research officer

ux researcher

research

مجموعة الموسى الصحية

<div><p><b>Duties and Responsibilities:
</b></p><p>&middot; R esponsibilities include coordination and close monitoring of research projects.
</p><p>&middot; Assisting in the progress of project deliverables and studies&rsquo; implementation.
</p><p>&middot; Responsible for providing moderate to advanced range of coordination of Research studies conducted at ASH.
</p><p>&middot; Works under general direction of the research center director.
</p><p>&middot; Responsible for research-related tasks (organization, editing/writing related to project deliverables including research reports, manuscripts and proposals).
</p><p>&middot; Establishes liaisons with relevant parties at ASH that may include: doctors, medical technicians, nurses and clinical information system.
</p><p>&middot; Assists with the recruitment and enrollment of studies&rsquo; participants, research data collection and other required study coordination activities.
</p><p>&middot; Regular, professional communication with assigned project teams.
</p><p>&middot; Ensures accurate execution of research protocols in accordance with Good Clinical Practices (GCP), and local and international obligations to patients.
</p><p>&middot; Interfaces directly with patients/subjects and Principal Investigators.
</p><div>&middot; Drafts posters and abstracts for research center events.
</div><div>&middot; Conducts literature reviews for proposals and manuscripts.
</div><div>&middot; Performs other related research duties as assigned.
</div><p><b>Qualifications:
</b></p><p>&middot; Bachelor in statistics, mathematics or health related sciences, with excellent training in research methodology and biostatistics.
</p><p>&middot; Research coordinator certificate
</p><p>&middot; GCP certificate
</p><p><b>Professional experience:
</b></p><p>&middot; Bachelor degree with at least 2 years&rsquo; experience in research coordination.
 </p><p><b>Specialized skills </b>:
</p><p>&middot; Strong knowledge in research methodology, GCP and research ethics.
</p><p>&middot; Ability to work independently and as part of a team and self-motivated.
</p>Ability to multi-task and to prioritize competing demands efficiently with minimal supervision to meet deadlines.</div>

Research Officer

Tasheel Law Firm

<p><b>Role Overview:</b><br/>The Market Research Analyst will support strategic decision-making by conducting in-depth market analysis, industry research, and competitive intelligence. The role requires strong analytical capabilities, business acumen, and the ability to translate data into actionable insights.</p><p><b>Key Responsibilities:</b></p><ul><li>Conduct comprehensive market research, including industry analysis, market sizing, and trend assessment.</li><li>Gather and analyze data on competitors, customers, and market dynamics to identify opportunities and risks.</li><li>Develop detailed reports, dashboards, and insights to support business strategy and investment decisions.</li><li>Perform benchmarking and comparative analysis across sectors and geographies.</li><li>Support feasibility studies, business plans, and strategic advisory engagements.</li><li>Collaborate with internal teams to align research outputs with client requirements and project objectives.</li><li>Monitor economic, regulatory, and sector-specific developments impacting the market.</li><li>Utilize research tools, databases, and analytical frameworks to ensure high-quality outputs.</li></ul><p><b>Preferred Skills &amp; Qualifications:</b></p><ul><li>Strong analytical and problem-solving skills with attention to detail.</li><li>Proficiency in research methodologies and data analysis tools.</li><li>Advanced skills in <b>Microsoft Excel and PowerPoint</b>; ability to create <b>high-quality, client-ready presentations</b> is a strong advantage.</li><li>Experience in preparing <b>PowerPoint presentations, reports, and pitch decks</b> will be considered a plus.</li><li>Excellent written and verbal communication skills.</li><li>Prior experience in consulting, advisory, or research roles is preferred.</li></ul><p><b>Engagement Type:</b><br/>Full-time role based in Riyadh, Saudi Arabia.</p><p>Job Type: Full-time</p>

Market Research Analyst - Female

KAUST (King Abdullah University of Science and Technology)

