project coordinator

project controls manager

hr coordinator

coe & governance manager

operations coordinator

clinical study coordinator

Ray-CRO

<p>Clinical Study Coordinators are tasked with administering clinical trials. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.</p><p>KEY RESPONSIBILITIES AND TASKS</p><p>&middot; Adhere to Good Clinical Practices and the study protocols</p><p>&middot; Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials</p><p>&middot; Provide patient with written communication of their participation (i.e. copy of the signed informed consent)</p><p>&middot; Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study</p><p>&middot; Schedule all patient research visits and procedures consistent with protocol requirements</p><p>&middot; Complete and maintain case report forms, and review them against the patient&rsquo;s medical record for completeness and accuracy</p><p>&middot; Administer questionnaires/diaries/other patient material per protocol</p><p>&middot; Ensure that non-serious and serious adverse events are properly documented and reported</p><p>&middot; Manage communication with study vendors as needed</p><p>&middot; Ensure the filing and maintenance of all study documents</p><p>&middot; Schedule monitor visits and set up for monitoring visits prior to monitor&rsquo;s arrival</p><p>&middot; Act as a liaison between site staff and different departments</p><p>&middot; Saudi residency is required</p><p>. Minimum Experience 1 year .</p><p>Job Type:</p><p>Full-time</p><p>Job Type: Full-time</p>

clinical Study Coordinator

Clinical Study Coordinator

AbbVie

<div><b>Company Description</b><p><br>
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas &ndash; immunology, oncology, neuroscience, and eye care &ndash; and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.</p><b><br>
Job Description</b><p><b><br>
PRIMARY FUNCTION:
</b></p><p>Represent the affiliate&rsquo;s medical/scientific voice of expertise for assigned product(s) and relevant therapeutic area(s). Provide medical / scientific expert advice / guidance to key customers for assigned product(s) and relevant therapeutic area(s), including scientific exchange and professional relationship development with External Experts (EEs). Provide medical / scientific input into Medical Affairs strategies for the affiliate medical department and commercial plans, as required, and medical / scientific support for medical department activities under the overall direction of the Affiliate Medical Director. Provide medical affairs support to cross-functional affiliate teams. Ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.</p><p><b>
RESPONSIBILITIES:</b></p><br>
<p></p><ul><li>
Being an active brand team member to support overall strategy and execution. Provide medical/scientific input into marketing strategy and key commercial initiatives, as required.</li><li>
Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/area literature.</li><li>
Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e., pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).</li><li>
Establish and maintain professional and credible relationships with External Experts (EEs) and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums etc.</li><li>
Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.</li><li>
Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)</li><li>
Deliver training to sales forces and other departments; develop and update relevant training materials.</li><li>
Clinical Research Activities:<ul><li>
Design and implement clinical research projects within defined standards and budgets (e.g., Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).</li><li>
Provide the required oversight to manage review, approval and conduct of IIS studies.</li><li>
Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g., review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).</li></ul></li><li>
Review and preparation of promotional / non-promotional material. Ensure the medical/scientific content is correct, balanced fair and fully compliant with AbbVie&rsquo;s internal policies and guidelines and in accordance with local laws.</li><li>
Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie&rsquo;s policies and procedures and accepted standards of best practice.</li><li>
Provide input, as required, into the development of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans.</li><li>
Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.</li><li>
Operate as a scientific interface and resource to HCPs/Customer(s), Health Care Institutions, External Experts, and professional associations regarding assigned AbbVie Products or Products in Development.</li><li>
Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific data, educational initiatives, and patient safety for assigned products / therapeutic areas.</li></ul><p></p><p><b><br>
INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS:</b></p><ul><li>
In-Field/Brand Team members (as applicable)</li><li>
Affiliate R&amp;D personnel: Medical Director, Medical operation and Evidence Generation Specialist, Medical Managers/Advisors; Medical Information team / specialists; affiliate pharmacovigilance / drug safety personnel (as applicable)</li><li>
Marketing and Sales of assigned product and therapeutic area; Market access teams; Affiliate Brand teams.</li><li>
Affiliate Government Affairs; Affiliate Public Affairs; Regulatory Affairs; Legal; OEC.</li><li>
Area and HQ based Therapeutic Area medical affairs teams.</li><li>
Area Medical Affairs teams</li><li>
Medical Directors and Clinical Teams within Clinical Development Operations and Global Medical Affairs.</li><li>
Healthcare personnel (including physicians, nurses, pharmacists).</li><li>
Participating Research Investigators; thought leaders/external experts.</li><li>
Institutions and Scientific or Medical Societies.</li><li>
Hospitals, other healthcare providers, payers, and Local Regulatory Authorities.</li></ul><p><b>
LOCATION: Jeddah/Riyadh</b></p><p>
This function is hybrid in nature. Typically, up to 50% of an individual&rsquo;s time may be spent working in the field.</p><p></p><b><br>
Qualifications</b><br>
<ul><li>
Advanced degree (e.g. PharmD., PharmB., MD, PhD) in a relevant scientific discipline is preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered</li><li>
Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.</li><li><b>
Prior experience in Medical Affairs is a must with a minimum of 2 years.</b></li><li><b>
Prior experience in solid tumors and companion diagnostics CDx is a must.</b></li><li>
Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.</li><li>
Ability to comprehensively learn about new subject areas and environments.</li><li>
Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.</li><li>
An excellent understanding of written and oral English is mandatory.</li><li>
Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large.</li><li>
Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage.</li><li>
Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate&rsquo;s medical and clinical activities as necessary.</li><li>
Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.</li><li>
High customer orientation and high digital savviness skills.</li><li>
Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity</li><li>
Ability to travel regularly (approximately 50%)</li></ul><br>
<b>
Additional Information</b><div></div><p><br>
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.</p><p>
US &amp; Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><p>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p>
https://www.abbvie.com/join-us/reasonable-accommodations.html</p></div>

