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 CVRM team.
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.
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Skills Required
- Strong SAS programming experience within the pharmaceutical/CRO industry.
- Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies.
- Experience 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.
- Strong communication and stakeholder management skills.
- Bachelor's degree in computer science, statistics, or related scientific discipline with 5 years clinical programming (CDISC) experience; Master's with 6 years clinical programming (CDISC) experience.
- Respiratory/Immunology therapeutic area experience (in addition to CVRM experience noted).
- Working knowledge of ICH and Good Clinical Practices, clinical research, clinical trial process, and related regulatory requirements and terminology.
ClinChoice Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ClinChoice and has not been reviewed or approved by ClinChoice.
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Flexible Benefits — Flexible arrangements, including telecommuting and flextime with no core hours in some regions, are highlighted for many roles. Feedback suggests flexibility is commonly available but depends on role and location.
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Leave & Time Off Breadth — Vacation, personal, and sick days are part of the core package, with some markets granting paid leave from the date of hire. Feedback suggests time off is standard-to-decent across locations, though specifics vary.
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Healthcare Strength — Health coverage is positioned as a core benefit, with some accounts describing overall benefits as full or good. In the U.S., healthcare sits within a conventional CRO package alongside medical, dental, and vision.
ClinChoice Insights
What We Do
ClinChoice is a global full-service Contract Research Organization (CRO) specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies, aiming to accelerate the development and commercialization of innovative drugs and devices.
