biostatistician

Smart Research System

<p><b>BIOSTATISTICIAN</b></p><p><b>Section:</b> Clinical Trials Unit<br/><b>Division:</b> Research<br/><b>Location:</b> Abu Dhabi</p><p><b>Role Overview</b></p><p>We are hiring a <b>Biostatistician</b> to support clinical trials and research studies within a <b>hospital‑based Clinical Trials Unit</b>. The role focuses on statistical planning, analysis, and interpretation of clinical research data in compliance with regulatory standards.</p><p><b>Key Requirements</b></p><ul><li><b>Minimum 8-10 years of biostatistics experience</b></li><li><b>Hospital or healthcare research experience is mandatory</b></li><li>Experience supporting <b>clinical trials, medical research, or healthcare studies</b></li><li>Strong knowledge of statistical methods used in clinical research</li><li>Ability to interpret and present statistical results to non‑statistical stakeholders</li></ul><p><b>Key Responsibilities</b></p><ul><li>Provide statistical support for <b>clinical trials and research studies</b></li><li>Contribute to study design, sample size calculations, and statistical analysis plans</li><li>Perform statistical analysis and data interpretation</li><li>Support preparation of study reports, manuscripts, and regulatory submissions</li><li>Ensure compliance with <b>ICH‑GCP and research governance standards</b></li><li>Collaborate with investigators, coordinators, and data teams</li><li>Maintain documentation for statistical methods and analyses</li><li>Support audits and regulatory reviews as required</li></ul><p><b>Preferred Experience</b></p><ul><li>Experience working within a <b>Clinical Trials Unit or hospital research environment</b></li><li>Proficiency in <b>SAS, R, SPSS, or STATA</b></li><li>Experience supporting publications and research presentations</li></ul><p>✅ <b>Important Note</b></p><p>This role is <b>strictly for candidates with prior hospital or healthcare experience</b>.<br/>Applications without relevant healthcare exposure <b>will not be considered</b>.</p><p>Job Types: Full-time, Permanent</p><p>Pay: AED28,000.00 - AED38,000.00 per month</p><p>Work Location: In person</p>

Biostatistician

Qatar University

<div><ul><li>Design and implement biostatistical and bioinformatics pipelines for omics and large-scale biological data (e.g., genomics, transcriptomics, epigenetics, metabolomics)</li><li>
Perform complex statistical analyses, including modeling, hypothesis testing, and predictive analytics</li><li>
Provide consultation on experimental design and assist in interpreting results with a strong emphasis on scientific rigor</li><li>
Support and co-author scientific publications, grants, and research proposals in coordination with faculty and research teams</li><li>
Collaborate across interdisciplinary teams including clinicians, laboratory scientists, computational biologists, and project managers</li><li>
Lead the integration of data pipelines and platforms, ensuring compatibility with clinical and research standards</li><li>
Mentor junior staff, including training in biostatistics and bioinformatics tools and best practices</li><li>
Participate in recruitment efforts and contribute to the development of a bioinformatics/biostatistics section</li><li>
Remain current with methodological advancements in bioinformatics, statistics, and data science</li></ul>
Qualifications
<p> PhD in Biostatistics or related field</p>
Required Documents
<div><b>Non Academic:</b></div>
<div><ul><li>Curriculum Vitae with cover letter.</li></ul>
<ul><li>Experience Certificates.</li></ul>
<ul><li>At least three references including contact numbers and email addresses.</li></ul>
<ul><li>Highest Academic Qualification.</li></ul></div>
<b>Academic:</b>
<div><ul><li>Current Curriculum Vitae with Cover letter.</li></ul>
<ul><li>Teaching,research, and service philosophy.</li></ul>
<ul><li>Three referees&rsquo; contact information (physical and email addresses as well their telephones contact).</li></ul>
<ul><li>Copy of highest earned credential (transcript of highest degree if graduated from an institution where course work was completed.However, if no course work was completed,an copy of certificate letter from the registrar of your highest credential granting institution regarding your highest academic degree).</li></ul>
<ul><li>Any additional documentation that you feel is relevant to your application.</li></ul></div>
Benefits
<div><b>Non Academic:</b></div>
<div><ul><li>Competitive tax-free salary.</li></ul>
<ul><li>Housing allowance in accordance with HRM Law.</li></ul>
<ul><li>Annual air tickets for candidate and dependents according to QUHR policies.</li></ul>
<ul><li>Public health care and health insurance to candidate and family members according to QU HR policies.</li></ul>
<ul><li>Annual leave in accordance with HRM Law.</li></ul>
<ul><li>End-of-contract indemnity.</li></ul></div>
<b>Academic:</b>
<div><ul><li>A three-year renewable contract.</li></ul>
<ul><li>Salary is commensurate with experience.</li></ul>
<ul><li>Tax-free salary.</li></ul>
<ul><li>Furnished accommodation in accordance with QU HR policies.</li></ul>
<ul><li>Annual air tickets for faculty member and dependents in accordance with QU HR policies.</li></ul>
<ul><li>Educational allowance for candidate's children (eligible candidates only) in accordance with QU HR policies.</li></ul>
<ul><li>Private health care and health insurance in accordance with QU HR policies.</li></ul>
<ul><li>Annual leave in accordance with QU HR policies.</li></ul>
<ul><li>End-of-contract indemnity.</li></ul></div>
How To Apply <b>New Applicant:</b> You need to setup an account with QU Recruitment Online website (https://careers.qu.edu.qa) and complete your personal profile. Once your profile is complete you may use it to apply for an open Position.</div>