<div>
 <p>
  <strong>
   The Role
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Research Compliance Specialist is responsible for creating, developing, implementing, and promoting the Research Data Management (RDM) Program at KAUST. RDM training and management provide the foundation for the preservation, protection, and monetization of one of KAUST&rsquo;s most valuable resources (research data).
 </p>
 <p>
  <br/>
 </p>
 <p>
  KAUST is an internationally respected research institution, and its reputation is dependent upon the good data management practices of its researchers.
 </p>
 <p>
  <br/>
 </p>
 <p>
  A state-of-the-art RDM program developed and implemented by the Research Compliance Specialist will ensure that the University conducts research that meets or exceeds national and international RDM standards. By enabling the reuse of data and rationalizing resource allocation, RDM supports both research excellence and the optimization of operating costs. In addition, the reputation of the University is impacted by the RDM practices that its graduates and postdoctoral researchers take with them when they leave the University.
 </p>
 <p>
  The Research Compliance Specialist will ensure that the University&rsquo;s students and postdoctoral
 </p>
 <p>
  researchers leave KAUST adequately equipped to manage research data.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Serve as a subject matter expert on research data management (RDM) regulations, guidelines, and best practices.
  </li>
  <li>
   Promote a culture of responsible research data management across KAUST&rsquo;s diverse research environment.
  </li>
  <li>
   Analyze existing RDM systems and processes, identifying gaps and opportunities for integration.
  </li>
  <li>
   Develop and implement policies governing RDM at the University.
  </li>
  <li>
   Design, deploy, and manage RDM tools or solutions tailored to KAUST&rsquo;s needs.
  </li>
  <li>
   Coordinate and consolidate existing guidance, resources, and efforts across departments.
  </li>
  <li>
   Benchmark with external institutions and stakeholders to identify RDM best practices.
  </li>
  <li>
   Prepare guidance documents, online resources, and web content to support RDM practices.
  </li>
  <li>
   Provide strategic advice to stakeholders on implementing effective RDM practices.
  </li>
  <li>
   Develop course curricula and deliver training sessions, workshops, and presentations on RDM.
  </li>
  <li>
   Engage with faculty, staff, students, and administrators to foster compliance and awareness.
  </li>
  <li>
   Monitor, audit, and evaluate the effectiveness of the RDM program.
  </li>
  <li>
   Assist with investigations or enquiries related to alleged RDM mismanagement.
  </li>
  <li>
   Perform day-to-day administrative duties associated with the RDM program.
  </li>
  <li>
   Provide administrative support to other compliance programs, including: Animal Care and Use, Biosafety, Human Subjects Research, Radiation Safety, Scientific Diving, and Responsible Conduct of Research Programs.
  </li>
  <li>
   Be cross-trained and able to assist colleagues in the support of the above programs.
  </li>
  <li>
   Supplement administration of Research Compliance and RCR activities.
  </li>
  <li>
   Transcribing notes, minutes, and formal proceedings.
  </li>
  <li>
   Other duties as assigned.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Doctoral or master&rsquo;s degree in a regulatory, scientific or related field.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Required Skills
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   6+ years of research data management experience within a scientific or related environment.
  </li>
  <li>
   Experience with RDM program administration is preferred.
  </li>
  <li>
   Customer-driven approach.
  </li>
  <li>
   Demonstrated expertise in RDM practices.
  </li>
  <li>
   Proactive and self-driven.
  </li>
  <li>
   Strong organizational skills.
  </li>
  <li>
   Collaborative nature with strong persuasive skills.
  </li>
  <li>
   A firm understanding of scientific practices and research methods.
  </li>
  <li>
   Knowledge of organizational and administrative support processes.
  </li>
  <li>
   Strong verbal and written communication skills.
  </li>
  <li>
   Demonstrated proficiency with computer applications.
  </li>
  <li>
   Excellent verbal, written communication, and presentation skills.
  </li>
  <li>
   High degree of confidentiality.
  </li>
 </ul>
 <p>
 </p>
</div>


