biostatistician

The Emmes Company, LLC

<div>Overview:
<div><b>
Lead Biostatistician</b></div><div></div><div><b><br>
India Remote/Bengaluru(hybrid)</b></div><div></div><div><br>
Emmes Group: Building a better future for us all.</div><div></div><div><br>
Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.</div><div></div><div><br>
We believe the work we do will have a direct impact on patients&rsquo; lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We&rsquo;re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!</div><div></div><div><b><br>
Primary Purpose</b></div><div>
The Biostatistician collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, performs statistical analysis and inference and writes and presents reports summarizing findings including publications in peer-reviewed journals. The Biostatistician develops systems for monitoring the quality of clinical data. The Biostatistician ensures high-quality statistical support is provided for clinical trials, registries and basic research using advanced statistical skills and knowledge of clinical research. The Biostatistician maintains expertise in state-of-the-art data manipulation and statistical methodology.</div>
Responsibilities:
<ul><li>Collaborates with clinical investigators to determine study design.</li><li>
Writes sections of protocols that require statistical input.</li><li>
Reviews protocols and case report forms to ensure that protocol objectives are met, and standards are maintained.</li><li>
Generates treatment allocations in randomized clinical research studies and ensures proper implementation.</li><li>
Leads the project team&rsquo;s development of statistical analysis plans and programs to perform analyses and display study data.</li><li>
Performs statistical analyses, writes and validates application programs.</li><li>
Implements data and safety monitoring reports to ensure participants safety.</li><li>
Develops metrics and generates quality control reports to optimize the performance of clinical sites and the coordinating center.</li><li>
Generates study reports to be distributed to internal and external monitoring committees and regulatory bodies.</li><li>
Applies, guides and ensures others on team are implementing QC processes, ensuring deliverables are accurate, are of high quality and delivered on agreed timelines.</li><li>
Authors or contributes to manuscripts and/or scientific presentations.</li><li>
Participates in professional development activities both within and outside the</li><li>
Ensure timely and effective communication of project milestones and status to internal stakeholders.</li><li>
Assists the cross functional communication for smooth deliverables of study related documents.</li><li>
Works with multi-disciplinary teams</li></ul>
Qualifications:
<ul><li>Requires a master&rsquo;s or PhD degree in Statistics with minimum of 6 years of clinical research experience.</li><li>
Solid understanding of design of experiments; Demonstrated proficiency with statistical methods and applications in clinical research.</li><li>
Competent in SAS programming language and/or R.</li><li>
Expertise in state-of-the-art data manipulation and statistical methodology.</li><li>
Ability to effectively communicate technical concepts, both written and oral.</li><li>
Ability to lead / drive departmental initiatives (with Supervision).</li><li>
Ability to supports recruitment activities in terms of interviewing candidates</li><li>
Flexibility in time management</li><li>
Good organizational and communication (written and oral) skills, ability to manage multiple tasks, ability to work with minimum supervision, as well as in a team environment and a desire to improve skills</li><li>
Professional speaking abilities for routine internal and/or external communication purposes.</li><li>
Be willing to learn and adapt to new processes and procedures.</li></ul><div><b>
CONNECT WITH US!</b></div><div><i>
Follow us on Twitter - @EmmesCRO</i></div><div><i>
Find us on LinkedIn - Emmes</i></div><div></div><div><br>
#LI-Remote</div></div>

