senior project manager

hr specialist

procurement specialist

accounting specialist

compliance specialist

senior regulatory affairs specialist

SERVIER

<div></div><div><div><div><div><div><b>Date posted: </b>Sep 10, 2025
</div></div></div></div><div><div><div><div><b>City: </b>Riyadh
</div></div></div></div><div><div><div><div><b>Country/Region: </b>SA
</div></div></div></div><div><div><div><div><b>Type of Contract: </b>Full-time Employment / Unlimited
</div></div></div></div><div><div><div><div><b>Job Requisition ID: </b>9758
</div></div></div></div><div></div><div><div><div><div><p>Regulatory Affairs Specialist - KSA
</p></div></div></div></div><div><div><div><div><div>.</div>
<p><b>
Job Purpose</b></p>
<ul>
<li>The Regulatory Affairs Specialist focuses on ensuring that the organization meets all of the applicable regulations. Their goal is to ensure that new products meet certain requirements as set by Health Authorities.</li>
<li>Regulatory Affairs Specialist ME is responsible for Saudi Arabia activities (KSA).</li>
<li>Identifying all elements and actions necessary for registering and maintaining valid marketing authorizations in KSA.</li>
<li>Collaboration with the local partners, local authorities and WRA in France.</li>
<li>Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals or registrations.</li>
<li>Handle registrations of new products/sites/medical devices, pricing as well as maintaining life cycle of products in KSA, including renewals and variations.</li>
<li>Ensure that all relevant regulations are fully met in dossiers, with the aim of complying with the requirements established by Health Authorities.</li>
<li>Collaborates closely with the Department Head in all department related tasks and activities.</li>
<li>Compile and prepare new products and manufacturing sites registration files for submissions to authorities in KSA as per Regulatory timelines.</li>
<li>Cross functionality &amp; collaboration with Global teams as well as all ME departments, provide regulatory support and guidance whenever required.</li></ul><br>
<p></p>
<p><b>
Role Responsibilities</b></p>
<p><b>
Life-Cycle </b><b>management of products</b></p>
<ul>
<li>Pre-registration coordination with WRA and preparation of documentation for KSA to compile the product and manufacturing site files, Review/ Preparation/Submission of dossiers, fees, inquiries, answers to questions, approvals...</li>
<li>Life-cycle management of products that includes new registrations, renewals/minor variation of both products and sites.</li>
<li>Follow country specific procedures and SFDA guidelines in the KSA market.</li>
<li>Coordination &amp; liaising with WRA teams/distributors for preparation of all types of regulatory dossiers &amp; local documentation.</li>
<li>Preparation of price forms and related documentation for new product registration files.</li>
<li>Liaising with WRA, agents and authorities for documentation submission and follow-up and keep track.</li>
<li>To keep track of the registration status of products with submission, registration, expiry dates.</li>
</ul>
<p><b>Regulatory Tasks</b></p>
<ul>
<li>Closely collaborate with the Head of the Department for all regulatory tasks.</li>
<li>Monthly Reports, Correspondences/Mails, Scientific Office Renewal at the SFDA.</li>
<li>Involved actively in the budget preparation of KSA Regulatory Affairs.</li>
<li>Follow-up on regulatory guidelines and ensure sharing of regulatory information with all concerned.</li>
