associate researcher Jobs in Saudi Arabia

associate researcher

research and development manager Jobs in Saudi Arabia

research and development manager

research and development scientist Jobs in Saudi Arabia

research and development scientist

researcher

research

Alfaisal University

<div></div><div><div><h5 class="jobSectionHeader"><b>Overview</b></h5>
<div></div><div><div><div>Department<b> College of Science</b></div>
</div><div></div><div><div>Division<b>All College Disciplines
</b></div></div></div><div></div><div><div><div>Job Family<b>Faculty- Academic</b></div>
</div><div></div><div><div>Reports to<b>Director of the Department</b></div>
</div></div><div></div><div><div><div>Location<b>Alfaisal University - Riyadh
</b></div></div></div></div><div><h4 class="jobSectionHeader"><b>Job Summary</b></h4>
<p>The Research Assistant provides technical, operational, and administrative support for laboratories and research activities across the university. The role involves assisting with research projects, maintaining lab equipment and supplies, supporting faculty and student research, implementing lab safety procedures, and contributing to the development and documentation of research outputs. The position is designed to ensure efficient and compliant lab operations that facilitate high-quality research and learning environments. The research Assistant also implements lab safety policies and procedures and handles all administrative aspects of the labs.</p>
<p><b>Primary Duties &amp; Responsibilities</b></p>
<ul><li>Supports research projects by preparing materials, assisting in experiments, and collecting and organizing data as directed by research faculty or lab heads to ensure smooth research progress.</li>
<li>Supervises and assists students and junior staff during laboratory sessions, ensuring adherence to lab protocols and safety standards to maintain a safe learning environment</li>
<li>Performs routine laboratory duties including maintaining equipment, managing supplies and inventory, and handling basic troubleshooting and maintenance to ensure lab readiness.</li>
<li>Implements and ensures compliance with lab safety policies and procedures; conducts regular self-inspections to maintain a safe research environment and control hazards.</li>
<li>Maintains accurate records of lab activities, equipment maintenance, and research documentation to support traceability and accountability.</li>
<li>Provides technical guidance and training to staff and students on proper laboratory techniques and safety protocols to enhance competence and safety.</li>
<li>Participates in professional development activities to stay current with advancements in laboratory procedures and research methodologies, ensuring up-to-date practices.</li>
<li>Assists with administrative aspects of lab operations, including scheduling, procurement, and documentation for audits or accreditations to support operational efficiency.</li>
<li>Contributes to the preparation of research-related documentation such as reports, articles, and grant support materials to facilitate knowledge sharing and funding.</li>
<li>Maintains regular availability for consultation and support to faculty, students, and collaborators involved in research or lab-based coursework to foster collaboration and problem-solving.</li>
<li>Performs all duties in a professional, effective, and confidential manner.</li>
<li>Performs all other related duties as required or assigned by the manager.</li><br>
</ul><br>
<h4 class="jobSectionHeader"><b>Education &amp; Experience</b></h4>
<ul><li>Bachelor's degree in a scientific or health-related field (e.g., Science, Biomedical Sciences, Pharmacy, Engineering or related field from accredited institute.</li>
<li>Minimum of three (03) years of experience in research, laboratory environment institution or related fields.
</li></ul><br>
<b>Please upload CV in ENGLISH ONLY</b></div></div><p></p>