Lead - Biostatistician

University Of Washington

<div><p><b>Job Description
</b></p><p></p><div><p>As a UW employee, you have a unique opportunity to change lives on our campuses, in our state and around the world. UW employees offer their boundless energy, creative problem-solving skills, and dedication to build stronger minds and a healthier world.<br>
</p></div><p></p><div><p>UW faculty and staff also enjoy outstanding benefits, professional growth opportunities and unique resources in an environment noted for diversity, intellectual excitement, artistic pursuits, and natural beauty.
</p></div><p></p><p><b>The Department of Medicine is seeking a highly skilled and experienced Biostatistician to join our team and serve as the Director of a new departmental Analytical Core.
</b><br>
<br>
The Department of Medicine is the largest department in the School of Medicine with over 3900 staff, faculty, trainees and students within eleven subspecialties divisions. Learn more about our department at https://medicine.uw.edu/index.php/about .
<br>
<br>
<b>ABOUT THE ROLE
</b><br>
The role of the Biostatistician and Director is to provide complex and critical consulting, leadership, statistical expertise, data analysis, and data interpretation services to advance and support the research community within the department and the university. The Biostatistician will have the opportunity to design and shape key processes and procedures in the Data Analytics Core. This position requires the ability to work independently, manage multiple overlapping data analysis projects, and communicate effectively with staff and faculty on a wide range of topics. Given the substantial volumes and diverse data types involved in these projects, fluency with various statistical/programming software is essential.
<br>
<br>
There is a growing need for multifaceted centralized analytic support within the Department of Medicine and the UW and the Biostatistician contributes to the growth and success by executing the department&rsquo;s mission and vision. The goal of this position is to provide and create department-wide biostatistical support for faculty-initiated projects as part of the departmental Data Analytics Core team. This position requires accuracy, efficiency, flexibility, creativity, and a desire to serve multiple stakeholders, while working within UW regulations. We anticipate near term growth; thus, the incumbent would also be responsible for recruiting and onboarding additional master&rsquo;s level analysts and leading the project management across the team.
<br>
<br>
The position reports to the Vice Chair of Research, and partners with multiple senior leaders in the department.
</p><p></p><p><b>DUTIES AND RESPONSIBILITIES
</b><br>
<b><i>Analytical = 75%
</i></b></p><ul><li><p>Research and determine appropriate methodologic procedures for a range of statistical analyses, including biostatistics and bioinformatics.
</p></li><li><p>Be able to perform multivariable statistical analyses using advanced analytic approaches.
</p></li><li><p>Collaborate with individuals or interdisciplinary research teams on projects from inception through publication. Tasks may include assessing feasibility, developing objective(s), performing sample size and power calculations, generating and implementing randomization schema, and writing statistical sections of research protocols and manuscripts (e.g., statistical analysis plan).
</p></li><li><p>Develop knowledge and skills in established and emerging analytical techniques.
</p></li></ul><p></p><p><b><i>Data Analytic Core Management = 25%
</i></b></p><ul><li><p>Direct day-to-day operations of the Data Analytic Core, including triaging requests for data analysis and overall project management