<li>Reference standard submissions to the authorities.</li>
<li>Helping the Supply Chain Department for tenders - preparation of documentation for institutional tender submissions.</li>
<li>Actively involved in Regulatory Audits.</li></ul><br>
<p></p>
<p><b>
Regulatory Site Management
</b></p><ul><li>For all activities related to KSA -WRA Portal, Ereca, Solaris, LSRIMS, Cosac.</li>
</ul>
<p><b>Other related tasks</b></p>
<ul>
<li>Management/Organizing department supported conferences for Health Authorities in the ME countries.</li>
<li>Liaise closely with agent and Health Authorities in KSA.</li>
<li>Responsible for Change Controls for Variations for the ME region.</li>
<li>Work as a deputy for the local responsible person for advertisement/promotional material.</li>
<li>Deputy Local Responsible person for validation of Packaging Items.</li>
<li>Cross collaboration with other ME departments.</li></ul><br>
<p></p>
<p><b>
Dimensions</b></p>
<ul>
<li>Geographical span: ME - KSA.</li>
<li>Work with the ME Regulatory Lead to develop a detailed understanding of regulatory guidelines and technical requirements in KSA.</li>
<li>Life cycle management of products, understanding of industry-specific regulations, audit procedures, and the ability to ensure compliance with regulatory standards.</li>
<li>Work and support the KSA Regulatory Affairs team.</li>
<li>Cross-functionality with other departments.</li>
<li>Report to the Head of the Department.</li></ul><br>
<p></p>
<p><b>
Requirements</b></p>
<p><b>
Educational</b><b> </b><b>qualifications</b></p>
<ul>
<li>Bachelor&rsquo;s Degree in Pharmacy / Science.</li>
</ul>
<p><b>Relevant Experience</b></p>
<ul>
<li>3+ years of relevant pharmaceutical regulatory experience within a large multinational organization.</li>
<li>Experience working in Saudi Arabia (preferred).</li>
<li>Experience of working within a Global pharmaceutical company would be an advantage.</li></ul><br>
<p></p>
<p><b>
Skills &amp; Personal characteristics</b></p>
<ul>
<li>Good knowledge of the Regulatory environment and procedures in KSA.</li>
<li>Sharp Regulatory Intelligence.</li>
<li>Ability to work cross functional to resolve complex issues.</li>
<li>Strategic thinker, innovative, able to drive multiple-simultaneous initiatives, able to work under pressure, team player.</li>
<li>Multi-tasking, organized, Process &amp; Result oriented, Focused, Problem solving, good judgment and decision-making capability.</li>
<li>Excellent interpersonal, Negotiation and relationship building skills.</li>
<li>Excellent interpersonal, communication &amp; digital skills.</li>
<li>Written and spoken fluency in English &amp; Arabic (French is an added advantage).</li></ul><br>
<div></div>
<div>Whatever your area of expertise, your work within the Servier Group helps advance therapeutic progress for the benefit of patients. You will be part of teams recognized for their scientific excellence and reach your full potential in a professional environment that encourages you to develop yourself. Tailor-made onboarding journeys, mobility opportunities, quality trainings, responsible management, team spirit... All this and more in a workplace focused on your well-being.</div><br>
<div></div>
<div>At Servier, we are committed to therapeutic progress to serve patient needs. We put the diversity of our employees as a source of richness for the fulfillment of this vocation.</div></div></div></div></div></div><p></p>

