London, England, United Kingdom Hybrid / WFH Options
Pear Bio
computational oncology, machine learning, and data science methodologies. Manage multiple projects simultaneously and ensure timely, high-quality deliverables. Must-Haves: MSc/PhD in data science, computational biology, bioinformatics, biostatistics, or a related field. 3+ years of professional experience in biotech, pharma, or academia focusing on life science projects (ideally oncology drug discovery). Strong foundation in statistics, data analysis More ❯
company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality biostatistics, programming, data management and data science services. With offices across the UK, US, Germany, Denmark, Kenya, Australia, India, China and Japan, Phastar is the second largest specialized biometrics provider globally More ❯
Cambridge, Cambridgeshire, United Kingdom Hybrid / WFH Options
Healthcare Businesswomens Association
let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range $93,800.00 - $174,200.00 Skills Desired Biostatistics, Computer Programming, Data Analysis, Databases, Data Management, Data Mining, Data Quality, Data Visualization, Deep Learning, Graph Algorithms, High-Performance Computing, Logistic Regression Model, Machine Learning (Ml), Master Data Management, Pandas More ❯
inform internal teams and external stakeholders. Lead simultaneous client facing projects across ZS Discovery to reinvent pharmaceutical discovery, elucidate complex disease biology and pioneer novel therapeutics. Provide expertise in biostatistics and/or bioinformatics applications, such as epidemiology, population genetics, genomics, proteomics, bulk or single cell RNA-sequencing, and/or systems biology. Partner with ZS leaders and client service More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
define.xml files, develop and maintain macros, and perform data integrity checks, while ensuring proper documentation and compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data More ❯
