senior biostatistician

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)

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

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>


Bristol Myers Squibb

<div><b>Working with Us</b><br>
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.<br>
<br>
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .<br>
<br>
This role leads biostatistics and serves as the DQS Lead, the quantitative authority on the global program team, translating complex data into clear, decision-shaping insights that inform program strategy, governance, and regulatory decisions.<br>
<br>
The Senior Director is responsible for providing statistical input to development strategies, and effective implementation plans to support product development or market access objectives in a global organization. provides expertise and guidance in collaboration with cross-functional groups broadly across the organization in establishing study design and analyses and strategy, and institutes best practices with regards to planning, execution, interpretation and regulatory submission of clinical projects and studies. Provides guidance and management to statisticians to ensure high quality and timely deliverables. Manages resources, sets priorities, and ensures consistency and adherence to standards therein. Through matrix leadership across DQS functions, the DQS Lead ensures high-quality, fit-for-purpose execution, proactively manages risk, and partners with cross-functional leaders to drive impactful, defensible decisions that accelerate delivery of medicines to patients. The Senior Director leads and develops teams in a matrixed global environment, sets priorities and allocates resources to protect portfolio milestones, and partners cross-functionally to ensure compliant, scalable execution and an inclusive culture where talent can thrive<br>
<br>
<b>Accountabilities:</b><br>
<ul><li>Uses leading edge and broad knowledge to lead highly complex projects. Provides in-depth analyses and recommendations to senior management.</li><li>Develops strategy for area managed and directly contributes to strategy of function.</li><li>Decisions impact broader organization, region, or multiple sites.</li></ul><br>
<b>
People Management Accountabilities:</b><br>
<ul><li>Provides leadership and direction through multiple levels of managers and/or expert-level individual contributors across varied departments.</li><li>Directly accountable for the performance and results of a large department, region or key market, or complex/multiple sites.</li><li>Develops function's strategy and directly contributes to broader organization's strategy development.</li></ul><br>
<b>
Key Responsibilities:</b><br>
Develops and reviews statistical analysis plans and ensures they are aligned with study objectives and regulatory requirements.<br>
Provides expert statistical guidance into clinical development plans, clinical study protocols, clinical study reports, regulatory submission documents and publications to ensure accurate deliverables.<br>
Provides statistical leadership and support for feasibility assessments, clinical development plans, complex study designs, regulatory meetings, submissions and follow up.<br>
Manages relationships with external partners and vendors to ensure the quality and timeliness of statistical deliverables.<br>
Leads the development and adaptation of new statistical methodologies in support of drug research and development, keeping current with regulatory guidance and requirements.<br>
Leads and oversees the biostatistics team, ensuring delivery of statistical analysis plans and reports for clinical trials.<br>
<br>
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
<br>
<br>
<b>Compensation Overview:</b><br>
<br>
Princeton - NJ - US: $249,480 - $302,305
<br>
<br>
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
<br>
<br>
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
<br>
<br>
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
<ul><li><b>Health Coverage:</b> Medical, pharmacy, dental, and vision care.</li><li>
<b>Wellbeing Support:</b> Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
</li><li><b>Financial Well-being and Protection:</b> 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
</li></ul><b>Work-life benefits include:
</b><br>
<br>
Paid Time Off
<ul><li>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
</li><li>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
</li></ul>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
<br>
<br>
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.<br>
<br>
<ul><li><b>Eligibility Disclosure: </b>T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
</li></ul><br>
<b>Uniquely Interesting Work, Life-changing Careers</b><br>
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.<br>
<br>
<b>On-site Protocol</b><br>
<br>
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
<br>
<br>
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
<br>
<br>
<b>Supporting People with Disabilities</b><br>
<br>
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
<br>
<br>
<b>Candidate Rights</b><br>
<br>
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
<br>
<br>
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
<br>
<br>
<b>Data Protection</b><br>
<br>
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection .<br>
<br>
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.<br>
<br>
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
<br>
<br>
R1601017 : Senior Director, Biostatistics</div>

Senior Director, Biostatistics

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>

ICR, Inc.

<div><div><b>Bayesian Statistician (Data Scientist)</b><br>
Aurora, CO</div>
<div></div><div>Applications will be accepted on an ongoing basis.</div><br>
<div><br>
<br>
ICR has opportunities available for experienced and motivated Data Scientists with a Bayesian statistics background.<br>
<br>
<b>Essential Job Responsibilities</b><br>
<br>
This Data Scientist will be expected to:</div>
<ul><li>Work independently on complex technical tasks that require in-depth data analysis methodologies and data/information collection</li>
<li>Develop unique technical solutions for applications in the intelligence field</li>
<li>Participate as a member of a multidisciplinary team to analyze and satisfy customer requirements</li>
<li>Develop, implement, validate, document, and present findings of specialized analysis software tools and models as required</li>
<li>Effectively handle concurrent technical tasks with conflicting priorities</li>
<li>Approach difficult problems with enthusiasm and creativity</li>
<li>Have the ability to change focus when necessary</li>
<li>Travel (up to 10%)</li>
</ul>
<div><br>
<b>Required Skills and Qualifications</b></div>
<ul><li>Active Top Secret Security Clearance with SSBI and SCI eligibility.</li>
<li>Experience with Bayesian statistics and time series analysis</li>
<li>Masters Degree in statistics with a minimum of Two (2) years of professional experience or PhD in statistics or related field
</li><li>Experience with computational analysis tools and developing software with at least one of the following programing language: Python (preferred), R, C++, MATLAB
</li><li>Experience with developing and applying advanced statistical/machine learning models and algorithms for one or more of the following: classification, clustering, anomaly detection, density estimation, data mining, pattern recognition, knowledge discovery</li>
<li>Experience with extracting and processing structured/unstructured data from various sources (e.g. databases, text files, web) and preparing data for analysis
</li><li>Collaborate with others in a multidisciplinary team environment to accomplish research goals
</li><li>Ability to work effectively in small-team settings to solve complex problems
</li><li>Ability and desire to obtain substantial domain knowledge in fields of application and ability to communicate effectively with subject matter experts
</li><li>Proficient verbal and written communication skills to collaborate effectively in a team environment and present and explain technical information to customers</li>
</ul>
<div><br>
<b>Desired Qualifications</b></div>
<ul><li>Experience with the intelligence community
</li><li>Broad knowledge of statistical analysis, ML methods, and problem-solving skills
</li><li>Experience with: spatial statistics, multivariate statistics, Gaussian Process, Random Forest, Support Vector Machine, Natural Language Processing, Neural Networks
</li><li>Proficient with Python, Jupyter, Markdown
</li><li>Experience working with databases such as SQL and/or ELK stack
</li><li>Experience with creating data visualizations / dashboards</li>
</ul>
<div></div><div>Salary Range: $78,853 - $236,579</div>
<div></div><div>This position offers a comprehensive benefits package that includes company equity, retirement plan, company-paid health care benefits, flexible paid time off policy, and opportunity for a raise and bonus during the year.</div><br>
<div></div>
<div></div><div><div><div>ICR, Inc. considers several factors when extending job offers, including but not limited to candidates&rsquo; key skills, relevant work and/or military experience, education, training certifications and work location.
</div>
<div></div><div><div><i>ICR is proud to be an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status, or any other protected factor.</i></div></div></div></div></div><div></div>

Bayesian Statistician (Data Scientist) - Aurora, CO

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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