elv engineer

engineering lead

lead electrical engineer

lead piping engineer

lead senior legal counsel

medical lead

Exceptional Medical Ambulance and Homecare Services LLC

We are seeking an experienced and highly competent Medical Director to lead and oversee all clinical operations across EMAHS. The ideal candidate will provide strong medical leadership, ensure compliance with UAE healthcare regulations, and maintain the highest standards of patient care across home care, emergency, and event medical services.Key Responsibilities<ul><li>Provide strategic leadership and direction for all medical and clinical operations.</li><li>Develop, implement, and monitor medical policies, clinical protocols, and best practices in alignment with regulatory and organizational standards.</li><li>Supervise, mentor, and support medical and nursing teams to ensure safe, effective, and high-quality patient care.</li><li>Coordinate with clients, event organizers, and operational teams to ensure medical readiness for home care assignments, events, and emergency deployments.</li><li>Review and approve medical documentation, incident reports, patient assessments, and transfer summaries.</li><li>Ensure full compliance with DHA/DOH/MOH regulations, licensing requirements, and quality benchmarks.</li><li>Lead training programs, simulations, and continuous professional development for clinical staff.</li><li>Contribute to strategic planning, budgeting, and resource allocation for the medical department.</li><li>Serve as a key advisor to management on clinical risk, quality improvement, and service expansion.</li></ul>Key Requirements<ul><li>MBBS / MD degree from a recognized institution (mandatory).</li><li>Valid UAE medical license or eligibility (DHA/DOH/MOH).</li><li>Minimum 5 years of total experience, including at least 2 years in home care and on-call medical services.</li><li>Prior experience in clinical leadership, emergency medical services, or event medical care is preferred.</li><li>Strong leadership, communication, and decision-making abilities.</li><li>Excellent organizational, analytical, and problem-solving skills.</li><li>Ability to lead effectively in a fast-paced, dynamic environment.</li></ul>Job Types: Full-time, Permanent

Medical Director – Healthcare & Event Medical Services

Allocation Assist DMCC

Role Overview
 We are seeking a highly experienced and patient-centered Consultant Neurologist to join a multidisciplinary team in Riyadh. The successful candidate will provide expert diagnosis, treatment, and long-term management of patients with a wide spectrum of neurological disorders, while contributing to clinical excellence, education, and research.
 
Key Responsibilities
 Conduct comprehensive neurological assessments and develop individualized treatment plans.
 Manage acute and chronic neurological conditions including stroke, epilepsy, Parkinson’s disease, multiple sclerosis, and migraine.
 Interpret neurodiagnostic tests such as MRI, CT, EEG, EMG, and lumbar punctures.
 Participate in multidisciplinary team (MDT) meetings and complex case discussions.
 Supervise and mentor junior physicians, residents, and fellows.
 Engage in clinical audits, research, and continuing medical education activities.
 Ensure compliance with SCFHS standards and hospital protocols.
 
Qualifications & Experience
 Medical Degree (MBBS or equivalent) from a recognized institution.
 Board Certification in Neurology (e.g., Saudi Board, Arab Board, American/Canadian Board, or European equivalent).
 Valid classification and registration with the Saudi Commission for Health Specialties (SCFHS) as a Consultant Neurologist.
 Minimum 3–5 years of post-specialization experience in clinical neurology.
 Proficiency in neuroimaging and neurophysiological diagnostics.
 Excellent communication, decision-making, and leadership skills.
 Fluency in English; Arabic proficiency is an asset.
 
Compensation & Benefits
 Competitive tax-free salary based on experience and qualifications.
 Fully furnished accommodation or housing allowance.
 Annual flight tickets for self and dependents.
 Comprehensive health insurance.
 CME allowance and support for professional development.
 End-of-service benefits as per Saudi labor law.

Neurologists -Lead in Riyadh’s Top Hospitals

Are you a passionate and highly skilled Emergency Medicine consultant looking for a new and exciting opportunity? Allocation Assist Middle East is seeking a Consultant Emergency Medicine to join one of the prestigious hospitals in Saudi Arabia.
 