Regulatory Affairs Specialist - KSA

Zahrawi Medical

<p></p><div><div><div><div><div><h6 class="jobSectionHeader"><b>About Zahrawi Group</b></h6>
<p>Zahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE, KSA, Qatar, Bahrain, &amp; Oman markets. The company supplies and distributes high-quality products and services to Hospitals, Clinics, Laboratories, &amp; Analytical Industries.
</p></div><div><h6 class="jobSectionHeader"><b>job Brief</b></h6>
The incumbent is responsible for all Product Classification/Manufacturing Site Registration and Product Registration and to ensure that all documents required are available and are submitted on time.
</div><div><div><p>They are also responsible for the preparation of the pre- and final permits for the imported items as per the SFDA guidelines.</p><p><b>
ACCOUNTABILITIES</b></p><p><b>
Policies &amp; Procedures:</b></p><ul><li>
Adhere to all Zahrawi Policies &amp; Procedures as applicable.</li></ul><p><b>
Regulatory Affairs:</b></p><ul><li>
Ensure that Zahrawi&rsquo;s products comply with the regulations of the SFDA.</li><li>
Keep up to date with the latest changes in regulatory legislation and guidelines.</li><li>
Liaise and negotiate with regulatory authority to ensure a smooth registration process.</li><li>
Provide advice about regulations to customers/suppliers.</li><li>
Analyze product complaints and make recommendations to solve the problem and to avoid them in the future.</li></ul><p><b>
Product Classification &amp; Registration:</b></p><ul><li>
Ensure that all required documents and actions for Product Classification/Manufacturing Site Registration and Product Registration are available.</li><li>
Prepare all required documents to be submitted for Product Classification under SFDA.</li><li>
Prepare all required documents to be submitted for Manufacturing Site registration under SFDA.</li><li>
Prepare all the Dossiers to be submitted to SFDA for medical, pharmaceuticals and GSL products.</li><li>
Prepare and submit samples to SFDA for product registration completion.</li><li>
Collect all necessary documents from Supplier to submit for SFDA of products under Ghad System.</li><li>
Register reagents with restricted elements through Ghad System.</li></ul><p><b>
Importation Permits:</b></p><ul><li>
Prepare and apply for the pre-permit document as per the SFDA guidelines and verify the items being imported and the documents required.</li><li>
Apply for the MOH Narcotics and Pre-cursor Chemical permits on the SFDA website as per the specified guidelines.</li><li>
Register and submit the permits through Ghad system.</li><li>
Resubmit any permits that have not been approved and make sure all the information provided is correct and attach any new documents if required.</li><li>
Prepare weekly / monthly report regarding the rejections/ delays for SFDA importation permits and reasons related to that.</li><li>
Check and review the safety data sheet of the restricted element to prepare the required documents for obtaining MOI approval.</li></ul><p><b>
Exportation Permits:</b></p><ul><li>
Prepare the required documents necessary for obtaining SFDA approval to export medical products outside KSA.</li></ul><p><b>
Importation Rules &amp; Regulations:</b></p><ul><li>
Communicate with the existing and new suppliers regarding SFDA importation rules and policies.</li><li>
Upload on the SFDA importation system any new classifications or registration certificates.</li><li>
Ensure that all urgent request from the Sales team and suppliers are dealt with in a fast manner and ensure that all documents are in place.</li><li>
Report any deviation from SFDA guidelines of imported shipments and take the corrective and preventive action accordingly.</li><li>
Review on a regular basis the SFDA importation process of distribution agreements.</li><li>
Ensure that the SFDA license is renewed before expiry date to avoid importation disturbance.</li><li>
Segregate the imported products as per HS code in coordination with logistic team and confirm if products are SFDA regulated or not.</li><li>
Coordinate with the Procurement &amp; Logistics Team to update all the required documents in time to avoid importation rejections.</li></ul><p><b>
Audit:</b></p><ul><li>
Prepare any documentation needed for internal and external audits.</li><li>
File all documents in the corresponding files to ensure all are available and are correct.</li><li>
Evaluate the suggestions after the audit and implement them when possible.</li></ul><p><b>
Admin:</b></p><ul><li>
Assist the Warehouse Coordinators with relevant documents when requested.</li><li>
Coordinate with the Procurement team and assist them with any question they or the Suppliers may have related to SFDA importation.</li></ul><p><b>
Note: Zahrawi employees must step into other work assigned to them as business needs arise and are not limited to the above.</b></p><p><b>
REQUIREMENTS</b></p><ul><li><p><b>
Education:</b> Bachelor&rsquo;s degree (Biology/ Pharmacy/ Biomedical or Science related major is an advantage)</p></li><li><p><b>
Experience:</b> 2-3 years of relevant experience in regulatory affairs</p></li><li><b>
Job Specific Skills:</b> Effective Communication skills &amp; Good English - Time management skills - Problem Solving Skills - Good computer skills in Ms. Office (Excel&ndash; ERP/Oracle system) &ndash; Process Management skills &ndash; Detail Oriented &ndash; Knowledge about Saber System &amp; Ghad System - Knowledge in SFDA regulations.</li><li><p><b>
Additional Details:</b> Candidate should be Saudi National and based in Riyadh, KSA.</p></li></ul>
</div></div><p></p><p>Location: KSA - Riyadh
</p><p></p><p>Job Type: FULLTIME
</p><p></p><p>Job Posting Date: 03-09-2025
</p><p>Division/Department: Regulatory Affairs and Pharmacovigilance</p></div></div></div></div><p></p>