Medical Advisor - Oncology Solid Tumors (Based in Jeddah or Riyadh)

مجمع عيادات د/سليمان الفايز ود/محمد ابو عجمة لطب الاسنان

<p><b>HIRING in Riyadh - Transferrable Iqama only - female</b></p><p>Dental assistant , (Riyadh)</p><p>A fancy dental clinics in Riyadh - Olaya is currently offering job vacancies as <b>a dental assistant.</b></p><p><b>Job Description:-</b></p><p>&#10070;Assisting the dentist during a variety of treatment procedures</p><p>&#10070;Perform different types of dental radiographs including intra-oral, extra-oral and CBCT X-Rays</p><p>&#10070;Recording the patient's medical history</p><p>&#10070;Triaging the dental patients including blood pressure and pulse</p><p>&#10070;Preparing dental instruments for sterilization</p><p>&#10070;Implement environmental surfaces infection control measures as per policies in force</p><p>&#10070;Helping patients feel comfortable before, during and after dental treatment</p><p>&#10070;providing patients with instructions for oral care following surgery or other dental treatment procedures based on the dentist instructions</p><p>&#10070;Taking impressions and optical impressions of patients' teeth for study casts (models of teeth)</p><p>&#10070;Performing office management tasks that often require the use of a personal computer</p><p>&#10070;Communicating with patients and dental coordinators (e.g., scheduling appointments, answering the telephone, billing and ordering supplies)</p><p>&#10070;Helping to provide direct patient care in all dental specialties, including orthodontics, pediatric dentistry, periodontics and oral surgery</p><p>&#10070;Escorting the patient from and to the waiting area, to the cashier office after treatment</p><p>&#10070;Assist dentist in management of medical or dental emergencies</p><p>&#10070;Maintain an updated SCHS license, BLS and other required licenses as per local regulation in force</p><p>&#10070;Implement dental department policies and procedures</p><p>&#10070;Submit replenishment requests to the dental coordinator</p><p>&#10070;Maintain the dental clinic inventory of materials, disposables and equipment; and ensure reporting any issues or discrepancies through the assigned channels</p><p>&#10070;Monitor and report expired dental materials</p><p>&#10070;Maintain an up to date dental laboratory cases records and update the dentist on the same</p><p>&#10070;Maintain patients&rsquo; confidentiality.</p><p><b>QUALIFICATIONS:-</b></p><p>- Three <b>year</b> of related experience with Bachelor's or <b>five</b> year (and up) years with<br/>Associate Degree/Diploma is required.</p><p>- Must have a professional classification certificate (SCFHS)</p><p>- <b>Transferrable Iqama</b></p><p><b>Benefits :-</b></p><p>- Free accommodation</p><p>- Free transportation</p><p>- Friendly environment</p><p>- Salary range starting from 5000SR based on the certificate and experiences.</p><p><b>Contact Information:-</b></p><p>Email/ alfayez.abuajmah@gmail.com</p><p>whasapp : 00966582754814</p><p>Job Types: Full-time, Contract</p><p>Pay: &#65020;4,500.00 - &#65020;6,000.00 per month</p>