サイネオス・ヘルス

<div><div><div><p><b>Updated:</b> Yesterday<br>
<b>Location:</b> Nida Kule Iş Merkezi G&ouml;ztepe, 34, Turkey<br>
<b>Job ID:</b> 25106917-OTHLOC-4595-2DR
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</div></div><div><p><b>Description</b>
</p>Principal Biostatistician - Biomarker (EMEA Remote)<p></p><div>
Syneos Health&reg; is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.<br>
<br>
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
<br>
<br>
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver &ndash; for one another, our customers, and, most importantly, for those in need.
<br>
<br>
Discover what your 25,000 future colleagues already know:
<br>
<br>
Why Syneos Health<br>
<ul><li>We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.</li><li>We are committed to building an inclusive culture &ndash; where you can authentically be yourself. Central to this is our purpose &ndash; Driven to Deliver &ndash; which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone&rsquo;s life.
</li><li>We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.</li></ul></div><p></p><p><b>
Job Responsibilities</b></p><p></p><div><div><p><b>
Major tasks:</b></p></div><div><ul><li><p>
Collaborates with representatives from other functions to plan, execute and analyze all biomarker aspects (including genomics) of clinical studies or biomarker studies in the role of the biomarker statistician and assumes the role of project biomarker statistician under guidance of an experienced statistician</p></li></ul></div><div><ul><li><p>
Develops the Biomarker Evaluation Plan for the study as appropriate, ensuring overall consistency within and between projects</p></li></ul></div><div><ul><li><p>
Provides statistical input in clinical development discussions, and usage of AI and ML approaches.</p></li></ul></div><div><ul><li><p>
Facilitates the overall organization and coordination of statistical activities regarding biomarker research and development activities for specific studies and projects</p></li></ul></div><div><ul><li><p>
Conduct and design advanced data analysis for genomics and biomarker statistics, including statistical programming, and design complex analysis algorithms.</p></li></ul></div><div><ul><li><p>
Experience with RNA, olink and other biomarker data handling experience</p></li></ul></div><div><ul><li><p>
Assumes responsibility for the production and accuracy of the Biomarker Evaluation Report with respect to statistical deliverables and interpretation of the results.</p></li></ul></div><div><ul><li><p>
Works independently at routine and complex statistical questions, modeling and tasks.</p></li></ul></div><div><ul><li><p>
Develops and implements standard processes for the analysis of routine (parts of) biomarker assessments.</p></li></ul></div><p></p><div><p><b><br>
Qualifications</b></p></div><div><ul><li>PhD or MSc in Biostatistics, Statistics or Mathematics, or related field</li></ul></div></div><div><ul><li>Strong communication and interpersonal skills</li></ul></div><div><ul><li>Ability to work independently as well as collaboratively, as required.</li></ul></div><div><ul><li>Minimal supervision required.</li></ul></div><div><ul><li>Usage of AI and ML approaches</li></ul></div><div><ul><li>Previous experience in independently leading biomarker study mandatory</li></ul></div><div><p>
 &middot; Previous clinical trial experience, industry experience is preferred</p></div><div><ul><li>Strong knowledge on Biomarker evaluation, esp. In immunology and infections, type I diabetes, relevant parameters and underlying biology</li></ul></div><div><ul><li>Good knowledge of statistical programming languages including R (Bioconductor package and other relevant R packages for genetic data), Python</li></ul></div><div><ul><li>Analysis of high-dimensional data</li></ul></div><p></p><p><b>
Get to know Syneos Health</b></p><p><br>
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.</p><p></p><p>
No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.</p><p></p><p>
http://www.syneoshealth.com</p><p></p><p><b>
Additional Information</b></p><p><br>
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.</p><p><b>
Summary</b>
</p><ul><li>Hiring in select Europe countries only. Candidates must require no VISA sponsorship. This position is responsible for leading projects across multiple studies or programs. A Senior Biostatistician acts as the primary contact with the sponsor for all biostatistics related activities on assigned projects. This project will focus on Biomarker data.</li></ul></div></div></div></div><div></div>