Research Data Management Compliance Specialist

State Street

<div><div><b>Who we are looking for</b></div><div>
This role is for a Quantitative Research Analyst in the Systematic Equity team. The role is based in Riyadh and reports to the Lead Research Supervisor of Systematic Equity.</div><div></div><div>
Systematic Equity team manages a wide range of quantitative equity strategies over a broad active risk spectrum across global markets. The team has a deep history of delivering innovative risk-controlled alpha to our clients and we are looking for someone who can help shape the next phase of our growth with extraordinary analytical skills and passion for data science. You will have an opportunity to combine your analytical skills and investment insights with innovative data and modeling techniques on a cutting-edge distributed computing platform to solve investment problems.</div><div></div><div><b>
Why this role is important to us</b></div><div>
The team you will be joining is a part of State Street Investment Management, one of the biggest asset managers in the world, that provides services to the world&rsquo;s governments, institutions and financial advisors across the globe. With over four decades of experience and trillions of dollars in assets under management, we offer one of the broadest selections of services across asset classes, risk profiles, regions and styles. As pioneers in index, ETF, and ESG investing, we are always inventing new ways to invest. Join us if making your mark in the asset management industry from day one is a challenge you are up for.</div><div></div><div><b>
What you will be responsible for</b></div><ul><li>
Generate ideas for investment process innovation and improvements with key focus in alpha generation and portfolio construction.</li><li>
Execute research projects including interpreting, presenting and implementing results.</li><li>
Contribute to maintaining and improving our state-of-the-art computing platform for research and production models.</li><li>
Explore and evaluate alternative data sources and machine learning techniques to solve investment problems better.</li></ul><div></div><div><b>
Education &amp; Preferred Qualifications</b></div><ul><li>
Advanced degree (PhD/MS or equivalent) in finance, economics or a quantitative discipline such as computer science, mathematics, statistics, physics or engineering.</li><li>
Minimum 2 years of work experience in quantitative finance.</li><li>
Deep knowledge of quantitative equity investments.</li><li>
Great analytical skills with solid knowledge in statistics.</li><li>
Strong problem solving capabilities with attention to details.</li><li>
Excellent coding skills with experience in Python and/or SQL. Experience with distributed computing is a plus.</li><li>
Strong working knowledge of theoretical and practical concepts in machine learning including natural language processing.</li><li>
Experience working with a large amount of structured/unstructured data is a plus.</li></ul><div></div><div><b>
About State Street</b></div><div></div><div>
Across the globe, institutional investors rely on us to help them manage risk, respond to challenges, and drive performance and profitability. We keep our clients at the heart of everything we do, and smart, engaged employees are essential to our continued success.</div><div></div><div>
We are committed to fostering an environment where every employee feels valued and empowered to reach their full potential. As an essential partner in our shared success, you&rsquo;ll benefit from inclusive development opportunities, flexible work-life support, paid volunteer days, and vibrant employee networks that keep you connected to what matters most. Join us in shaping the future.</div><div></div><div>
As an Equal Opportunity Employer, we consider all qualified applicants for all positions without regard to race, creed, color, religion, national origin, ancestry, ethnicity, age, disability, genetic information, sex, sexual orientation, gender identity or expression, citizenship, marital status, domestic partnership or civil union status, familial status, military and veteran status, and other characteristics protected by applicable law.</div><div></div><div>
Discover more information on jobs at <div>StateStreet.com/careers</div></div><div></div><div>
Read our <div>CEO Statement</div></div></div>