Job Role: 
As a Consultant Emergency Medicine, you will play a vital role in the provision of high-quality emergency medical care to patients in Saudi Arabia. You will be responsible for diagnosing and treating acute and life-threatening conditions, providing timely and effective interventions, and coordinating with other medical professionals to ensure the best possible patient outcomes.
 
Key Responsibilities: 
<ul>
<li>Conduct initial assessments, examinations, and diagnoses of patients presenting to the emergency department</li>
<li>Implement effective and timely treatment plans to stabilize patients and prevent further deterioration</li>
<li>Communicate and collaborate with a multidisciplinary team to provide comprehensive care to patients</li>
<li>Oversee and supervise junior medical staff, providing guidance and mentorship as needed</li>
<li>Document all patient interactions and procedures accurately and in a timely manner</li>
<li>Participate in quality improvement initiatives and continuous professional development to maintain the highest standards of care</li>
</ul>
Requirements: 
<ul>
<li>Medical degree from an accredited institution</li>
<li>Board certification in Emergency Medicine from a recognized authority</li>
<li>Candidates must possess UK CCT, American Board, Canadian Board, or an equivalent certification.</li>
<li>Minimum of 5 years of post-graduate experience in Emergency Medicine</li>
<li>Previous experience in the Middle East is highly desirable</li>
<li>Excellent communication, interpersonal, and leadership skills</li>
<li>Fluent in English (Arabic proficiency is an advantage)</li>
</ul>
What We Offer: 
<ul>
<li>Competitive salary and benefits package</li>
<li>Relocation assistance and visa sponsorship</li>
<li>Professional development and training opportunities</li>
<li>Supportive and collaborative work environment</li>
<li>Opportunity to make a difference in the lives of patients and contribute to the development of healthcare in Saudi Arabia</li>
</ul>
If you are a dedicated and highly motivated Emergency Medicine consultant ready to take on a challenging yet rewarding role, we want to hear from you! Apply and be a part of the team and make a positive impact in the healthcare industry in Saudi Arabia.