Regulatory Affairs Executive/Specialist

Parsons

<div><p>In a world of possibilities, pursue one with endless opportunities. Imagine Next!
</p><p></p><p>When it comes to what you want in your career, if you can imagine it, you can do it at Parsons. Imagine a career working with intelligent, diverse people sharing a common quest. Imagine a workplace where you can be yourself. Where you can thrive. Where you can find your next, right now. We&rsquo;ve got what you&rsquo;re looking for.
</p><p></p><p><b>Job Description:
</b></p><p>Parsons is looking for an amazingly talented <b>Senior Document Controller Permits </b>to join our team! In this role you will get to oversee the management, control, and safekeeping of all permits, NOCs, and related documentation within the Permitting Office.
</p><p></p><p><b>What You'll Be Doing:
</b></p><p></p><p><b>What Required Skills You'll Bring:
</b></p><ul><li>Bachelor&rsquo;s degree in Business Administration, Records Management, or related field.
</li><li>5+ years of document control experience, ideally in permitting or large-scale projects.
</li><li>Strong knowledge of document management systems.
</li><li>High attention to detail and strong organizational skills.
</li><li>Proficiency in English; Arabic preferred.
</li></ul><p></p>Parsons equally employs representation at all job levels no matter the race, color, religion, sex (including pregnancy), national origin, age, disability or genetic information.
<p></p><p>We truly invest and care about our employee&rsquo;s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest&mdash;APPLY TODAY!
</p><p></p><p>Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/ .</p></div>

Senior Document Controller Permits (Saudi National)