Dental assistant

Diaverum

<div></div><div><div><div><div><div><p>Clinical Pharmacist - 9008 - Riyadh - &#1575;&#1604;&#1585;&#1610;&#1575;&#1590;
</p></div></div></div></div><div><div><div><div><b>Location:
</b>Riyadh, SA, 7929
</div></div></div></div><div><div><div><div><b>Date Posted: </b>27 Aug 2025
</div></div></div></div><div><div><div><div><b>Contract type: </b>Permanent
</div></div></div></div><div><div><div><div><b>Work Type: </b>On-site
</div></div></div></div><div><div><div><div><b>Part Time / Full Time: </b>Full Time
</div></div></div></div><div><div><div><div><div><b>About Diaverum:</b></div>
<div>
We are a purpose-driven organization &ndash; delivering life-enhancing renal care because everyone deserves a fulfilling life. Our standardized, world-class care delivery sets us apart. Diaverum provides life enhancing renal care to patients with Chronic Kidney Disease (CKD), enabling them to live fulfilling lives. We are one of the world&rsquo;s leading providers of renal care and the largest service provider in the Middle East. Our core service is hemodialysis, but our expertise stretches far beyond this. We offer support and treatments ranging from preventive care, peritoneal dialysis and home care to the coordinated management of patients&rsquo; comorbidities and transplant services. At the heart of what we do is our highly standardized proprietary care delivery model, supported by a continuously evolving digital infrastructure.</div>
<div>
For more details, please visit our website &ndash;<b> </b>Diaverum Saudi Arabia</div><div><br>
<b>
About the Role:</b></div>
<div>
To be responsible for the pharmaceutical care management for assigned clinic(s) by ensuring excellence in service delivery according to Diaverum clinical governance five core practices (clinical standards, medical standards, performance measurement, education, and scientific research). To plan, coordinate, deliver, and evaluate the pharmaceutical care service , be responsible provision of drug therapy for purpose of achieving definite therapeutic outcome that improve the patient quality of life ), wellbeing and health promotion (educational activities), Pharmaceutical supply management, scientific research and preventive care services to provide Life Enhancing Renal Care</div><br>
<div></div>
<div><b>
Key Responsibilities:</b></div>
<div><b>
DEFINITION OF REPORTING LINES</b></div>
<ul>
<li><div>Pharmacist is accountable towards the Direct Manager with regards to meeting clinic objectives including administrative, business, medical and operational outcomes.</div>
</li>
<li><div>Pharmacist is accountable towards the Function Head with regards to ensuring standards of care and quality management, further specified below.</div>
</li>
<li><div>Annual performance evaluation, including training and development needs, is a shared responsibility between the Direct Manager and Function Head towards the Pharmacist.</div>
</li>
</ul><div><b>ROLE WITHIN THE MULTIDISCIPLINARY TEAM (MDT)</b></div>
<ul>
<li><div>Aim to cultivate pharmaceutical care that is patient-centric, evidence-based and integrated within Diaverum care delivery system.</div>
</li>
<li><div>Work in collaboration with the MDT and patients to support patients to navigate their disease, disease complications, dialysis treatment and required medication / lifestyle changes.</div>
</li>
<li><div>Initiate and take lead in managing pharmaceutical and preventive care projects in coordination and alignment with Head of Pharmaceutical Care and other strategic departmental and organizational projects as appropriate.</div>
</li>
<li><div>Point of contact in the clinic for medical, nursing, operations and other functions with all matters concerning the pharmaceutical care of patients.</div>
</li>
</ul><div><b>PHARMASUTICAL /MEDICAL/CLINICAL PERFORMANCE</b></div>
<ul>
<li><div>Ensure effective drug therapy, health promotion, and lifestyle management supporting patients with different demographic background (gender, age, educational level), medical history and psychosocial status.</div>
</li>
<li><div>Ensure implementation of a continuous, accurate and effective pharmacotherapy plan for all patients. includes screening, assessment, diagnosis, intervention/reconciliation, documentation, monitoring, and evaluation.</div>
</li>
<li><div>Manage the set clinical parameters to accurately measure, monitor and evaluate all aspects of pharmaceutical care in accordance to national and international standards and guidelines in renal care and chronic disease management.</div>
</li>
<li><div>Utilize clinical knowledge and counselling skills to make a positive difference in patients&rsquo; quality of life.</div>
</li>