Lead Emergency Care in the Kingdom’s Top Hospitals

Takeda Pharmaceuticals

<div>By clicking the &ldquo;Apply&rdquo; button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda&rsquo;s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.<h2 class="jobSectionHeader">
Job Description</h2>
OBJECTIVES/PURPOSE<ul><li>
Defines, develops, and leads area regulatory strategies, in close alignment with line management and Country (LOC) RA Heads, to maximize regulatory success and enabling patient access, including all aspects of submission and timely approval of investigational drugs, marketing authorizations and life-cycle management submissions and subsequent Q&amp;As from authorities. &ldquo;</li><li>
Effectively communicates (including Global Product Team (GPT) representation when relevant) the regulatory strategies, submission plans and timelines; assessment of the likelihood of success of regulatory strategies and impact assessments of trends, regulations and changes related to assigned programs.</li><li>
Liaise with cross functional stakeholders including Global Regulatory Teams (GRT) to represent GEM RA strategies</li><li>
Additionally may act as GEM RA Lead for one or more assets for entire GEM region covering from development to the life cycle maintenance activities.</li><li>
Provides strategic and tactical advice, guidance and area regulatory expertise to global leadership teams on how to achieve timely and efficient conduct of development and/or life-cycle management of assigned programs while maintaining full compliance with applicable regulatory requirements</li><li>
Leads the Submission Working Group (SWG) for submissions in the area and represents the area as needed on global and project teams for the new Mas &amp; other major submissions</li><li>
Manages or supports and oversees interactions with Health Authorities in the Area in collaboration with Area stakeholders and LOC RA teams</li><li>
May support value and access team in their interactions with Health Authorities for negotiations related to products within their responsibility (wherever applicable) &ndash; For specific areas only</li><li>
Evaluates new business development opportunities and / or participates in due diligence teams</li><li>
May act as Deputy of RA Area Head and may support RA activities for other areas as needed</li></ul>
ACCOUNTABILITIES<ul><li>
Demonstrates Takeda leadership behaviors at all times (for external need HR support to briefly highlight Takeda leadership behaviours requirements)</li><li>
Independently manages, plans, and works closely with Regional, LOC Regulatory Leads, BU Cross-functional Teams (CFT), and Global Regulatory Teams to deliver all aspects of regulatory activities throughout the product life cycle in close partnership with Global Regulatory TA Leadership and aim for a successful and timely outcome of RA applications in the area</li><li>
Oversees and accountable for working with other RA functions and/or vendor to ensure that regulatory submissions and approvals are achieved on schedule within area of responsibility</li><li>
Accountable for communications to the regulator, development teams, and GRA, other Research and Development (R&amp;D) functions, and TAU leadership.</li><li>
Provides regulatory expertise on drug development, registration and / or post-marketing compliance and life cycle management.</li><li>
Participates, as appropriate, and authors/reviews internal procedures and processes.</li><li>
Understands and interprets complex scientific issues for products of responsibility as it relates to regulatory requirements and strategy.</li><li>
Develops effective working relationships with LOC Regulatory Lead, Regional and Global Regulatory Team, cross- functional commercial Area &amp; LOC Teams; company&rsquo;s consultants and Business Partners as required.</li><li>
Actively pursues or oversees the tracking and fulfillment of post- marketing commitments.</li><li>
Presents regional regulatory strategies to leadership/senior management and shall be able to identify and share the risks and opportunities as well as probability of success of proposed strategy</li></ul>
DIMENSIONS AND ASPECTS
Technical/Functional (Line) Expertise<ul><li>
Solid regulatory experience, including knowledge of regulations and guidance applicable in the region across all phases of development and able to orient project teams in the interpretation of guidelines; an understanding of basic regulatory requirements in other regions globally (US, EU, emerging markets) is a plus.</li><li>
 Understands the essentials of evidence requirements beyond marketing authorization (i.e. in support of patient access/ tender requirement)</li><li>
Able to formulate regional regulatory strategy to achieve competitive and accelerated product approvals</li><li>
Experience of initial MA, indication/ line extension applications and/or lifecycle management and development submissions</li><li>
Experience with advanced therapeutic medical products (Cell &amp; gene therapy) will be advantageous</li></ul>
Leadership<ul><li>
Able to manage with limited supervision different types of regulatory development or lifecycle management procedures in the region in coordination with the LOC RA teams.</li><li>
Stays current with regulations / guidance in the region for impact on drug development plans, registration, and life-cycle management to maximize the positive outcomes of the regulatory applications and maintain regulatory compliance.</li><li>
Acts as an ally to support individuals as a whole and promotes an inclusive culture</li><li>
Practices active listening, encourages open dialogue, feedback, and diverse opinions</li><li>
Can speak up and is perceived as a natural, assertive authority whom peers trust for their advice</li></ul>
Decision-making and Autonomy<ul><li>
Is able to prioritize activities and execute within reasonable time with limited supervision</li><li>
Can take some tactical decisions independently</li></ul>
Interaction<ul><li>
Experience of participating or leading interaction with Health Authorities</li><li>
Communicates externally/with authorities in concise and respectful language</li><li>
Adapts to changing circumstances and is able to build and maintain relationships with Global teams and LOC RA and other CFTs</li><li>
Has their voice heard as remote participant to global or cross functional teams (GRT, GPT etc); influences meeting agendas &amp; outcomes to optimally integrate regional strategic needs</li></ul>
Complexity (Products managed, mix of businesses, internal and/or external business environment, cultural considerations)<ul><li>
Self-aware and able to function effectively while meeting the multiple challenges with a sense of energy, vitality, and confidence</li><li>
Develops concise strategic plans, understandably outlines the opportunities and risks of alternative scenarios before proposing a decision</li></ul>
EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:<ul><li>
BSc. Advanced scientific related degree preferred; BA accepted based on experience.</li><li>
A minimum of 8 years of experience in drug regulatory affairs preferably within the EU/GEM region.</li><li>
Prior experience of &lsquo;area&rsquo;/ countries will be an advantage</li><li>
Receives and gives feedback; expresses ideas, questions, and disagreement</li><li>
Fluency in English and other local languages will be an advantage</li><li>
Work in flexible hours</li></ul><h2 class="jobSectionHeader">
Locations</h2>
Dubai, UAE<h2 class="jobSectionHeader">
Worker Type</h2>
Employee<h2 class="jobSectionHeader">
Worker Sub-Type</h2>
Regular<h2 class="jobSectionHeader">
Time Type</h2>
Full time</div>