</p></li><li><p>Recruiting, onboarding, assigning projects, offboarding a team of data analysts.
</p></li><li><p>Advertise and promote the Core to the faculty and trainees, and provide consultation for new data analytic requests
</p></li><li><p>Work collaboratively across the Department and the School of Medicine to bring together a data analytic network
</p></li><li><p>Partner with the Senior Director of Operations and the CFO to ensure projects are being charged out appropriately and that there is a financial sustainability plan.
</p></li></ul><p></p><p><b>MINIMUM REQUIREMENTS
</b></p><ul><li>Doctoral Degree in Statistics, Biostatistics, Epidemiology or a related field and at least 2 years&rsquo; related experience with progressive responsibility at a diverse, complex, multi-faceted organization.
</li></ul><p><i>Equivalent education/experience will substitute for all minimum qualifications except when there are legal requirements, such as a license/certification/registration.
</i></p><p></p><p><b>A </b><b>D </b><b>DITIONAL REQUIREMENTS
</b></p><ul><li><p>Demonstrated dedication to equity, diversity and inclusion.
</p></li><li><p>Demonstrated experience and advanced knowledge with SAS, R, Python, STATA, or other coding language and programming software.
</p></li><li><p>Experience with federal grant submissions, including proposals to the NIH and DOD
</p></li><li><p>Strong analytical communication, critical thinking and problem-solving skills.
</p></li><li><p>Excellent time management skills and ability to prioritize projects.
</p></li><li><p>Strong focus and quality and timely delivery of work.
</p></li></ul><p></p><p><b>DESIRED QUALIFICATIONS
</b></p><ul><li><p>7 years' related experience
</p></li><li><p>Previous experience in a consultant-based model/shared service, research setting and/or medical setting.<br>
<br>
</p></li></ul><p><b>WORKING ENVIRONMENTAL CONDITIONS
</b><br>
&bull; In a deadline-driven environment, occasional evening or weekend hours may be required.
<br>
<br>
#UWDeptMedicineJobs
</p><p></p><p><b>Compensation, Benefits and Position Details
</b></p><p></p><p><b>Pay Range Minimum:
</b></p>$150,000.00 annual
<p><b>Pay Range Maximum:
</b></p>$185,904.00 annual
<p><b>Other Compensation:
</b></p><ul><li></li></ul><p><b>Benefits:
</b></p>For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/
<p><b>Shift:
</b></p>First Shift (United States of America)
<p><b>Temporary or Regular?
</b></p>This is a regular position
<p><b>FTE (Full-Time Equivalent):
</b></p>100.00%
<p><b>Union/Bargaining Unit:
</b></p>UAW Research
<p></p><p><b>About the UW
</b></p><p></p><p>Working at the University of Washington provides a unique opportunity to change lives &ndash; on our campuses, in our state and around the world.
</p><p></p><p>UW employees bring their boundless energy, creative problem-solving skills and dedication to building stronger minds and a healthier world. In return, they enjoy outstanding benefits, opportunities for professional growth and the chance to work in an environment known for its diversity, intellectual excitement, artistic pursuits and natural beauty.
</p><p></p><p><b>Our Commitment
</b></p><p></p><p>The University of Washington is proud to be an affirmative action and equal opportunity employer . All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, age, protected veteran or disabled status, or genetic information.
</p><p></p><p>To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 or dso@uw.edu .
</p><p></p><p>Applicants considered for this position will be required to disclose if they are the subject of any substantiated findings or current investigations related to sexual misconduct at their current employment and past employment. Disclosure is required under Washington state law .</p></div>