Research Assistant

Confidential Company

<div>
 <p>
  <strong>
   Position Summary:
  </strong>
 </p>
 <p>
  We are seeking a highly skilled and motivated PhD-level R&amp;D Scientist with 3&ndash;4 years of experience in drilling fluid systems and simulation modeling. The ideal candidate will lead and contribute to the development and optimization of advanced drilling fluid technologies and digital simulation tools to enhance wellbore stability, efficiency, and sustainability in drilling operations.
 </p>
 <p>
  This is a strategic role for someone who combines deep technical knowledge with hands-on experience in lab research, fluid rheology, and numerical modeling.
 </p>
 <p>
  <strong>
   Key Responsibilities:
  </strong>
 </p>
 <ul>
  <li>
   Lead and conduct R&amp;D projects focused on designing, testing, and improving drilling fluid systems (water-based, oil-based, synthetic-based, or polymer-based).
  </li>
  <li>
   Develop and implement simulation models (e.g., hydraulics, thermal modeling, cuttings transport, fluid loss) to predict drilling fluid performance in various well conditions.
  </li>
  <li>
   Utilize numerical tools (e.g., ANSYS, COMSOL, CFD, or custom simulators) to optimize formulations and drilling parameters.
  </li>
  <li>
   Conduct laboratory experiments to assess rheology, stability, filtration, and other key drilling fluid properties under HPHT conditions.
  </li>
  <li>
   Analyze experimental and field data to correlate simulation models with real-world performance.
  </li>
  <li>
   Collaborate with field engineers, product development teams, and clients to troubleshoot field challenges and deliver customized fluid solutions.
  </li>
  <li>
   Write technical reports, research papers, and contribute to patent filings and conference presentations.
  </li>
  <li>
   Stay updated on emerging technologies, materials, and digital innovations in drilling and well construction.
  </li>
 </ul>
 <p>
  <strong>
   Required Qualifications:
  </strong>
 </p>
 <ul>
  <li>
   PhD in Chemistry , Petroleum Engineering, Chemical Engineering, or a related field with a specialization in drilling fluids ..
  </li>
  <li>
   3&ndash;4 years of industry or academic R&amp;D experience focused on drilling fluid systems and simulation.
  </li>
  <li>
   Strong knowledge of fluid rheology, wellbore hydraulics, HPHT testing, and formation interactions.
  </li>
  <li>
   Strong problem-solving abilities and capability to design and conduct structured research programs.
  </li>
  <li>
   Excellent written and verbal communication skills, including the ability to present technical findings to both technical and non-technical audiences
  </li>
 </ul>
 <p>
 </p>
</div>


Research And Development Scientist

Tahcom

<p>Lead and manage the R&amp;D function to drive innovation, oversee AI product development, and ensure alignment with the company&rsquo;s strategic goals. Foster a high-performance research culture and ensure the successful commercialization of AI solutions.</p><p><b>Key Responsibilities</b></p><ul><li>Strategic Leadership</li><li>Develop and implement the R&amp;D strategy in line with business objectives and the GCC&rsquo;s innovation vision.</li><li>Identify and prioritize AI research areas with high commercial and societal impact.</li><li>Project &amp; Team Management:</li><li>Lead, mentor, and grow a multidisciplinary team of AI researchers, data scientists, and engineers.</li><li>Oversee all R&amp;D projects, ensuring timely delivery, quality, and budget adherence.</li><li>Innovation &amp; Collaboration:</li><li>Foster a culture of continuous innovation and learning.</li><li>Collaborate with cross-functional teams (product, engineering, marketing, business development).</li><li>Build partnerships with universities, research centers, and industry bodies in the GCC.</li><li>Compliance &amp; Reporting:</li><li>Ensure all R&amp;D activities comply with local and international regulations, including data privacy and AI ethics.</li><li>Prepare and present regular reports on R&amp;D progress, risks, and outcomes to executive leadership.</li><li>Technology &amp; Market Awareness:</li><li>Stay updated on global AI trends, emerging technologies, and competitor activities.</li><li>Evaluate and integrate new tools, frameworks, and methodologies relevant to AI.</li><li><b>Education:</b></li><li>Master&rsquo;s or PhD in Computer Science, Artificial Intelligence, Data Science, Engineering, or a related field.</li><li><b>Experience:</b></li><li>+7 years in R&amp;D roles, with at least 3 years in a managerial or team lead capacity.</li><li>Proven track record in AI/ML research, product development, or deployment.</li><li>Experience in the GCC or emerging markets is a strong plus.</li><li>Technical Skills:</li><li>Deep understanding of AI/ML algorithms, data engineering, and cloud platforms.</li><li>Familiarity with AI ethics, data privacy, and regulatory frameworks in the GCC.</li><li>Experience with project management tools and agile methodologies.</li><li>Leadership &amp; Soft Skills:</li><li>Strong leadership, team-building, and mentoring abilities.</li><li>Excellent communication and stakeholder management skills.</li><li>Strategic thinker with strong problem-solving and decision-making capabilities.</li><li>Ability to work in a multicultural, fast-paced startup environment.</li></ul><p>Job Type: Full-time</p><p>Pay: &#65020;5,000.00 - &#65020;7,500.00 per month</p>