<div><p>Our globally coordinated tax professionals offer connected services across all tax disciplines to help our clients thrive in an era of rapid change. We combine our exceptional knowledge and experience with the people and technology platforms that make us an ideal partner for all their tax-related needs. In Tax, we equip clients to make better business decisions by bringing insights to the forefront. We help companies understand the tax policies and tax laws of governments around the world to plan and comply accordingly.</p><p></p><p><br>
Our teams leverage transformative technologies to deliver strategy and execution, from tax and regulatory obligations to operations and workforce management, to reduce risk and drive sustainable value. Tax has six sub-service lines which cover a wide range of issues: Business Tax Services, Global Compliance and Reporting, Global Law, Indirect Tax, International Tax and Transaction Services and People Advisory Services.</p><p></p><p><b><br>
The opportunity</b></p><p></p><p><br>
Our ACR tax service line operates as a team of highly experienced tax professionals who focus on delivering efficient and effective resources to companies in the region. Our goal is to improve quality, manage risk, create efficiency and drive value. Our market leading approach combines standard and efficient processes, highly effective tools and an extensive network of local tax and accounting professionals.</p><p></p><p><br>
You will have the opportunity to provide clients an integrated, consistent, quality service that unlocks the potential of the compliance function, with tax compliance, statutory accounts preparation and tax accounting calculation support.</p><p></p><p><b><br>
Your key responsibilities</b></p><p></p><p><br>
 You will be assisting clients in their financial digital processes (e.g. preparation and interpretation of year-end-closings, audit assistance, financial statements, etc.), tax compliance (corporate tax returns and VAT returns, etc.), general accounting, credit control and internal optimization projects. You will also be responsible for management reports, budgeting, analytical bookkeeping, financial health and competitors&rsquo; analysis.</p><p></p><p><br>
You will be responsible for overall day to day requirements in client engagements, monitor progress and deliverables, put in place the necessary standardized processes, anticipate and identify risks, resolve or escalate issues as appropriate and drive performance-improvement solutions.</p><p></p><p><br>
You will also be responsible for ensuring adherence to our Tax Quality guidelines.</p><p></p><p><b><br>
Skills and attributes for success</b></p><p></p><p><br>
If you are an excellent communicator and detail oriented professional with a strong track record of management experience who is comfortable working across borders with a wide network of people and with large amount of data, you will be perfect for the role.</p><p></p><p><b><br>
To qualify for the role you must have</b></p><br>
<p></p><ul><li>
A bachelor's degree with strong academic credentials in accounting, business, finance, taxation or any related essential fields.</li><li>
Professional qualifications e.g. CA, CPA, ACCA, CTA, ADIT or equivalent qualification is a must.</li><li>
Minimum 3 years of relevant experience, ideally within a large professional services company or similar environment.</li><li>
Extensive and in-depth knowledge of Financial Reporting Standards, relevant tax rules, procedures and guidelines.</li><li>
Excellent Command of spoken and written English. Arabic will be an advantage.</li></ul><p></p><p><b><br>
Ideally, you also have</b></p><br>
<p></p><ul><li>
Experience of dealing with multinational clients and ability to work in multi-cultural environment.</li><li>
Experience and knowledge of tax compliance, financial reporting and ERP systems such as SAP.</li><li>
Demonstrated good understanding and capability of implementing accounting concepts.</li><li>
Excellent analytical skills.</li><li>
Effective organization and time management skills with ability to work under pressure and adhere to project deadlines.</li><li>
Ability to multitask and work efficiently in a fast-paced environment</li></ul><p></p><p><b><br>
What we look for</b></p><p></p><p><br>
Highly motivated individuals with excellent problem-solving skills and the ability to prioritize shifting workloads in a rapidly changing industry. An effective communicator, you&rsquo;ll be a confident team player that collaborates with people from various teams while looking to develop your career in a dynamic organization.</p><p></p><p><b><br>
What we offer</b></p><p><br>
We offer a competitive compensation package where you&rsquo;ll be rewarded based on performance and recognized for the value you bring to our business. Plus, we offer:</p><ul><li>
Continuous learning: You&rsquo;ll develop the mindset and skills to navigate whatever comes next.</li><li>
Success as defined by you: We&rsquo;ll provide the tools and flexibility, so you can make a meaningful impact, your way.</li><li>
Transformative leadership: We&rsquo;ll give you the insights, coaching and confidence to be the leader the world needs.</li><li>
Diverse and inclusive culture: You&rsquo;ll be embraced for who you are and empowered to use your voice to help others find theirs.</li></ul><p></p><p><b><br>
If you can demonstrate that you meet the criteria above, please contact us as soon as possible.</b></p><p><b><br>
The exceptional EY experience. It&rsquo;s yours to build.</b></p><p><b><br>
EY | Building a better working world</b></p><p></p><p><br>
EY exists to build a better working world, helping to create long-term value for clients, people and society and build trust in the capital markets.</p><p></p><p><br>
Enabled by data and technology, diverse EY teams in over 150 countries provide trust through assurance and help clients grow, transform and operate.</p><p></p><p><br>
Working across assurance, consulting, law, strategy, tax and transactions, EY teams ask better questions to find new answers for the complex issues facing our world today.</p></div><p></p>