Biostatistician & Director

Unilever

<div><p><b>ABOUT UNILEVER
</b></p><p>With 3.4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people &ndash; we believe that when our people work with purpose, we will create a better business and a better world.</p><p></p><p><b>
Job Brief:</b></p><div>
The Clinical Biostatistics group is responsible for delivering leadership and expertise in the use of Statistics and Data Analytics across the Beauty &amp; Wellbeing and Personal Care (BW &amp; PC) Clinical Program. For Statistics this covers support in statistical design of clinical studies, statistical analysis, visualization of data and interpretation and reporting of results. Additionally, the group provides expertise in clinical data mining and modelling, and biostatistics support to the BWPC R&amp;D cross functional teams with respect to the clinical program and related areas. The group delivers via a highly skilled team that is aligned to specific program areas within BPC and works in close partnership with Clinical researchers as well as BWPC Science &amp; Technology (S&amp;T), Global Design, Category Design, and Cluster Design teams on a global level.<br>
<br>
<b>Requirements &amp; Qualifications:</b> The candidate should ideally have at least a master&rsquo;s degree in Statistics/Biostatistics, with three to six years&rsquo; experience in research or the FMCG/Pharmaceutical industries, although applications from less experienced candidates will be considered. Proficiency in SAS and R is essential, including the ability to automate routine tasks, develop macros, and build applications. Strong written and verbal communication skills are also required.<br>
<br>
<b>Responsibilities:</b><br>
<ul><li>Engagement and collaboration with globally deployed, multi-disciplinary teams to design and implement efficient, well-focused, statistically fit-for-purpose studies, analyse, visualise and interpret data.</li><li>Work in inter-disciplinary teams that includes clinical study experts, measurement scientists, bioinformaticians, and other statisticians, both within Unilever and with external partners.</li><li>Provision of statistical expertise across a range of R&amp;D disciplines to define and implement statistical solutions.</li><li>Deliver high quality statistical programming deliverables for all assignments that consistently meets study timelines, quality standards.</li><li>Responsibility for the quality and defensibility of study designs, statistical analyses, models and data interpretation.</li><li>Perform exploratory data analyses of clinical studies and reporting as required.</li><li>Follow all standard practices as per SOP&rsquo;s and guidance documents.</li></ul><br>
<b>
Key Accountabilities:</b><br>
<ul><li>Works as a member of a team to design and/or review protocols, case report forms, and other key study documents</li><li>Write and review statistical sections and other relevant parts of study synopses and protocols</li><li>Performs relevant sample size calculations</li><li>Design randomization plans and generates random allocation lists</li><li>Develops statistical analysis plans including analysis files and data reporting specifications</li><li>Develops appropriate statistical methods for data analysis and ensures the accuracy and reproducibility of data sets and analyses of clinical study data</li><li>Follows relevant work practices and procedures and organizational SoPs</li><li>Working closely with mutli-disciplinary teams to ensure a complete review of the data, providing a thorough understanding of statistical processes and issues that may arise in analysis</li><li>Plan the statistical analyses, programming and execution of the analyses, instructing and reviewing statistical planning and analysis work</li><li>Perform hands-on data analysis and modeling of obtained data to provide outputs that will guide in decision making through various stages of project</li><li>Liaises with other statisticians and scientists in areas of expertise and experience and ensures continuous improvement for themselves and the broader team via sharing of approaches and best practices;</li><li>Provides statistical consultancy as required to the R&amp;D programme.</li><li>Engages and collaborates with globally deployed, multi-disciplinary teams to design and implement efficient, well-focused, statistically fit-for-purpose studies. Teams may include clinicians, measurement scientists, bio scientists, product formulators, claims experts, and others;</li><li>Acts as secondary contact (supporting the Lead Statistician for the area) across multiple primary research areas (e.g. Skin Face Care, Microbiome, Skin cleansing, Hair Care, Oral, etc.);</li></ul></div><p></p><p><b>
Our commitment to Equality, Diversity &amp; Inclusion</b></p><p>
Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.</p><p></p><p><i>
&quot;All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent&mdash;please verify before proceeding.&quot;</i></p></div>

