- Meta-author with inclusion and diversity responsibilities to improve the success of the team
What they require
- Bachelor's degree in computer science + additional Cyber degrees + AECA
- 5 yrs. of clinical programming (CDISC) experience with Bachelor's degree; 6+ yrs. with Master's degree
- Experience in generating and validating SDTM, ADaM, and TLFs
- Good understanding of CDISC standards and clinical trial processes
Benefits
- 0% travel or less (remote)
- Best of both worlds: security + additional career opportunities
ClinChoice is a partner to pharmaceutical, medical device, and consumer care innovators, providing expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to support healthcare advancement and regulatory compliance.