Senior - Compliance & Reporting - Jeddah & Riyadh

Safwat Al-Khaleej

<p><b>Company: </b>A Leading Healthcare Provider in Riyadh<br/><b>Location:</b> Riyadh, Saudi Arabia<br/><b>Job Type:</b> Full-time, Senior Leadership</p><p><b>About Us</b></p><p>Client is a premier, state-of-the-art medical facility in the heart of Riyadh, renowned for its exceptional patient care, cutting-edge technology, and world-class medical expertise. We are committed to advancing healthcare in the Kingdom of Saudi Arabia through innovation, research, and the highest standards of clinical excellence. As we continue to grow and shape the future of healthcare, we are seeking a visionary and strategic leader to join our executive team as the Director of Medical Affairs.</p><p><b>The Opportunity</b></p><p>This is a unique opportunity to play a pivotal role at the intersection of clinical medicine, administration, and strategic leadership. As the Director of Medical Affairs, you will be the key link between our medical staff and executive management, ensuring the delivery of superior patient care while driving medical governance, quality improvement, and clinical research initiatives. Your work will directly impact our reputation, our patients' outcomes, and the professional development of our medical staff.</p><p><b>Key Responsibilities:</b></p><p><b>Strategic Leadership &amp; Governance:</b></p><ul><li>Develop and execute the medical affairs strategy in alignment with the hospital's overall mission and vision.</li><li>Chair and provide secretariat support to key medical committees (e.g., Medical Advisory, Credentials, Ethics).</li><li>Oversee the implementation and adherence to hospital medical bylaws, rules, and regulations, ensuring compliance with Saudi Council for Health Specialties (SCFHS) and Saudi Central Board for Accreditation of Healthcare Institutions (CBAHI) standards.</li><li>Manage the medical staff credentialing, privileging, and re-appointment processes.</li></ul><p><b>Quality &amp; Patient Safety:</b></p><ul><li>Lead hospital-wide quality improvement and patient safety programs in collaboration with the Quality Department.</li><li>Analyze clinical outcomes data, identify trends, and implement initiatives to enhance the quality of care.</li><li>Promote a culture of continuous quality improvement and evidence-based practice among all medical staff.</li></ul><p><b>Medical Staff Management &amp; Development:</b></p><ul><li>Serve as the primary administrative liaison for all physicians, fostering a collaborative and positive working environment.</li><li>Address and mediate professional practice concerns and conflicts.</li><li>Oversee the planning and accreditation of Continuous Medical Education (CME) and professional development programs for medical staff.</li></ul><p><b>Clinical Research &amp; Academia:</b></p><ul><li>Provide strategic direction and administrative support for the hospital's clinical research activities.</li><li>Foster partnerships with academic institutions and promote a research-oriented culture.</li><li>Ensure all research activities comply with ethical guidelines and regulatory requirements.</li></ul><p><b>Regulatory &amp; Accreditation:</b></p><ul><li>Act as the primary point of contact for all matters related to SCFHS and CBAHI.</li><li>Lead the preparation for and ensure successful passage of all national and international accreditation surveys.</li></ul><p><b>Qualifications &amp; Experience:</b></p><p><b>Essential:</b></p><ul><li>Medical Doctor (MD) or Bachelor of Medicine, Bachelor of Surgery (MBBS) degree from an accredited institution.</li><li>Valid SCFHS license and classification as a Consultant (or eligibility for the same).</li><li>Minimum of <b>10 years of post-qualification clinical experience</b>, with at least <b>5 years in a significant medical leadership or medical affairs role</b> within a large, acute care hospital.</li><li>Proven track record in medical governance, quality management, and accreditation processes (CBAHI, JCI, etc.).</li><li>Exceptional understanding of the Saudi Arabian healthcare landscape and regulatory framework.</li><li>Strong financial and budgetary management skills.</li><li>Outstanding leadership, communication, and interpersonal skills with the ability to influence and engage senior stakeholders.</li></ul><p><b>Desirable:</b></p><ul><li>Master's degree in Healthcare Administration (MHA), Business Administration (MBA), or a related field.</li><li>Experience in developing and launching clinical research programs.</li></ul><p>Job Type: Full-time</p>