R&D Executive - Statistician

Amgen

<div><p>Join Amgen&rsquo;s Mission of Serving Patients</p><p>
At Amgen, if you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. Our shared mission&mdash;to serve patients living with serious illnesses&mdash;drives all that we do.</p><p>
Since 1980, we&rsquo;ve helped pioneer the world of biotech in our fight against the world&rsquo;s toughest diseases. With our focus on four therapeutic areas &ndash;Oncology, Inflammation, General Medicine, and Rare Disease&ndash; we reach millions of patients each year. As a member of the Amgen team, you&rsquo;ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.</p><p>
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you&rsquo;ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.</p><p></p><p><b>
Principal CMC Statistician</b></p><p></p><p><b>
What you will do</b></p><p>
Let&rsquo;s do this. Let&rsquo;s change the world. In this vital role you will contribute to Amgen&rsquo;s pipeline of new molecules and commercial products, that are treating serious illnesses and transforming lives.</p><p>
The Principal CMC Statistician will use their expertise to implement statistical tools and techniques with science-based practices used throughout the product life cycle. The statistician will provide multi-functional support to clinical and commercial manufacturing sites in the network including statistical support for activities such as process characterization and monitoring programs, analytical methods, specifications, and investigations.</p><p>
The statistician may also support the development of delivery devices, where they will provide statistical analysis, study designs, acceptance sampling plans and acceptance criteria for the development, qualification and transfer of physical test methods. They will also establish appropriate study designs and carry out evaluation of acceptance criteria for Design Verification testing ensuring that the overall program is aligned with Amgen and Regulatory/ISO requirements.</p><p>
Finally, the candidate will support to continuous improvement efforts across Amgen&rsquo;s networks, leading to harmonization, efficiency gains and scientific innovation and, administration of statistical training for Amgen&rsquo;s engineers and scientists.</p><ul><li><p>
Acts as a technical lead in the development, implementation and maintenance of statistical tools used to support product life cycle activities. This may include, drafting/updating white papers, writing standardized SAS and/or R code, outlining report templates, and aligning relevant SOPs.</p></li><li><p>
Provides continuous statistical support to a site or functional group by collaborating with technical associates to develop an experimental study, perform statistical analysis, and document results in a technical report that aligns with Amgen&rsquo;s document control system and has statistical integrity.</p></li><li><p>
Supports regulatory audits by interacting with technical staff to answer questions during on- site inspections; and provides written responses to clarify a statistical approach or perform additional analysis to support a Request for Information, as required.</p></li><li><p>
Participates in improvement efforts to promote statistical techniques used in biologics and monoclonal antibodies processes; and mentors and guides statistical techniques and software tools to technical associates.</p></li><li><p>
Stays up to date on biotechnology industry trends, standard processes, guidance documents and participates in external conferences, as appropriate.</p></li></ul><p></p><p><b>
What we expect of you</b></p><p>
We are all different, yet we all use our unique contributions to serve patients. The highly motivated professional we seek is a passionate individual with these qualifications.</p><p></p><p><b>
Basic Qualifications:</b></p><ul><li><p>
Doctorate Degree in Applied Statistics, Industrial Statistics or Non-clinical Biostatistics and 2 years of applied statistics experience <b>OR</b>,</p></li><li><p>
Master&rsquo;s Degree in Applied Statistics, Industrial Statistics or Non-Clinical Biostatistics and 8 to 10 years of applied statistics experience <b>OR</b>,</p></li><li><p>
Bachelor&rsquo;s Degree in Applied Statistics, Industrial Statistics or Non-Clinical Biostatistics and 10 to 14 years of applied statistics experience <b>OR</b>,</p></li><li><p>
Diploma in Applied Statistics, Industrial Statistics or Non-Clinical Biostatistics and 14 to 18 years of applied statistics experience</p></li></ul><p></p><p><b>
Preferred Qualifications:</b></p><ul><li><p>
Post-graduate degree with 6+ years&rsquo; experience in Biopharma manufacturing and control</p></li><li><p>
Proficient in statistical tools and techniques commonly used in biopharma manufacturing operations, such as, Design of Experiments, Statistical Process Control, Process Capability Analysis, Measurement System Analysis, Acceptance Sampling Plans, Non-linear and Linear Regression, Significance Tests, and Simulation.</p></li><li><p>
Proficient in SAS and/or R programming (data manipulation techniques, macro, statistical and graphical PROCs, and ODS) and JMP statistical software</p></li></ul><p></p><p><b>
What you can expect of us</b></p><p>
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being.</p><ul><li><p>
Vast opportunities to learn and move up and across our global organization</p></li><li><p>
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</p></li><li><p>
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</p></li></ul><p>
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.</p><p></p><p><b>
Apply now</b></p><p><b>
for a career that defies imagination</b></p><p>
Objects in your future are closer than they appear. Join us.</p><p><b>
careers.amgen.com</b></p><p></p><p>
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.</p><p>
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.</p><p>
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</p></div>

Principal CMC Statistician

Syneos Health

<div><p><b>Description</b>
</p>Senior Principal Statistical Programmer<p></p><p>
Syneos Health&reg; is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.</p><p>
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.</p><p></p><p>
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 accelerate the delivery of therapies, because we are passionate to change lives.</p><p></p><p>
Discover what our 29,000 employees, across 110 countries already know:</p><p></p><p><b>
WORK HERE MATTERS EVERYWHERE</b></p><p></p><p>
Why Syneos Health</p><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 our Total Self culture &ndash; where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.</li><li>
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives &ndash; we&rsquo;re able to create a place where everyone feels like they belong.</li></ul><p></p><p><b>
Job Responsibilities</b></p><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></div>