<li><div>Utilize clinical knowledge and counselling skills to make a positive difference in patients&rsquo; medical management.</div>
</li>
<li><div>Engage and actively participate in dietetic research led by the pharmaceutical care department.</div>
</li>
</ul><div><b>PHARMASUTICAL SUPPLIES:</b></div>
<ul>
<li><div>Manage Pharmaceutical Supplies with ensure both (Medications Safety/ Product Quality (in terms of shipping, delivery, storage and preparation), availability of the product to cover any situation of need.</div>
</li>
</ul><ul><li><div>Coordinate with Logistics Services regarding quality &amp; availability, submit accurate reports to determine the need continuously - submit accurate reports of critical pharmaceutical items ahead of time to SC.</div>
</li>
<li><div>Review all pharmaceutical stock data that like: slow moving item, over stock items, nearly expired items and zero stock items &hellip; etc. and give recommendations.</div>
</li>
<li><div>Study the drugs statistical reports to develop appropriate solutions for any deficit.</div>
</li>
<li><div>Ensure following medication manufacturing recommendations in all medications management steps.</div>
</li>
<li><div>Make necessary consumption analysis to improve clinic consumption take patients need into consecration at all times.</div>
</li>
<li><div>Coordinate with MDT / Logistics Services team to prevent the waste of pharmaceutical supplies.</div>
</li>
<li><div>Stay abreast of the latest updates in the pharmaceutical industry to obtain the best quality products as the available capabilities allow.</div>
</li>
<li><div>Follow all pharmaceutical supplies P&amp;P accordingly.</div>
</li>
</ul><div><b>POLICIES AND PROCEDURES</b></div>
<ul>
<li><div>Understand and comply with policies and procedures related to scope of care, patient confidentiality/ rights, infection control, facility management and safety, as well adhering to time/attendance and dress code requirements.</div>
</li>
<li><div>Understand policies and procedures and apply them to meet patient&rsquo;s need as determined by the medical staff prescription order.</div>
</li>
<li><div>Adhere to current policies and procedures and future updates in Diaverum including quality standards such as Joint Commission International (JCI) and/or Saudi Central Board for Accreditation of Healthcare Institutions (CBAHI), medical KPIs as well as all local regulatory requirements governing nutrition care.</div>
</li>
<li><div>Monitor compliance according to all pharmaceutical care policies and procedures and country regulations.</div>
</li>
</ul><div><b>QUALITY MANAGEMENT</b></div>
<ul>
<li><div>Work closely with Head of Pharmaceutical Care, Clinic Medical Director, Clinic Team, and Operation managements in achieving overall quality goals and medical parameters.</div>
</li>
<li><div>Participate in Pharmaceutical care department meetings, clinic management meetings including quarterly management review (QMR) and monthly business review meetings (MBR).</div>
</li>
<li><div>Participate in country and clinic development initiatives (projects) while ensuring alignment with Diaverum Pharmaceutical care department strategy and vision.</div>
</li>
</ul><div><b>PHARMACIST LEARNING AND DEVELOPMENT</b></div>
<ul>
<li><div>Participate and engage in all provided training programs and continuous professional development of pharmaceutical care.</div>
</li>
<li><div>Participate in the orientation and induction of new members of pharmaceutical team as applicable.</div>
</li>
<li><div>Participate in self and other&rsquo;s education, training and development including assigned pharmacist interns as applicable.</div></li></ul><br>
<div>
</div><div><b>QUALIFICATIONS</b></div>
<div><b>
EDUCATION</b></div>
<ul>
<li><div>Bachelor&rsquo;s degree in Doctor of Pharmacy</div>
</li>
<li><div>Certified Pharmacist Specialist by the Saudi Commission for Health Specialties (SCFHS)</div>
</li>
</ul><div><b>EXPERIENCE</b></div>
<ul>
<li><div>Fresh Graduate, 1-2 years clinical dietetics experience in a clinical setting or hospital is favorable.</div>
</li>
<li><div>Experience in clinical specialty favorable (renal, diabetes, hypertension)</div>
</li>
</ul><div><b>LANGUAGES</b></div>
<ul>
<li><div>Fluent in Arabic and English (spoken and written)</div>
</li>
</ul><div><b>IT SKILLS</b></div>
<ul>
<li><div>Computer operating experience and MS Office skills are required.</div></li></ul><br>
<div>
</div><div>This is a great opportunity to join a purpose-driven and growing healthcare organization that values competence, inspiration, and passion.</div>
<div>
Join a global team where your contribution matters &mdash; and where every role supports the delivery of life-enhancing renal care.</div></div></div></div></div></div><p></p>

