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HomeCompaniesDa1455fc Edc0 4a7e A06e 849898ac32a2 19000101 000001Biostatistician - Contract

Biostatistician - Contract

Da1455fc Edc0 4a7e A06e 849898ac32a2 19000101 000001 · Remote, Virginia Beach, US, Virginia Beach · Remote · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
CompanyDa1455fc Edc0 4a7e A06e 849898ac32a2 19000101 000001
TitleBiostatistician - Contract
Normalized title-
Department / team-
LocationVirginia Beach, United States
Work modelRemote / Remote
Employment typeContract
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2023-07-06 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Da1455fc Edc0 4a7e A06e 849898ac32a2 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Virginia Beach.Open
Work model jobsActive Remote postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyDa1455fc Edc0 4a7e A06e 849898ac32a2 19000101 000001
Sourcef9b6e191-db37-461f-858b-5d073c49dfb3
ATS providerADP Workforce Now Recruiting

Description

Biostatistician – (Contract) The Biostatistician will perform statistical duties for one or more particular life science client projects, including clinical trial studies within the in-vitro diagnostic (IVD), medical device and pharmaceutical industry. Beaufort is a global CRO built around one purpose- helping life science companies improve and save lives through rapid development and commercialization of innovative products. Key responsibilities include: Conduct project planning activities such as: o Protocol and Case Report Form (CRF) Review o Sample size calculations o Statistical Analysis Plan (SAP) o Programming Plan (including analysis dataset specifications) Review project datasets and perform statistical analysis according to the plan (SAP). Incorporate client changes or modifications as required and provide documentation logs to include in the project/study files. Finalizes statistical analysis and final report for inclusion in the Clinical Study Report (CSR) and all appropriate project documentation. This includes tables, listings, and figures. Archive all documentation. Perform other project-related tasks assigned to the Statistician role as specified in the individual’s Statement of Work. Qualifications: Minimum of Master’s degree in statistics or biostatistics 5+ years of experience Top 3 skills needed to perform the work requested: Statistics, SAS programming skills, Knowledge of industry standards, Understanding of clinical trial data, preferably clinical trial data for in-vitro diagnostic trials Non-technical/ personal skills needed: Effective communication both verbally and written, team player Beaufort offers a different CRO experience. It’s not just about what we do, it’s how we do it. Together our team brings a level of passion, knowledge and commitment to our projects and clients. We foster a culture of excellence specializing in in-vitro diagnostics, clinical project management, quality oversight and regulatory solutions. At Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization. Beaufort is an equal opportunity employer and values diversity.