Senior Principal Statistical Programmer

Weill Cornell Medicine - Qatar

<div>
 <p>
  Job Title: Research Specialist Level 4
 </p>
 <p>
  Work Location: Qatar
 </p>
 <p>
  Organization: Research
 </p>
 <p>
  Work Days: Sunday-Thursday
 </p>
 <p>
  Sponsorship Eligibility: No
 </p>
 <p>
  Classification: Full Time
 </p>
 <p>
  <strong>
   Posting End Date: October 31st 2025
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Position Summary
  </strong>
 </p>
 <p>
  Working with little supervision from the Principal Investigator (PI), assists with study design, collection and statistical analysis of data, and interpretation and dissemination of results on various epidemiologic studies and analyses. May assist in or oversee tasks performed by less senior Lab staff. Assists and contributes in research planning, policies, and development activities procedures.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Job Responsibilities
  </strong>
 </p>
 <ul>
  <li>
   Assists with epidemiologic study design.
  </li>
  <li>
   Assists with study instruments and protocols.
  </li>
  <li>
   Performs sample size calculations and power analyses.
  </li>
  <li>
   Conducts systematic literature reviews and meta-analyses.
  </li>
  <li>
   Performs a variety of statistical analyses. Manipulates, computes, and analyzes data using statistical computer software and develops new analytical methods and testing procedures.
  </li>
  <li>
   Prepares and maintains detailed records, logs and summary reports of all data and statistical analysis charting.
  </li>
  <li>
   Prepares drafts of research plans for grant applications.
  </li>
  <li>
   Contributes to publishing research findings in scientific journals and supports presentations at medical/scientific meetings.
  </li>
  <li>
   Performs other job related duties as needed in relation to conduct of epidemiological research.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Education
  </strong>
 </p>
 <ul>
  <li>
   Bachelor's Degree in related field
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Experience
  </strong>
 </p>
 <p>
  Five or more years prior work experience or MSc/MPH in epidemiology and/or biostatistics with experience in conducting epidemiological and biostatistical research.
 </p>
 <p>
  Experience with some of the statistical packages and relevant software, such as SPSS, Stata, SAS, S-PLUS, or R.
 </p>
 <p>
  Working knowledge of epidemiology of communicable and non communicable diseases desirable.
 </p>
 <p>
  Established record of scientific research and scientific publications in peer-reviewed journals preferred.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Knowledge, Skills and Abilities
  </strong>
 </p>
 <ul>
  <li>
   Previously exhibited individual initiative.
  </li>
  <li>
   Previously demonstrated advanced proficiency in written and spoken English.
  </li>
  <li>
   Previously demonstrated advanced ability to communicate in both scientific written reports and professional presentations
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Working Conditions/Physical Demands
  </strong>
 </p>
 <ul>
  <li>
   Work is largely computer based.
  </li>
  <li>
   May require extended and varying work hours to meet demands.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Weill Cornell Medicine-Qatar was established in 2001 as a partnership between Cornell University and Qatar Foundation (QF). The first medical school in Qatar and a pioneer of coeducation at the university level, WCM-Q offers an integrated Six-Year Medical Program that incorporates pre-medical and medical studies and leads to the Cornell University M.D. degree.
 </p>
 <p>
  Teaching is by Cornell and Weill Cornell faculty, including physicians at Hamad Medical Corporation (HMC) who hold Weill Cornell appointments. Enrollment has grown rapidly from 25 first-year pre-medical students in the fall of 2002 to over 300 students from more than 30 countries today.
 </p>
 <p>
  <br/>
 </p>
 <p>
  WCM-Q is part of Weill Cornell Medicine in New York City, which was founded over 100 years ago, and shares the same mission:
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   to provide the finest education possible for medical students
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   to conduct research at the cutting edge of knowledge
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   to improve healthcare both now and for future generations
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   to provide the highest quality of care to the community
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  WCM-Q&rsquo;s home city is Doha, a thriving cosmopolitan metropolis with a culturally diverse population, a rapidly growing economy, and modern infrastructure. WCM-Q is a member of Qatar Foundation, a not-for-profit organization with multiple centers focused on education, research and innovation, and community development. WCM-Q is located within Education City, the flagship development of QF, which occupies more than 12 square kilometers and is home to some of the world&rsquo;s leading educational institutions, including Hamad Bin Khalifa University, and overseas campuses of elite universities, such as VCUarts Qatar, Texas A&amp;M University at Qatar, Northwestern Qatar, Georgetown University in Qatar, Carnegie Mellon University in Qatar, and HEC Paris in Qatar.
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  Weill Cornell Medicine-Qatar is an Equal Employment Opportunity/Minorities/Females/Disabled employer.
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</div>