GEM Regulatory Leads - EAMEA

AstraZeneca

<div>JOB TITLE
Medical Manager Oncology &ndash; Gulf 
 
ABOUT ASTRAZENECA
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world&rsquo;s most serious diseases. But we&rsquo;re more than one of the world&rsquo;s leading pharmaceutical companies.
ROLE SUMMARY
An office-based role couple with strong external scientific leadership and partnership. Medical Manager is responsible in leading a high-performing Field Medical team that drives enhanced patient outcomes and the safe and effective use of AstraZeneca medicines with prioritization according to company strategy and organizational impact. The role ensures excellence in execution, and leverages innovations wherever appropriate, of the local Medical Affairs strategic plans through the Field Medical team composed of confidence and evidence generation activities.
Medical Manager has a deep understanding of the local healthcare system, its priorities, and challenges and lead the team with an Integrated Engagement plan to gather insights, foster scientific and strategic partnerships with major hospitals, institutions/ authorities and non-traditional stakeholders (E.g. policy and decision makers, payer groups, government, researchers and other) and drive fundamental and sustainable clinical practice transformations in alignment with the Medical Affairs strategy and the company&rsquo;s portfolio that strengthen healthcare ecosystems, improve treatment outcomes, that enable patient access to quality care.
Acts as a manager, coach, and leader to the field medical team, Medical Manager provides operational guidance along with skills &amp; capabilities training in accordance with the Global/local standards and relevant job descriptions. The role is responsible for performance management, operational excellence, driving impact and efficiencies through measurable outcomes and a continuous improvement approach and communicating the quality delivery and value of the Medical Affairs team with good understanding of the internal business ecosystem (strategy, model, finances). Medical Manager acts as a key member of the local Medical Affairs team and Cross-functional Brand team that contributes to the planning and execution of Medical Affairs strategies, working closely with the local medical and cross-functional teams.
What you&rsquo;ll do
Team &amp; People Management:<ul><li>
Recruit the right talent based on capabilities and abilities required for the field medical role.</li><li>
Ensure the optimal environment for the MSL development, growth, and high performance.</li><li>
Foster a culture of I&amp;D, agility, innovative mindset, win-win partnerships and collaboration.</li><li>
Lead an effective, strategic, and outcomes-oriented field medical team with a high level of scientific expertise.</li><li>
Manage and drive team&rsquo;s performance with measures and metrics put in place that reflect meaningful patient outcomes with continuous improvement approach.</li><li>
Lead a team with comprehensive understanding of the healthcare ecosystem to address population health discussions and deliver outcomes that address impact across the patient pathway.</li><li>
Guide the team to have a deep understanding of stakeholder needs to effectively communicate complex scientific information using the right content and channel mix.</li><li>
Ensure the team&rsquo;s quality and promptness of status, information and insights reported back to the cross-functional teams and in company tracking systems.</li><li>
Role model as an expert in the assigned therapeutic area with well established relationships with key healthcare professionals.</li><li>
Conduct one on one meetings/field visits to coach and review according to the most up-to-date global field medical engagement model on proficiency and related capabilities.</li><li>
Role model the AstraZeneca values fostering personal accountability, ownership of individual and team success, operational agility and growth mindsets.</li><li>
Contributes to establishing and implementing policies, procedures and objectives for own work and for the field medical team(s).</li><li>
Lead and manage change initiatives as needed in the field to enable positive business outcomes.</li><li>
Oversee regular monitoring, checks and education to ensure direct reports&rsquo; compliance with all AstraZeneca guidelines, standards, policies and local regulations.</li><li>
Manages and oversees team financial resources.</li></ul>
Strategic Planning and Delivery:<ul><li>
Ensure the Field Medical Strategic Plan (FMSP) and MSL activities are prioritized, aligned with the Medical Affairs Strategic Plans, and executed with excellence and according to budget and timelines.</li><li>
Ensure the Field Medical Plan includes an Integrated Engagement plan with an appropriate ratio of traditional and non-traditional stakeholders.</li><li>
Drive the identification of prioritized cross functional accounts in focus for VTC for the AZ therapeutic area/ medications. Foster scientific and strategic partnerships with KEEs to transform medication/ healthcare ecosystems, improve treatment outcomes, that enable patient access to quality care.</li><li>
Work closely with the Medical Affairs Team and cross functional team to provide input to medical and brand strategies.</li><li>