Research and Development Manager

Raytheon

<div><p><b>Date Posted:</b></p>
2025-04-20<p><b>
Country:</b></p>
Saudi Arabia<p><b>
Location:</b></p>
SAU02114: MTSD AlAndalus, 3267 Corniche Street, Al Andalus District, Jeddah, 02, 23311-9520, Saudi Arabia<p><b>
Position Role Type:</b></p>
Unspecified<p></p><p><b>
Job Title</b>: <b>Patriot Data Research Analyst Job Code/Profile: ENGSVEP2</b></p><p><b>
Salary Grade</b>: P2<br>
<b>Job Location:</b> Jeddah, KSA</p><p><b>
Field Manager:</b> <b>Robert Ruder</b></p><p><b>
Cost Center:</b> 25640</p><p></p><p>
At Raytheon, the foundation of everything we do is rooted in our values and a higher calling &ndash; to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today&rsquo;s mission and stay ahead of tomorrow&rsquo;s threat. Our team solves tough, meaningful problems that create a safer, more secure world.</p><p></p><p><b>
Job Summary</b></p><p></p><p>
The Patriot Data Research Analyst position is a critical role supporting the sustainment of Royal Saudi Air Defense Forces (RSADF) systems through meticulous inventory management and data analysis. The analyst is responsible for reviewing and verifying materials within the inventory control point stock, as well as tracking materials received under requisitions and spare parts orders to address shortages. This role involves maintaining and updating the master inventory records file, ensuring accuracy and reliability in stock data. The analyst assists with stock-gathering activities, including evaluating the feasibility of substitutions and exchanges, and supports the development and maintenance of spare parts database requirements. Through detailed inventory analysis and research, the analyst identifies trends, resolves discrepancies, and prepares responses to problem reports concerning spare parts shortages from suppliers. The role also involves analyzing Repair and Return (R&amp;R) materials and replenishment procedures, making recommendations to management to optimize processes and enhance operational readiness. Additionally, the analyst contributes to on-the-job training (OJT) initiatives to share expertise and foster professional development within the team. By performing these critical tasks, the Patriot Data Research Analyst ensures the effective management of inventory and the sustainment of RSADF systems. This position requires strong analytical skills, attention to detail, and a commitment to excellence in inventory and data management.</p><p></p><p>
This position is based in Jeddah, Saudi Arabia.</p><p></p><p><b>
What You Will Do</b></p><p></p><ul><li>
Review and confirm the materials in the inventory control point stock and the materials</li></ul><p>
received under requisitions and spare parts orders to replenish shortage.</p><ul><li>
Maintain master inventory records file.</li><li>
Assists in stock-gathering activities and decisions about the possibility of substitution and</li></ul><p>
Exchange.</p><ul><li>
Assist in the preparation of spare parts database requirements and the subsequent inventory,</li></ul><p>
analysis and research.</p><ul><li>
Participate in On-the-Job Training (OJT) when needed.</li><li>
Review and prepare responses to problem reports with spare parts to replenish shortage</li></ul><p>
from suppliers.</p><ul><li>
Analyzes and makes recommendations to management for Repair and Return (R&amp;R)</li></ul><p>
materials and replenishment procedures.</p><p></p><p><b>
Qualifications You Must Have</b></p><p></p><ul><li>
Diploma in Logistics or Supply from an accredited foreign or local college or institute.</li><li>
Minimum of two (2) years prior experience in Logistics or Supply or compatible experience in the operation of industrial and military supply activities.</li><li>
Able to explain and interpret technical manuals and drawings as they apply to supply activities.</li><li>
Proficient in the use of computer and database.</li><li>
Proficient in spoken and written English.</li><li>
Must be able to work independently.</li></ul><p><b>
What We Offer</b></p><p></p><ul><li>
Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Trust, Respect, Accountability, Collaboration, and Innovation.</li></ul><p></p><p><b>
Learn More &amp; Apply Now!</b></p><p></p><ul><li>
RTX solves some of the toughest challenges in aerospace and defense. That requires expansive thinking and bold innovation &ndash; and that, in turn, requires a culture that is diverse, equitable and inclusive.</li><li>
We embrace individuality and diversity of thought to fuel opportunity for our employees, our customers, and our communities. We work toward progress, knowing that a more inclusive world is critical to our mission. Not just in this moment, but always.</li></ul><p></p><p><b>
Please consider the following role type definition as you apply for this role.</b></p><p></p><ul><li><b>
Onsite:</b> Employees who are working in Onsite roles will work primarily onsite.</li></ul><p></p><p><b>
Clearance Information</b></p><p></p><ul><li>
This position requires a security clearance from the Royal Saudi Air Defense Forces.</li></ul><p></p><p><i>
RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law.</i>
</p><p></p><p><b>Privacy Policy and Terms:</b></p><p>
Click on this link to read the Policy and Terms</p></div>