Principal Biostatistician - Biomarker (EMEA Remote)

Syneos Health

<div>
 <strong>
  Description
  <br/>
  <br/>
 </strong>
 Principal Biostatistician - Biomarker (EMEA Remote)
 <br/>
 <br/>
 Syneos Health&reg; is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.
 <br/>
 <br/>
 Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
 <br/>
 <br/>
 Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you&rsquo;ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver &ndash; for one another, our customers, and, most importantly, for those in need.
 <br/>
 <br/>
 Discover what your 25,000 future colleagues already know:
 <br/>
 <br/>
 Why Syneos Health
 <br/>
 <br/>
 <ul>
  <li>
   We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  </li>
  <li>
   We are committed to building an inclusive culture &ndash; where you can authentically be yourself. Central to this is our purpose &ndash; Driven to Deliver &ndash; which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone&rsquo;s life.
  </li>
  <li>
   We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Job Responsibilities
  <br/>
  <br/>
 </strong>
 <strong>
  Major tasks:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Collaborates with representatives from other functions to plan, execute and analyze all biomarker aspects (including genomics) of clinical studies or biomarker studies in the role of the biomarker statistician and assumes the role of project biomarker statistician under guidance of an experienced statistician
  </li>
  <li>
   Develops the Biomarker Evaluation Plan for the study as appropriate, ensuring overall consistency within and between projects
  </li>
  <li>
   Provides statistical input in clinical development discussions, and usage of AI and ML approaches.
  </li>
  <li>
   Facilitates the overall organization and coordination of statistical activities regarding biomarker research and development activities for specific studies and projects
  </li>
  <li>
   Conduct and design advanced data analysis for genomics and biomarker statistics, including statistical programming, and design complex analysis algorithms.
  </li>
  <li>
   Experience with RNA, olink and other biomarker data handling experience
  </li>
  <li>
   Assumes responsibility for the production and accuracy of the Biomarker Evaluation Report with respect to statistical deliverables and interpretation of the results.
  </li>
  <li>
   Works independently at routine and complex statistical questions, modeling and tasks.
  </li>
  <li>
   Develops and implements standard processes for the analysis of routine (parts of) biomarker assessments.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   PhD or MSc in Biostatistics, Statistics or Mathematics, or related field
   <br/>
  </li>
 </ul>
 <ul>
  <li>
   Strong communication and interpersonal skills
   <br/>
  </li>
 </ul>
 <ul>
  <li>
   Ability to work independently as well as collaboratively, as required.
  </li>
  <li>
   Minimal supervision required.
  </li>
  <li>
   Usage of AI and ML approaches
  </li>
  <li>
   Previous experience in independently leading biomarker study mandatory
   <br/>
  </li>
 </ul>
 <ul>
  <li>
   Previous clinical trial experience, industry experience is preferred
  </li>
  <li>
   Strong knowledge on Biomarker evaluation, esp. In immunology and infections, type I diabetes, relevant parameters and underlying biology
   <br/>
  </li>
 </ul>
 <ul>
  <li>
   Good knowledge of statistical programming languages including R (Bioconductor package and other relevant R packages for genetic data), Python
   <br/>
  </li>
 </ul>
 <ul>
  <li>
   Analysis of high-dimensional data
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Get to know Syneos Health
  <br/>
  <br/>
 </strong>
 Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
 <br/>
 <br/>
 No matter what your role is, you&rsquo;ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
 <br/>
 <br/>
 http://www.syneoshealth.com
 <br/>
 <br/>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
 <br/>
 <br/>
 <strong>
  Summary
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Hiring in select Europe countries only. Candidates must require no VISA sponsorship. This position is responsible for leading projects across multiple studies or programs. A Senior Biostatistician acts as the primary contact with the sponsor for all biostatistics related activities on assigned projects. This project will focus on Biomarker data.
  </li>
 </ul>
</div>


