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Need to have Oncology TA experience.

Need to have Oncology TA experience.

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. #LI-TT1 #LI-Remote #Senior #Contract

We’re seeking several Statistical Programmers II to join this growing organisation remotely from the UK. If this opportunity is of interest, please apply now with your CV, as the organisation is looking to arrange interviews for the Statistical Programmer II role as soon as possible. Statistical P

We have an exciting opportunity for a Principal or Senior level Statistical Programmer skilled in SAS to join us on a permanent basis in the UK. The Senior or Principal Programmer may also perform a supervisory role (e.

Senior Statistical Programmer/Analyst Consultant specializing in Respiratory & Immunology in the United Kingdom.

AIXIAL GROUP is seeking an experienced Senior Statistical Programmer to join our team. You'll be responsible for creation and quality control of statistical datasets and leading statistical programming activities for clinical trials. Candidates should possess a BSc/BA in relevant fields, excellent k

ClinChoice is seeking a Senior Statistical Programmer/Analyst Consultant to work in oncology.

Novartis Farmacéutica in Greater London seeks a Senior Principal Programmer to oversee statistical programming for various studies. Responsibilities include leading statistical programming activities, coordinating programming decisions, and ensuring quality outputs for regulatory submissions.

Our client is seeking an experienced Statistical Programmer as a full time contractor for 6‑months. The successful candidate will work closely with the Head of Statistics, an existing Statistical Programmer, and the wider research team to deliver on an exciting new project looking at the disease c

Cytel is seeking a Principal Statistical Programmer to support their pharmaceutical clients.

As Lead Statistical Programmer, primarily responsible for all statistical programming activities on assigned studies including planning and coordination of activities for assigned statistical programming team members. The ability to perform all duties of Lead Statistical Programmer on several concur

Senior Statistical Programmer Consultant. 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 inform

Lead statistical programming activities as Trial Programmer for either a large/pivotal study or several studies, or act as a Lead/Program Programmer for a small to medium sized project in phase I to IV clinical studies in Novartis Global Drug Development. The Principal Statistical Programmer is resp

A leading pharmaceutical consulting firm in the United Kingdom is seeking a Principal Statistical Programmer. You will be responsible for generating SDTM, ADaM specifications, and overseeing CRO statistical programming deliverables.

Novartis Farmacéutica is seeking a Principal Statistical Programmer in Greater London, responsible for overseeing statistical programming and analytics for clinical studies. The ideal candidate should possess a strong educational background in statistics or a related field, with extensive experienc

Senior Statistical Programmer/Analyst Consultant- (Respiratory & Immunology) (Outside IR35). Senior Statistical Programmer Consultant. Senior Statistical Programmer Consultant.

Pop Science is seeking an experienced Statistical Programmer for a 6-month full-time contract in Greater London.

Acts as the lead statistical programmer. Extensive programming experience in SAS or other required software, preferably in a clinical trial environment as demonstrated by the ability to lead multiple complex and/or global projects with teams of statistical programmers. R Statistical Programmer - Sub

We have an exciting opportunity for a Principal or Senior level Statistical Programmer skilled in SAS to join us on a permanent basis in the UK. The Senior or Principal Programmer may also perform a supervisory role (e.

Statistical Programmer II | Leading CRO | Home Based | UK |. We’re seeking several Statistical Programmers II to join this growing organisation remotely from the UK. If this opportunity is of interest, please apply now with your CV, as the organisation is looking to arrange interviews for the Stat

Senior Statistical Programmer I / II | Leading CRO | Home Based | UK | Permanent |. We’re seeking several Senior Statistical Programmers to join this growing organisation remotely from anywhere in the UK. If this opportunity is of interest, please apply now with your CV as the organisation are loo

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