Patriot Data Research Analyst

<div><p>Job Description</p><p></p><p>
This role combines the accountability of a clinical research manager and certain elements of a GCTO country lead role. Holders of this position are accountable for:</p><ul><li>
The performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Our company&rsquo;s policies and procedures, quality standards and adverse event reporting requirements internally and externally</li><li>
Under the oversight of the CRD, providing leadership to a country: liaising with local country Management team, participating in the local medical governance and providing oversight for the GCTO team in the country serving as a primary point of contact for managing clinical trial execution in all its aspects across phases I/II through III/IV in that country It could include line management of the GCTO our company's employees if required</li></ul><p></p><p>
Responsibilities include, but are not limited to:</p><p></p><p>
CRM component ( Minimum of 50% of time expected to be project related, to be defined according to the need):</p><ul><li>
Point of Contact (POC) for assigned protocols between Country Operations (CO) and clinical trial team (CTT) ( or ROC where applicable)</li><li>
Pro-actively drives/tracks execution and performance of deliverables/timelines/results to meet country commitments for assigned protocols. Strong collaboration with local CO roles. Forecasts country resource needs. Serves local business needs (signs contracts, manages budgets as delegated).</li><li>
Responsible for quality and compliance in assigned protocols in country in close collaboration with CRAs and local study team. Reviews Monitoring Visits Reports and Escalates performance issues and training needs to CRA manager and/or functional vendor and internal management as needed.</li><li>
Responsible for collaboration with functional outsourcing vendors, investigators, other external partners. Oversees country and site validations, site selection and recruitment in assigned protocols. Responsible for clinical trial education to sites. Country POC for programmatically outsourced trials for assigned protocols.</li><li>
Collaborates internally with local PV, Regulatory, GMA/GHH to align on key decisions in his/her studies. Significantly impacts on the ability to effectively conduct clinical studies and develop the pipeline, while maintaining local regulatory and compliance requirements in countries. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives. As a customer-facing role, this position will build business relationships and represent our company's with investigators, functional outsourcing partners and other external partners and therefore have a significant impact on country-level customer relationships.</li><li>
Oversee country commitments, compliance and training needs. Additionally, business leadership and alignment with corporate requires that individual has ability to lead across several dimensions simultaneously.</li><li>
Works collaboratively with Country, Regional and HQ Operations; Pharmacovigilance, Regulatory, Global Medical Affairs and Global Human Health internally; and with external functional outsourcing vendors. Requires coordination and alignment with the regional and broader organization. Additionally, will work to build and maintain relationships with investigators and other external partners and promote the company reputation. In collaboration with CRD and/or CRM manager represents our company's in Pharma industry issues and in seeking influence in external R&amp;D environment.]</li></ul><p>
Country Lead component (% of time to be defined according to the needand always less than 50% or less than 25% if no line management is included.)</p><ul><li>
Work collaboratively in a matrix organization with all groups within GCTO, especially with Clinical Sciences and Study Management (CSSM), Clinical Quality Managers (CQMs), to deliver objectives.</li><li>
Collaborate with Functional Service Provider (FSP) local Leadership to ensure adequate and appropriate resourcing for the Our company&rsquo;s internal clinical trial portfolio</li><li>
Collaborate with Clinical Research Organization (CRO) local Leadership to ensure the successful implementation of fully-outsourced clinical trials</li><li>
Represents GCTOin the Medical Governace council.</li><li>
Support the development and management of Investigator relationships in conjunction with the OUR RESEARCH &amp; DEVELOPMENT DIVISION Therapy Areas, and when appropriate, Human Health colleagues. Contribute to the program life-cycle management through effective study allocation and execution (prioritizing programs, working with KOLs, etc.).</li><li>
Take responsibility for any subsidiary clinical audits, working closely with the Quality Assurance (QA) group and the Good Clinical Practice Quality and Compliance Council (GCP QCC).</li><li>
Represents the GCTO organization both internally and externally within the industry in the country.</li><li>