Research Specialist Level 4

Aga Khan University

<div><div>Research Associate (Statistician), Paediatrics &amp; Child Health - (2500032Q)</div><div><div><br>
</div><p><b>Introduction:</b></p><p>
The Outreach and Research Programme of the Department of Paediatrics and Child Health has ten community-based field sites across Pakistan (including four in Karachi) and focuses on research for betterment of women and child health. The Department has a Nutritional Research Laboratory as well as an Infectious Disease Research Laboratory that cater to the needs of its research projects. It has well-acclaimed work to its credit both at the national and international level.</p><p>
As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment.</p><p><b>
Responsibilities:</b></p><p>
You will be responsible to analyse and interpret data from research projects; prepare descriptive tables; check data for inaccuracies; data cleaning and management and report results of statistical analyses. Specific responsibilities will be to:</p><ul><li><div>
provide statistical and analytical support to the research team</div></li><li><div>
coordinate with the project teams and independently manage all complex statistical aspects of research</div></li><li><div>
projects.</div></li><li><div>
analyze and evaluate statistical results, prepare derived datasets for the analysis using statistical</div></li><li><div>
packages like Stata, R and python</div></li><li><div>
provide Expertise in data management, data mining and prepare statistical reports with interpretation</div><div>
for manuscript publications.</div></li><li><div>
collaborate with funding agencies such as WHO and BMGF on analysis of multi-site studies</div></li><li><div>
prepare statistical contribution to Integrated Study Report;</div></li><li><div>
develop project analysis plan, including computer-generated table specifications, statistical analysis</div></li><li><div>
plan, and research report format;</div></li><li><div>
use statistical techniques and models to forecast results, trends and needs;</div></li><li><div>
prepare project summaries for weekly/monthly status meetings;</div></li><li><div>
prepare any other official assignments given by the supervisor(s)</div></li><li><div>
analyse and interpret data from research projects and prepare descriptive tables;</div></li><li><div>
check data for inaccuracies, Data Cleaning &amp; Management;</div></li><li><div>
report results of statistical analyses, including information in the form of graphs, charts, and tables;Requirements.</div></li></ul></div><div></div><div><div><br>
</div><p><b>Requirements:</b></p><p>
You should have:</p><ul><li><div>
minimum 1-2 years of experience;</div></li><li><div>
experience in the field of Research &amp; public health will be an added advantage</div></li><li><div>
4 years graduation or Masters in Statistics</div></li><li><div>
excellent Command on SPSS/Stata and other Statistical Packages;</div></li><li><div>
proficient in Spread sheets and power point presentation;</div></li><li><div>
sound knowledge of Databases and programming;</div></li><li><div>
strong verbal and written communication skills.</div></li></ul><p>
Comprehensive employment reference checks will be conducted.</p><p><b>
Disclaimer:</b></p><p>
The Aga Khan University is committed to the principles of equal employment opportunity for all employees and to providing employees with a work environment which is free from discrimination and harassment. All employment decisions at AKU are based on business needs, job requirements and individual&rsquo;s qualifications and experience, without regard to race, colour, caste or creed, national, social or ethnic origin, gender (except where gender is a bona fide occupational qualification). AKU does not discriminate among the job candidates on account of any of these characteristics.</p><div><br>
</div></div><div>
Primary Location: Pakistan-Karachi</div><div>
Organisation: Aga Khan University Pakistan</div><div>
Employee Status: Contractual</div><div>
Job Type: Experienced</div><div>
Job Posting: 24/10/2025, 4:48:30 AM</div><div>
Closing Date: 31/10/2025, 1:59:00 PM</div></div>

Research Associate (Statistician), Paediatrics & Child Health

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