AbbVie

<div><b>Company Description</b><p><b><br>
About AbbVie</b></p><p>
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.</p><b><br>
Job Description</b><p><br>
The role of the Senior Statistical Analyst is to perform statistical programming activities for all assigned Phase I-IV clinical studies sponsored by AbbVie and its partners. This position performs statistical programming for clinical studies, integrated summaries, and in support of responses to requests from regulatory authorities. This position can serve as a study lead for an assigned study.</p><p><b>
Responsibilities:</b></p><ul><li>
Leads the statistical programming activities, and provide programming and documentation support for multiple studies with high quality</li><li>
Review statistical analysis plans for all assigned studies and integrated summaries in conjunction with program lead and provide comments to study biostatistician</li><li>
Create ADaM data set specifications and data set for all assigned studies and integrated summaries</li><li>
Ensure study analysis is consistent with standard templates and specifications</li><li>
Contribute to submission support and support urgent regulatory agency requests</li><li>
Follow timelines for assigned study tasks</li><li>
Coordinate own task assignments</li><li>
Participating in a Statistical Programming process improvement initiative</li><li>
Manage timelines and ensure good communication with CROs/FSPs, internal programmers, statistics, data management, medical writing, regulatory publishing and clinical operations.</li><li>
Oversee programming tasks for a single study</li><li>
Conduct high level review of deliverables provided by CRO/FSP to ensure good quality and accuracy</li></ul><br>
<b>
Qualifications</b><p><br>
<b>Minimum Qualifications:</b></p><ul><li>
Degree in Statistics, Mathematics, or Engineering</li><li>
6+ years of relevant experience (with MS). OR 8+ years of relevant experience (with BS).</li><li>
Experience with SAS programming related to drug development</li><li>
Experience with regulatory filings</li><li>
Experience adhering to CDISC standards and creating and reviewing ADaM speicifications</li></ul><p><b>
Preferred Qualifications:</b></p><ul><li>
Knowledge of R or Ai is not required but can be a plus.</li></ul><p><b>
Other Required Skills:</b></p><ul><li>
In-depth understanding of SAS programming concepts and techniques related to drug development.</li><li>
Fundamental understanding of CDISC Standards.</li><li>
Fundamental understanding of the drug development process.</li><li>
Ability to communicate clearly both oral and written.</li><li>
Ability to accurately estimate effort required for study related programming activities.</li></ul><br>
<b>
Additional Information</b><p><br>
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
</p><ul><li><p>The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role atthe time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors includinggeographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
</p></li><li><p>We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
</p></li><li><p>This job is eligible to participate in our short-term incentive programs.
</p></li></ul><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested,and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to aparticular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company&rsquo;s sole and absolute discretion,consistent with applicable law.</p><div></div><p>
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.</p><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

Senior Statistical Analyst - Programmer (Hybrid)

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