Represents GCTO in the local subsidiary management team ( could be extended leadership team)</li><li>
In case of line manager of GCTo staff:</li></ul><p>
o Responsible for ensuring appropriate scientific and operational training for staff members.<br>
o Effectively manage resources to ensure appropriately skilled and high performing staff members are assigned to support the effective execution of the portfolio and achieve GCTO, GCD, and OUR RESEARCH &amp; DEVELOPMENT DIVISION objectives. Sets clear performance standards and holds self and organization accountable for achieving results. Embraces GCTO metrics and performance standards (KPI&rsquo;s)</p><p></p><p>
CORE Competency Expectations:</p><ul><li>
Knowledge in Site Management.</li><li>
Strong organizational skills with demonstrated success required.</li><li>
Requires ability to make decisions independently and oversee important activities relevant to clinical research activities in the country according to predetermined global policies and commitments with the support, oversight and supervision of the CRM Manager or CRD</li><li>
Requires strong understanding of local regulatory environment for the individual to weigh</li><li>
pros and cons of key decisions with input from manager.</li><li>
Strong scientific and clinical research knowledge is required for this position.</li><li>
Strong understanding of clinical trial planning, management and metrics is essential as well as the ability to focus on multiple deliverables and protocols simultaneously.</li><li>
Ability to collaborate with different stakeholders within GCTO and OUR RESEARCH &amp; DEVELOPMENT DIVISION in a matrix organization.</li><li>
Ability and skills to manage resource allocation, processes (and controls), productivity, quality and project delivery</li><li>
Strong Communication skills requiring proficiency in written and spoken English and local language. The incumbent must be competent and effective in written and verbal communication.</li><li>
Strategic thinking</li></ul><p>
Behavioral Competency Expectations:</p><ul><li>
High emotional intelligence</li><li>
Leadership skills that enable and drive alignment with the goals, purpose and mission of Our company&rsquo;s Research Labs (OUR RESEARCH &amp; DEVELOPMENT DIVISION), Global Clinical Development (GCD) and GCTO</li><li>
Ability to identify problems, conflicts and opportunities early and lead, analyse and prepare mitigation plans and drive conflict resolution is critical.</li><li>
Required to negotiate skillfully in tough situations with both internal and external groups; settle differences with minimum noise; win concessions without damaging relationships; be both direct and forceful as well as diplomatic; gain trust quickly from other parties in negotiations and have an excellent sense of timing. Examples of common problems include: 1) low patient recruitment, 2) inadequate staff to meet business needs, 3) performance or compliance issues, 4) working with regulatory issues and the broader organization, and 5) resolution of conflictive situations on country level.</li><li>
Requires skills to effectively build and maintain professional relationships with investigators and other external stakeholders, requiring strong communication, educational/pedagogic, diplomatic and empathic skills.</li><li><b>Experience Requirements:
</b></li></ul><p>Required:</p><ul><li>&gt;10 years of experience job experience.</li></ul><p>
Priority:</p><ul><li>People Management experience</li></ul><p>
. Saudi Market experience</p><p></p><ul><li><b>Educational Requirements:
</b></li></ul><p>Required:</p><ul><li>Bachelor degree in Science (or comparable)</li></ul><p>
Preferred:</p><ul><li>Advanced degree, (e.g., , Master degree, MD, PhD)</li></ul><p></p><p>
Current Employees apply HERE</p><p></p><p>
Current Contingent Workers apply HERE</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.</p><p></p><p><b>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p><p></p><p><b>
VISA Sponsorship:</b></p><p></p><p><b>
Travel Requirements:</b></p><p></p><p><b>
Flexible Work Arrangements:</b></p>
Not Applicable<p></p><p><b>
Shift:</b></p><p></p><p><b>
Valid Driving License:</b></p><p></p><p><b>
Hazardous Material(s):</b></p><p></p><p><b>
Required Skills:</b></p>
Adaptability, Clinical Research, Clinical Research Management, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Management Processes, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, Communication, Cross-Cultural Awareness, Decision Making, Ethical Standards, Good Clinical Practice (GCP), Leadership, Management Process, Oncology Trials, People Leadership, Production Operations, Product Operations<p></p><p><b>
 Preferred Skills:</b></p><p></p><p><b>
Job Posting End Date:</b></p>
10/13/2025<ul><li><b>A job posting is effective until 11:59:59PM on the day </b><b>BEFORE</b><b> the listed job posting end date. Please ensure you apply to a job posting no later than the day </b><b>BEFORE</b><b> the job posting end date.<br>
</b></li></ul><br>
<p><b>Requisition ID:</b>R365893</p></div>