Quantitative Research Analyst, Systematic Equity - AVP

CTI Clinical Trial and Consulting

<div><div><b>Clinical Research Associate (level dependent on experience)</b><br>
<br>
<b>Job Purpose/Summary</b></div>
<div><br>
As a CRA you will be responsible for the successful conduct of clinical trials and serve as the main contact for the investigative site by representing CTI in a professional manner.</div>
<div></div><div><b>What You&rsquo;ll Do</b></div>
<ul><li>Conduct evaluation, initiation, monitoring and close out visits</li>
<li>Assist with regulatory and study start-up activities including contract and budget negotiations</li>
<li>Ensure clinical data integrity and meet study timelines</li>
<li>Provide ongoing updates and support to project management</li>
<li>Attend global project meetings including investigator meetings and global team teleconferences</li>
<li>Complete assigned training programs in drug development processes, therapeutic areas, Good Clinical Practices (GCPs) and any applicable local regulatory requirements.</li>
</ul><div><b>What You Bring</b></div>
<ul><li>2 - 3 years of clinical research experience as a CRA or related profession</li>
<li>Life science background</li>
<li>Excellent knowledge in ICH-GCP and regulatory requirement</li>
<li>Fluent in English</li>
</ul><div><b>Why CTI?</b></div>
<div>At CTI, we recognize that our people are what make our company successful. Our work moves medicine forward.</div>
<div></div><div>For that reason, we treat our team members with the respect they deserve, and our numbers show it:</div>
<ul><li>We support career progression &ndash; We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward</li>
<li>We value education and training &ndash; We provide tuition assistance, partner with universities and colleges to create programs in our field, and have a dedicated training department</li>
<li>We value our people - We have never had a layoff in our three decade history and we guaranteed full pay for our employees during the COVID-19 shut-down regardless of the number of hours worked. We support a work-life balance and the importance of time with family by offering generous vacation time, a hybrid work from home schedule, and paid parental leave.</li>
<li>Our culture is unparalleled &ndash; We've received multiple awards recognizing CTI as one of the best places to work in the greater Cincinnati area, as well as one of the top CROs in the industry</li>
<li>We think globally and act locally &ndash; With employees across 60 countries, we have global reach but maintain culture and connections to the local communities in which we work. Our CTI Cares Committees are dedicated to ensuring the CTI culture and values translate around the world.</li>
<li>We are looking toward the future &ndash; We have had a consistent double-digit growth rate over the last decade, invest in cutting-edge technology, and pride ourselves on our average annual retention rate of 95%, which is much higher than many other CROs</li>
<li>Our work makes a difference &ndash; We focus our work on treatments for chronically and critically-ill patients, who are depending on us to bring these life-changing therapies to market</li>
</ul><div><div><div><div>Are you interested? Then we look forward to your electronic application, with a tabular CV in English.<br>
<br>
<b>CTI Clinical Trial and Consulting Services</b><br>
<br>
Filipa Magalh&atilde;es<br>
<br>
www.ctifacts.com</div></div></div></div></div>

Clinical Research Associate (level dependent on experience)

Blue Book Global

<div><div>Blue Book Global</div><div>
Saudi</div><div>
Mid</div></div>
<br><div><div><div><div><h2 class="jobSectionHeader"><b>About the Role</b></h2><p>
A leading UX agency is seeking a UX Researcher to deliver meaningful insights for clients across Saudi Arabia. This is your opportunity to shape how people experience digital products at scale.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
What You'll Do</b></h2><ul><li>
Conduct user research to understand behaviours, motivations, and pain points across multiple industries</li><li>
Lead qualitative and quantitative research including interviews, surveys, usability testing, and ethnographic studies</li><li>
Collaborate with UX designers, product managers, and developers to turn findings into actionable design recommendations</li><li>
Benchmark user experiences against local and international best practices</li><li>
Deliver compelling reports and presentations that communicate insights and strategic opportunities</li><li>
Work closely with stakeholders to influence meaningful product and service improvements</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What We Need</b></h2><ul><li>
Proven experience in UX research</li><li>
Strong knowledge of research methodologies, data analysis, and user testing techniques</li><li>
Ability to distil complex information into clear, actionable insights</li><li>
Excellent communication and presentation skills</li><li>
Fluent in both Arabic and English</li><li>
Based in Saudi Arabia or willing to relocate</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
What You'll Get</b></h2><ul><li>
Shape digital experiences for leading brands in Saudi Arabia</li><li>
Work with a team of UX experts driving user-centered design</li><li>
Gain exposure to cutting-edge projects across various industries</li><li>
Competitive package</li></ul></div></div></div></div><p></p>