Clinical Pharmacist - 9008 - Riyadh

<div><p>WSP is looking for Principal Engineer &ndash; Power System Studies with over 10-15 years&rsquo; experience of providing technical leadership to deliver the projects while meeting the contract requirements with respect to quality, time and budget. The incumbent will be providing overall technical leadership to the WSP clients in the region and will be acting as the single point of contact for all the middle east clients while also being involved in the business development activities.</p></div>
<br><div><p><b>The key objectives of the roles are to:
</b></p><ul><li>Power system analysis of transmission and distribution projects.
</li><li>Feasibility studies, masterplans, despatch studies, renewable integration, grid code reviews
</li><li>Preparation of Renewable generation connection schemes from distribution to utility scale generation including determining techno-economical optimum amount of renewable generation.
</li><li>Load flow study, fault level calculations, harmonic analysis, voltage stability and transient stability analysis on transmission, distribution, and industrial power systems, using DIgSILENT, PSS/E, PLEXOS, ETAP, CYME PSAF, ASPEN OneLiner, ASPEN database and IPSA+.
</li><li>Review all the Power System Studies technical submittals by EPC contractor / Developers in reference to Client&rsquo;s Electricity Transmission Code and International standards as applicable.
</li><li>Review the Power system models developed by EPC contractor specific to each study.
</li><li>Attend all the required meetings &amp; address all the technical clarifications raised by EPC contractor / Developer.
</li><li>Attend the FAT &amp; SAT visits to ensure all the performance criteria are met related to grid compliance requirements. The test shall be conducted with RTDS or other similar tools.
</li><li>Review the updated model received from EPC based on FAT/SAT reports and ensure all the grid compliance requirements are met as agreed during the detail design stage.
</li><li>Assist Client to incorporate equipment models provided by EPC contractor into the TRANSCO network PSSE &amp; PSCAD models suitable for various planning studies (steady state and dynamics).
</li><li>The power system studies review work shall briefly include, but not limited to the following:
<ul><li>Reactive power capability study
</li><li>Grid impact study
</li><li>Transient and dynamic stability studies
</li><li>Insulation co-ordination study
</li><li>Switching transient study
</li><li>Faulted transient switching study
</li><li>Transformer Energization study
</li><li>AC/DC harmonics and flicker study
</li><li>AC/DC harmonic filter sizing report
</li><li>Harmonic impedance locus identification and analysis study
</li><li>AC protection relay setting coordination study
</li><li>Sub-synchronous resonance studies
</li><li>All required ETC compliance studies</li></ul></li></ul></div><p></p>
<br><div><p><b>We'd love to hear from you if you have:
</b></p><ul><li>Master&rsquo;s Degree in Electrical / Power systems Engineering.
</li><li>Minimum 10-15 years of working experience with similar capacity.
</li><li>Proficient with Power system study softwares like PSS Sincal, PSSE, PLS CAD, Dig silent etc.
</li><li>Must have experience in Power System Studies, Grid Impact studies, on Transmission and Distribution projects etc.
</li><li>Having indepth knowledge of software languages (Python/Java) to automate the processes will be an added advantage.
</li><li>Incumbent is expected to have prior experience of working with electrical utilities like TRANSCO/SEC/ADDC having successfully delivered Power System Studies related projects.
</li>People managing skill, with excellent written and verbal skills. Able to build excellent client relations through communication and multidisciplinary coordination skills<br>
<li>
</li></ul><p></p><p><b>Imagine a better future for you and a better future for us all.
 </b></p><p>Join our close-knit community of talented individuals who share your passion for making a positive impact. Our global team includes more than 69,000 employees, working together to make a difference in communities both close to home and around the world.
 </p><p><b>With us, you can. Apply today.<br>
</b></p><p></p><p><b>LI#Onsite</b></p></div><br><div></div>

