18 of 18 Biostatistics Jobs in the East Midlands

companies Experience from successfully managing client’s Sr/VP level data science and procurement sponsors Masters or Doctorate degree in: Public Health, Epidemiology, Biostatistics, Healthcare Informatics, or a related discipline More ❯

companies Experience from successfully managing client’s Sr/VP level data science and procurement sponsors Masters or Doctorate degree in: Public Health, Epidemiology, Biostatistics, Healthcare Informatics, or a related discipline More ❯

companies Experience from successfully managing client’s Sr/VP level data science and procurement sponsors Masters or Doctorate degree in: Public Health, Epidemiology, Biostatistics, Healthcare Informatics, or a related discipline More ❯

companies Experience from successfully managing client’s Sr/VP level data science and procurement sponsors Masters or Doctorate degree in: Public Health, Epidemiology, Biostatistics, Healthcare Informatics, or a related discipline More ❯

companies Experience from successfully managing client’s Sr/VP level data science and procurement sponsors Masters or Doctorate degree in: Public Health, Epidemiology, Biostatistics, Healthcare Informatics, or a related discipline More ❯

companies Experience from successfully managing client’s Sr/VP level data science and procurement sponsors Masters or Doctorate degree in: Public Health, Epidemiology, Biostatistics, Healthcare Informatics, or a related discipline More ❯

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. More ❯

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. More ❯

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. More ❯

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. More ❯

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. More ❯

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. More ❯

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their More ❯

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their More ❯

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their More ❯

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their More ❯

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their More ❯

for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their More ❯