Full job record

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Provider Job Key448701
TitleBiostatistician - Contract
Normalized Title
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Activeyes
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Department
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CountryUnited States
Region
CityVirginia Beach
Salary Raw
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First Seen At2026-05-31 19:03:16Z
Last Seen At2026-06-06 13:32:23Z
Last Checked At2026-06-06 13:32:23Z
Last Changed At2026-06-06 13:32:23Z
Inactive At
Source Posted At2023-07-06 19:07:00Z
Source Updated At
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    "requisitionDescription": "<div><div>\n    <link href=\"https://static.workforcenow.adp.com/mas/mdf-components/23.18.17/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\" />\n    <link href=\"https://static.workforcenow.adp.com/mas/mdf-components/23.18.17/styles/froala_style.min.css\" rel=\"stylesheet\" type=\"text/css\" />\n\n    <div class=\"fr-view\">\n      <div><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/23.18.17/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\">&nbsp;<link href=\"https://static.workforcenow.adp.com/mas/mdf-components/23.18.17/styles/froala_style.min.css\" rel=\"stylesheet\" type=\"text/css\"><div class=\"fr-view\"><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;' id=\"isPasted\"><strong><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Biostatistician &ndash; (Contract)</span></strong></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><strong><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;</span></strong></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>The Biostatistician will perform statistical duties for one or more particular life science client projects, including clinical trial studies within the in-vitro diagnostic (IVD), medical device and pharmaceutical industry. &nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;line-height:107%;font-family:\"Verdana\",sans-serif;'>Beaufort is a global CRO built around one purpose- helping life science companies improve and save lives through rapid development and commercialization of innovative products.&nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><br></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><strong><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Key responsibilities include:</span></strong></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;margin-left:1.0in;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp;</span></p><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left:-0.25in;\"><li style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-family:\"Verdana\",sans-serif;font-size:13px;'>Conduct project planning activities such as:</span></li></ul></div><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.75in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;text-indent:-.25in;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>o</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp; &nbsp;</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Protocol and Case Report Form (CRF) Review</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.75in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;text-indent:-.25in;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>o</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp; &nbsp;</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Sample size calculations</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.75in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;text-indent:-.25in;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>o</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp; &nbsp;</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Statistical Analysis Plan (SAP)</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.75in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;text-indent:-.25in;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>o</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp; &nbsp;</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Programming Plan (including analysis dataset specifications)</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.25in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp;</span></p><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left:-0.25in;\"><li style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-family:\"Verdana\",sans-serif;font-size:13px;'>Review project datasets and perform statistical analysis according to the plan (SAP).&nbsp;</span></li></ul></div><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left:-0.25in;\"><li style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-family:\"Verdana\",sans-serif;font-size:13px;'>Incorporate client changes or modifications as required and provide documentation logs to include in the project/study files.&nbsp;</span><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp;</span></li></ul></div><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left:-0.25in;\"><li style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-family:\"Verdana\",sans-serif;font-size:13px;'>Finalizes statistical analysis and final report for inclusion in the Clinical Study Report (CSR) and all appropriate project documentation. This includes tables, listings, and figures. Archive all documentation. &nbsp;</span></li></ul></div><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left:-0.25in;\"><li style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-family:\"Verdana\",sans-serif;font-size:13px;'>Perform other project-related tasks assigned to the Statistician role as specified in the individual&rsquo;s Statement of Work.</span></li></ul></div><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.25in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;text-indent:-.25in;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><strong><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Qualifications:</span></strong></p><ul style=\"list-style-type: disc;margin-left:-0.25in;\"><li><span style='font-family:\"Verdana\",sans-serif;font-size:13px;'>Minimum of Master&rsquo;s degree in statistics or biostatistics</span></li><li><span style='font-family:\"Verdana\",sans-serif;font-size:13px;'>5+ years of experience&nbsp;</span></li></ul><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;margin-left:.25in;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><strong><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>Top 3 skills needed to perform the work requested:</span></strong></p><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left:-0.25in;\"><li style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='line-height:115%;font-family:\"Verdana\",sans-serif;font-size:13px;'>Statistics, SAS programming skills, Knowledge of industry standards, Understanding of clinical trial data, preferably clinical trial data for in-vitro diagnostic trials</span></li></ul></div><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:-.25in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;'><strong><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp; &nbsp;</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:-.25in;line-height:normal;font-size:15px;font-family:\"Calibri\",sans-serif;'><strong><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp; &nbsp; &nbsp;Non-technical/ personal skills needed:</span></strong></p><div style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><ul style=\"margin-bottom:0in;list-style-type: disc;margin-left:-0.25in;\"><li style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='line-height:115%;font-family:\"Verdana\",sans-serif;font-size:13px;'>Effective communication both verbally and written, team player</span></li></ul></div><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><br></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;line-height:107%;font-family:\"Verdana\",sans-serif;'>Beaufort offers a different CRO experience. It&rsquo;s not just about what we do, it&rsquo;s how we do it. &nbsp; Together our team brings a level of passion, knowledge and commitment to our projects and clients. &nbsp;We foster a culture of excellence specializing in in-vitro diagnostics, clinical project management, quality oversight and regulatory solutions. &nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;line-height:107%;font-family:\"Verdana\",sans-serif;'>At Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization.</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:107%;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;line-height:107%;font-family:\"Verdana\",sans-serif;'>Beaufort is an equal opportunity employer and values diversity. &nbsp;</span></p><p style='margin:0in;font-size:15px;font-family:\"Calibri\",sans-serif;'><span style='font-size:13px;font-family:\"Verdana\",sans-serif;'>&nbsp;</span></p></div></div>\n    </div>\n  </div></div>\n",
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    "requisitionTitle": "Biostatistician - Contract",
    "clientRequisitionID": "1023",
    "organizationalUnits": [],
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}
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GET https://api.bluedoor.sh/job-postings/v1/jobs/192fd05aec5f070fd5f8143166125cdcd5f1a674?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/2f021871-cb14-4ef2-bb41-d58af356c198JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/f9b6e191-db37-461f-858b-5d073c49dfb3JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/192fd05aec5f070fd5f8143166125cdcd5f1a674/eventsJSON