Principal Engineer - Power Systems

KEO International Consultants

<div>Overview:
<div>
KEO is a creative enterprise, where innovation is a way of life. We are uniquely resourced with end-to-end services to take clients from inspiration &ndash; through conceptualization &ndash; to realization of planning, design or project delivery in the built and natural environments. For over 60 years we&rsquo;ve led with vision, contributing to many of the world&rsquo;s most ambitious projects, iconic places, remarkable experiences and prosperous communities.</div><div>
As a highly integrated and agile AEP/PMCM firm, KEO is recognized by ENR as one of the Top 225 International Design Firms and one of the Top 20 International PM/CM Firms. We are also ranked by World Architecture as the 57th largest global architecture firm and the #1 Firm in the Middle East Region in their 2024 WA100 Survey.</div><div>
We invite you to join us. Why?</div><div>
When you join KEO, you&rsquo;ll discover more than just a job &ndash; you&rsquo;ll find a supportive environment that fosters your professional development through internal global mobility and career development and does so within a culture that supports company-wide health and well-being through on-demand counselling services and regular workplace clinics. You will be invited to celebrate community events such as sports days, fun-runs, in-house sports teams and beach clean ups. In addition to your competitive package and benefits you will have access to a suite of policies that include hybrid working arrangements, individual athletic sponsorship, study assistance sponsorship, employee referral rewards, mentoring and coaching programs and extensive in-house on demand learning courses.</div><br>
<div></div>
Responsibilities:
<div>
Our newest opportunity is for a talented <b>BIM Coordinator/ Engineer</b> to join our team based in Riyadh, Saudi Arabia.</div><div></div><p><br>
We envisage success in this role to include;</p><ul><li>
Preparing, review 3D models (Arch/Str) for all the assets in the projects (buildings, roads, gates&hellip;etc.).</li><li>
Preparing and reviewing Primavera P6 schedules.</li><li>
Creating 4D models, monthly 4D progress reports, Animation.</li><li>
Designing 3D logistics plans.</li><li>
Preparing and delivering presentations to client management teams.</li><li>
Aligning models breakdown with the program WBS and vice versa.</li><li>
Coordinating 4D information between planning, construction, and technical teams.</li><li>
Managing and coordinating BIM standards development, implementation, and quality on all related files and models.</li><li>
Developing and implement project 4D strategy and understand the scope of work for all stockholders.</li><li>
Troubleshooting any BIM related issues</li><li>
Attending &amp; calling for coordination Meetings</li></ul>
Qualifications:
<div>
To be successful in this dynamic opportunity, we envision that you will bring a minimum of 6 years of experience partnered with Bachelor's Degree in Architecture or equivalent field.</div><div></div><div><br>
Advanced proficiency in a range of computer aided design tools including Autodesk Revit, Navisworks and various Revit add-ins such as Dynamo, and integration tools with Specification, Energy Analysis, Cost control, Engineering analysis.</div><div></div><div><br>
Advance proficiency in BIM360 Docs and Design (ACC).</div><div></div><div><br>
KEO&rsquo;s performance is founded upon integrity, results, innovation, safety and our people. We embrace diversity and recognise its&rsquo; contribution to client success wherever we work.</div><div></div><div><br>
We are excited to hear how you can partner with our award-winning team and treat all expressions of interest confidentially.</div></div>

BIM Coordinator/ Engineer

Explore 262+ Clinical study coordinator in Ksa this September. Find roles across top companies and apply now to boost your career.