Country Lead Associate Director Clinical Research

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)

<div></div><div><div><h5 class="jobSectionHeader"><b>Overview</b></h5>
<div></div><div><div><div>Department<b>College of Medicine</b></div>
</div><div></div><div><div>Division<b>College of Medicine</b></div>
</div></div><div></div><div><div><div>Job Family<b>Faculty- Academic
</b></div></div><div></div><div><div>Reports to<b>Vice Dean Research and Graduate Studies CoM
</b></div></div></div><div></div><div><div><div>Location<b>Alfaisal University - Riyadh
</b></div></div></div></div><div><h4 class="jobSectionHeader"><b>Job Summary</b></h4>
<p>The Postdoctoral Fellow plays a critical role in advancing translational cancer research at Alfaisal University by investigating chromatin accessibility and epigenetic reprogramming in solid tumors, integrating multi-omics datasets to identify therapeutic targets, and contributing to grant writing and interdisciplinary collaborations. This work supports the university&rsquo;s mission to develop affordable diagnostic and prognostic biomarkers for cancer and drive innovation in epigenomic and non-viral engineering. The role contributes to national healthcare priorities through research conducted in a state-of-the-art lab, supported by strategic partnerships with institutions such as KFSHRC, KAIMRC, and the Saudi FDA.</p>
<p><b>Primary Duties &amp; Responsibilities</b></p>
<ul><li>Demonstrates a research profile by producing high-quality publications in peer-reviewed journals and delivering presentations at national or international conferences to disseminate findings and enhance scientific impact.</li>
<li>Contributes actively to interdisciplinary research initiatives that align with the labs and institution&rsquo;s strategic goals, fostering collaboration across fields to address complex challenges.</li>
<li>Collaborates with academic, clinical, industrial, and governmental partners to facilitate translational and applied research that bridges fundamental science with practical applications.</li>
<li>Facilitates interdisciplinary communication by organizing seminars, workshops, or discussion forums that promote knowledge exchange and collaborative problem-solving.</li>
<li>Participates in the preparation of research proposals for external funding and supports reporting to ensure sustained project resources and compliance with grant requirements.</li>
<li>Designs, conducts, and analyzes experimental or computational research to generate valid, reproducible results across relevant scientific or engineering domains.</li>
<li>Supervisors and mentors undergraduate and graduate students to support their research development, skill acquisition, and contribution to lab goals.</li>
<li>Develops and prototypes research tools, systems, or devices, ensuring accuracy, usability, and innovation to advance experimental capabilities.</li>
<li>Builds and refines computational models or experimental systems that support data-driven investigations and contribute to knowledge advancement.</li>
<li>Contributes to the preparation and dissemination of research findings through publications, reports, and presentations to communicate effectively to scientific and professional audiences.</li>
<li>Collaborates with team members to meet project milestones, promote interdisciplinary knowledge exchange, and ensure timely progress.</li>
<li>Supports the development of software, algorithms, or analytical methods applicable to ongoing research projects to enhance data analysis and modeling capabilities.</li>
<li>Maintains research documentation and data in a professional, organized, and secure manner to ensure accuracy, reproducibility, and compliance with data management standards.</li>
<li>Performs all duties in a professional, effective, and confidential manner.</li>
<li>Performs all other related duties as required or assigned by the manager.</li>
</ul><h4 class="jobSectionHeader"><b>Qualification &amp; Experience</b></h4>
<ul><li>Doctor of Philosophy (Ph.D.) in Molecular Biology, Epigenetics, Genomics, Bioinformatics or an equivalent degree from an accredited institution.
</li><li>Minimum of three years of research experience supporting or conducting projects involving experimental, computational, or analytical work in scientific, engineering, or related fields.</li>
</ul><br>
<b>Please upload CV in ENGLISH ONLY</b></div></div><p></p>

Postdoctoral Research Fellow (Cancer Epigenetics & Omics Studies)

Explore 405+ Research in Saudi Arabia this October. Find roles across top companies and apply now to boost your career.