Clinical Statistician

ROLE SUMMARY - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

Job Summary:We are seeking a skilled Data Scientist to develop ADaM datasets, TLFs and analytical outputs for clinical trials.Responsibilities:Develop high-quality ADaM datasets and TLFs using R programming.Ensure accuracy, consistency and regulatory compliance in data deliverables.Contribute to Integrated Summary of Safety (ISS) and Integrated Summary of...

Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field. - At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. - Statistical Programming and SAS hand-on experience - Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial...

Use Your Power for PurposeAt Pfizer, our mission is to improve patients' lives through groundbreaking research and development. You will play a crucial role in this mission by ensuring our evidence is scientifically robust and providing essential expertise to guide healthcare decisions. Your work will directly impact the safety, efficacy, and marketability...

A productive, hands-on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role. - Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they...

Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field. - At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency. - Statistical Programming and SAS hand-on experience - Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial...

Job Summary:We are seeking an experienced SAS Programmer to join our team. The ideal candidate will have expertise in statistical programming, data analysis, and data management, particularly in the healthcare, pharmaceutical, or clinical research industries. The SAS Programmer will be responsible for designing, developing, and implementing SAS programs for...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

An Individual Contributor role Productive hands on programming supporting deliverables in the study project portfolio standards team of medium - high complex statistical programming deliverables to support assets and study teams Performs tasks independently with mentorship or advise from Programming Leads within the organization Acts as co-lead lead on...

At least 7-8 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.Accountable for multiple projects/ongoing work activities (timelines, work plans, deliverables) of moderate complexity within a Work TeamContributes to upto 70% of their time to programming deliverables assigned within the scope of the function in either SAS, R or...