UX Researcher

<div>
 <p>
  <strong>
   The Role
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Staff Scientist in the Viral Vector Facility (VVF) plays a central role in supporting the strategic goals of the Bio-Medical platform. The Scientist in the VVF will design, produce, and deliver high-quality viral vectors (e.g., AAVs and Lentivirus) to support cutting-edge research at KAUST and in the region. The scientist will optimize and scale production workflows, improve vector performance and cost-efficiency, and ensure strict quality and biosafety standards. We are seeking a highly skilled molecular biologist with expertise in viral vector engineering and production, who can translate complex experimental needs into tailored genetic tools and drive innovation in vector design and delivery. The scientist will collaborate closely with researchers, supervise technical staff, and provide advanced training in molecular genetics and viral vector technologies, helping position KAUST as a regional hub for state-of-the-art viral vector solutions.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Responsibilities
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   <strong>
    Scientific Collaboration:
   </strong>
   Collaborate with researchers to identify appropriate viral vector systems that address key scientific questions, supporting high-impact research and publications.
  </li>
  <li>
   <strong>
    Viral Vector Production:
   </strong>
   Produce high-quality, safe, and effective viral vectors tailored to experimental needs and cell-based research applications.
  </li>
  <li>
   <strong>
    Staff &amp; Operations Management:
   </strong>
   Supervise and mentor a laboratory technician; manage daily tasks to ensure timely and high-quality work deliverables.
  </li>
  <li>
   <strong>
    Project management:
   </strong>
   Coordinate multiple research projects and timelines to ensure milestones and deliverables are met on schedule.
  </li>
  <li>
   <strong>
    SOP Development &amp; Maintenance:
   </strong>
   Develop, implement, and enforce standard operating procedures (SOPs) to ensure efficiency, reproducibility, and compliance in viral vector production.
  </li>
  <li>
   <strong>
    Laboratory Safety &amp; Compliance:
   </strong>
   Ensure Good Laboratory Practice (GLP) and maintain a safe working environment in accordance with biosafety regulations and Institutional Biosafety and Ethics Committee (IBEC) guidelines.
  </li>
  <li>
   <strong>
    Data Integration &amp; Collaboration:
   </strong>
   Integrate laboratory data into the Bio-Medical Platform and collaborate with IT and bioinformatics teams for effective data management, analysis, and reporting.
  </li>
  <li>
   <strong>
    Process Innovation:
   </strong>
   Design and implement new or improved techniques and workflows to address scientific challenges, enhance viral vector performance and throughput, and reduce production costs.
  </li>
  <li>
   <strong>
    Training &amp; Knowledge Development:
   </strong>
   Provide advanced training in viral vector production and contribute to building technical expertise among staff.
  </li>
  <li>
   <strong>
    General Laboratory Duties:
   </strong>
   Conduct routine laboratory responsibilities, including procurement, documentation, equipment maintenance, and participation in task forces and institutional committees.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   A PhD degree in relevant field
  </li>
  <li>
   5-7 + years of hands-on experience in molecular genetics, cloning, gene editing, viral vector production, cell culture.
  </li>
  <li>
   Strong scientific track records, including successful management of research projects, and/or demonstrated operational excellence, and/or publication in high-impact peer-reviewed journals.
  </li>
 </ul>
 <p>
 </p>
 <p>
  <strong>
   Required Skills
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   In-depth knowledge and strong expertise in cell and molecular genetics.
  </li>
  <li>
   Proven experience in the production of viral vectors (such as AAVs, Lentiviruses, Rabies Virus etc.) and gene manipulation technologies.
  </li>
  <li>
   Experience in primary human cell immortalization.
  </li>
  <li>
   Demonstrated ability to collaborate with researchers in the biological sciences, understand their experimental needs, and translate these into effective genetic tools.
  </li>
  <li>
   Excellent organization skills with a proven ability to manage and execute multiple research projects simultaneously.
  </li>
  <li>
   Strong written and verbal communication skills, with the ability to engage with stakeholders and foster a collaborative work environment.
  </li>
  <li>
   A proactive, results-driven team player with a commitment to achieving shared goals.
  </li>
 </ul>
 <p>
 </p>
</div>


Viral Vector Staff Scientist

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