Works as a strategic partner of the value team (E.g. Marketing and Market Access) to identify clinical and payer data gaps and evidence generation needs.</li><li>
Contributes to BSP process by providing scientific and medical inputs to the development and evaluation of local operational brand strategy, including KEEs, customer insights and competitive intelligence. Identify opportunities and initiate discussion potential strategic, scalable &amp; sustainable clinical practice transformations initiatives that can impact on patient access to quality care.</li><li>
Drives prioritization of activities across the team to ensure appropriate focus on portfolio priorities, including pre-launch and launch excellence.</li><li>
Ensures the team leverages Digital and innovation/ technology as an enabler for patient centric solutions and effectively contributes to enhancing equitable access to people in assigned accounts/ clinics/ healthcare systems.</li><li>
Leverage technology, available data/ dashboards to drive data-driven decisions to support internal discussions and external engagements.</li><li>
Contribute on field and external stakeholder insights and perspectives in medical and brand internal strategic discussions and communicate internally on actionable items regularly.</li><li>
Provide regular updates to team and broader organization on delivery versus plan, variance to plan, proposed mitigation with emphasis on internal &amp; external strategic and patient impact.</li><li>
Ensures own knowledge of therapeutic area, best practices, relevant scientific peer-reviewed literature, and new relevant developments are kept up to date with understanding of its relevance to the team(s).</li><li>
Responsible for allocating resources for sales force medical training.</li><li>
Lead national/ cluster advisory board meetings and other above-cluster activities, if necessary.</li><li>
Manage Real World Evidence Projects including observational studies, local data collection and others.</li></ul>
Corporate responsibility and Medical Information and Governance:<ul><li>
Review activities and materials to ensure compliance with internal and industry policies and procedures.</li><li>
Respond to unsolicited Medical Information (MI) requests about approved and unapproved AstraZeneca products, or about unapproved uses of approved AstraZeneca products in an objective, well balanced, substantiated manner that is scientific in tone and content, free of promotional messages, truthful, and is not misleading.</li><li>
Demonstrate appropriate response and documents the provision of accurate, scientific data in response to unsolicited scientific questions posed by healthcare providers with Company Policies, and applicable laws, regulations, and ethical standards.</li><li>
May lead in the management of medical information and pharmacovigilance within a particular market.</li><li>
Ensure compliance with AZ Code of Ethics, corporate governance, audit requirements, guidelines, industry codes, policies and procedures, and discloses potential breach.</li><li>
Ensure that company confidentiality is maintained (i.e. intellectual property, product, strategic and salary information)</li><li>
Ensure that all conducted activities are done in accordance with local legislation and corporate standards.</li><li>
Report health/ environment/ wellbeing related accidents, adverse events, and conflict of interest as per respective procedures and on a timely manner.</li></ul>
Essential for the role<ul><li>
Bachelor&rsquo;s degree in medicine or pharmacy is required</li><li>
Post-graduate master&rsquo;s degree is an advantage</li><li>
Experience in Oncology area is preferable</li><li>
Minimum of 4 years of experience in Medical Affairs role including 1 year of people management experience</li><li>
Excellent oral and written communication and interpersonal skills</li><li>
Excellent Project Management and presentation skills</li><li>
Advanced level analytical and conceptual thinking</li><li>
Thorough knowledge and experience of the pharmaceutical industry and the field medical function</li><li>
Ability to interact and manage a range of stakeholders both internally and externally.</li><li>
Knowledge of legislation relevant to pharmaceutical industry</li></ul>
Desirable for the role<ul><li>
Doctoral degree in a scientific discipline (e.g. M.D., Ph.D., Pharm.D.)</li><li>
Experience in clinical or pre-clinical research and knowledge of therapuetic area disease state and treatment.</li><li>
Experience in basic research, drug discovery and drug development.</li><li>
Understanding of multiple aspects within Medical Affairs department</li><li>
Team Management experience</li></ul>
Why AstraZeneca?
At AstraZeneca we&rsquo;re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There&rsquo;s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We&rsquo;re on an exciting journey to pioneer the future of healthcare. 
So, what&rsquo;s next?
<ul><li>Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.</li><li>
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it&rsquo;s yours.</li></ul>
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
Follow AstraZeneca on Facebook
Follow AstraZeneca on Instagram</div>

