Miami, FL · Remote
$60 - $70/hr
Strong documentation, communication, and analytical skills Qualifications * 5+ years of Biostatistics experience in clinical trials (Sponsor, CRO, or Academic Research). * MSc or PhD in Biostatistics ...
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Miami, FL · Remote
$60 - $70/hr
Strong documentation, communication, and analytical skills Qualifications * 5+ years of Biostatistics experience in clinical trials (Sponsor, CRO, or Academic Research). * MSc or PhD in Biostatistics ...
MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... High level knowledge of drug development as it pertains to biostatistics. * Provides support to ...
Quick apply
MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... High level knowledge of drug development as it pertains to biostatistics. * Provides support to ...
Miami, FL · On-site
$110 - $160/hr
MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We address the emerging analytics needs of the Industry with our biostatistics services, bespoke ...
Miami, FL · On-site
$110 - $160/hr
MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We address the emerging analytics needs of the Industry with our biostatistics services, bespoke ...
Miami, FL · On-site
MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We address the emerging analytics needs of the Industry with our biostatistics services, bespoke ...
Quick apply
Miami, FL · On-site
MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on ... We address the emerging analytics needs of the Industry with our biostatistics services, bespoke ...
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$60 - $70/hr
Full-time
Posted 26 days ago
Location: Remote
Job Type: Contractor
Pay: $60–$65/hour
We are looking for an experienced Biostatistician to support clinical research projects by analyzing clinical trial data, validating statistical outputs, and ensuring compliance with regulatory standards.
Key ResponsibilitiesAnalyze and validate clinical trial data.
Review and interpret Statistical Analysis Plans (SAPs).
Produce and quality-check Tables, Figures & Listings (TFLs).
Review Clinical Study Reports (CSRs) and regulatory submission data.
Perform statistical analyses using SAS and/or R.
Collaborate with cross-functional teams and document findings accurately.
SAS and/or R
CDISC SDTM & ADaM
SAP interpretation
Survival analysis, mixed models, covariate adjustment
Multiplicity control & ICH E9(R1)
Clinical trial data analysis
TFL production & QC
Regulatory submissions & CSR review
Strong documentation, communication, and analytical skills
5+ years of Biostatistics experience in clinical trials (Sponsor, CRO, or Academic Research).
MSc or PhD in Biostatistics, Statistics, or a related field.
Experience with regulatory submissions and statistical quality control is preferred.