CMO - Director of Medical Affairs

Qiddiya Investment Company

<div><p>Qiddiya Investment Company is looking for a detail-oriented Senior Specialist - Sponsorships to support our dynamic sponsorship team. In this critical role, you will be responsible for drafting, reviewing, and managing sponsorship contracts, ensuring compliance with legal standards and company policies. Your expertise will help facilitate successful and long-lasting partnerships that enhance our brand's presence in the entertainment and leisure sectors.</p><h3 class="jobSectionHeader"><b>
Responsibilities</b></h3><ul>
<li>Draft, review, and negotiate sponsorship contracts, ensuring clarity, compliance, and alignment with organizational goals.</li>
<li>Collaborate with stakeholders to understand sponsorship terms and develop agreements that reflect mutually beneficial arrangements.</li>
<li>Ensure all contracts adhere to legal standards and company policies, providing recommendations for any necessary modifications.</li>
<li>Maintain an organized repository of all contracts and relevant documentation, ensuring easy access and compliance tracking.</li>
<li>Work closely with the finance team to manage contract budgets, ensuring financial arrangements are accurately represented and adhered to.</li>
<li>Support the sponsorship team with legal inquiries, providing guidance on contract implications and best practices.</li>
<li>Assist in the evaluation and reporting of sponsorship contract performance metrics to inform future negotiations and strategy.</li>
<li>Stay updated on industry best practices, trends, and regulatory requirements related to sponsorship contracts.</li>
<li>Act as a liaison between internal departments and external partners to facilitate smooth contract implementation and address any issues that arise.</li>
</ul><p><b>Requirements</b></p><ul>
<li>Bachelor's degree in Law, Business Administration, or a related field.</li>
<li>4-6 years of experience in contract management or legal affairs, preferably within sponsorships or marketing.</li>
<li>Strong negotiation skills and a keen attention to detail in contract drafting and review.</li>
<li>Experience in identifying legal risks and providing effective solutions in contract negotiations.</li>
<li>Excellent written and verbal communication skills, with the ability to convey complex legal concepts in an understandable manner.</li>
<li>Strong organizational skills, with the ability to manage multiple contracts and deadlines simultaneously.</li>
<li>Proficiency in Microsoft Office and familiarity with contract management software.</li>
<li>Knowledge of sponsorship laws and regulations is an advantage.</li>
<li>Fluency in English is required; proficiency in Arabic is a plus.</li>
</ul><p><b>Benefits</b></p><p>
Comprehensive benefits package</p></div>

Senior Specialist - Sponsorships (COR441)

Takamol Holding

<div>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 We are seeking a highly skilled and strategic
 <strong>
  Senior Consultant in Public Policy
 </strong>
 to lead and support the development, evaluation, and implementation of public policy initiatives across priority sectors. The ideal candidate brings a strong background in evidence-based policy development, stakeholder engagement, and policy impact assessment, with the ability to translate complex issues into actionable, high-quality recommendations.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 <strong>
  Policy Advisory &amp; Design
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Lead the design and development of public policy solutions that align with national priorities and sectoral strategies.
  </li>
  <li>
   Provide high-level policy advisory support to government entities, institutions, and strategic partners.
  </li>
  <li>
   Synthesize research, best practices, and stakeholder input to inform policy recommendations.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Policy Analysis &amp; Research
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Conduct comprehensive policy analysis, regulatory reviews, and socioeconomic impact assessments.
  </li>
  <li>
   Oversee the production of policy briefs, white papers, and technical reports.
  </li>
  <li>
   Apply quantitative and qualitative research methodologies to inform decisions.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Stakeholder Engagement
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Facilitate consultation workshops, focus groups, and bilateral meetings with key stakeholders (government, private sector, civil society).
  </li>
  <li>
   Build and manage relationships with policy influencers, regulatory bodies, and international organizations.
  </li>
  <li>
   Ensure alignment across multi-stakeholder interests and coordinate policy consensus-building efforts.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Implementation &amp; Monitoring
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Develop actionable policy implementation plans with defined KPIs and milestones.
  </li>
  <li>
   Support policy rollout, change management, and capacity-building initiatives.
  </li>
  <li>
   Monitor and evaluate policy outcomes, and provide recommendations for adaptation or scaling.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Strategic Contributions
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Contribute to the development of public policy practice frameworks, methodologies, and strategic thought leadership.
  </li>
  <li>
   Mentor junior consultants and support proposal development, business growth, and strategic planning within the unit.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Preferred Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Experience advising senior government officials or high-level decision-makers.
  </li>
  <li>
   Exposure to policy areas such as labor markets, education, digital transformation, health, or climate.
  </li>
  <li>
   Experience with international organizations, development agencies, or think tanks is a plus.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Job Requirements
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree (or higher) in Public Policy, Economics, Political Science, Public Administration, or a related field.
  </li>
  <li>
   6+ years of relevant experience in public policy, strategy consulting, government affairs, or regulatory advisory.
  </li>
  <li>
   Demonstrated success in leading complex, multi-stakeholder policy projects.
  </li>
  <li>
   Strong analytical, writing, and communication skills, with fluency in English and Arabic.
  </li>
  <li>
   Deep understanding of policymaking processes, regulatory environments, and governance structures.
  </li>
 </ul>
</div>


Consulting Manager

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