Medical Manager – Oncology, Gulf

Role Overview
 A top-tier hospital in Dubai is seeking a highly skilled Consultant in Pediatric Intensive Care to lead its state-of-the-art PICU. The role involves managing critically ill pediatric patients with complex medical and surgical conditions, using advanced life-saving interventions and a multidisciplinary approach.
 
Key Responsibilities
 <ul>
<li>Deliver expert care to high-acuity pediatric patients in the PICU</li>
<li>Perform advanced procedures: mechanical ventilation, ECMO, invasive monitoring</li>
<li>Collaborate with pediatricians, surgeons, nurses, and allied health professionals</li>
<li>Design individualized treatment plans and monitor patient progress</li>
<li>Mentor junior staff and contribute to clinical education programs</li>
<li>Lead quality improvement initiatives and uphold international care standards</li>
<li>Participate in clinical research and stay current with PICU advancements</li>
</ul>
Qualifications & Experience
 <ul>
<li>Medical degree (MD or equivalent) from a recognized institution</li>
<li>Board certification in Pediatric Intensive Care / Pediatric Critical Care Medicine</li>
<li>Western training (USA, UK, Canada, or equivalent) is mandatory</li>
<li>Minimum 3–5 years post-board experience in a consultant PICU role</li>
<li>Proven expertise in advanced pediatric critical care techniques</li>
<li>Strong leadership, communication, and family-centered care philosophy</li>
<li>Eligible for DHA Consultant licensure (Dubai Health Authority)</li>
</ul>
Compensation & Benefits
 <ul>
<li>Tax-free salary: AED 80,000–90,000/month</li>
<li>Performance-based incentives</li>
<li>Comprehensive family medical insurance</li>
<li>Housing and transportation allowance</li>
<li>Relocation support for international candidates</li>
<li>Access to cutting-edge PICU technologies and training programs</li>
</ul>

Lead Pediatric Critical Care - PICU Roles in Dubai

Explore 3298+ Medical lead in Dubai this December. Find roles across top companies and apply now to boost your career.

3298 medical lead jobs IN Dubai

Medical Director – Healthcare & Event Medical Services

Neurologists -Lead in Riyadh’s Top Hospitals

Lead Emergency Care in the Kingdom’s Top Hospitals

Lead Emergency Care in the Kingdom’s Top Hospitals

GEM Regulatory Leads - EAMEA

Medical Manager – Oncology, Gulf

Lead Pediatric Critical Care - PICU Roles in Dubai