clinical haematologist

Allocation Assist DMCC

Role Overview
 We are seeking a highly qualified Consultant Hematologist with expertise in benign hematological disorders to join a leading healthcare institution in Dubai. The ideal candidate will provide comprehensive diagnostic and therapeutic services, contribute to multidisciplinary care, and support clinical governance and education initiatives.
 
Key Responsibilities
 <ul>
<li>Diagnose and manage benign hematological conditions, including anemia, thrombocytopenia, leukopenia, bleeding disorders, and hemoglobinopathies.</li>
<li>Interpret bone marrow biopsies, peripheral blood smears, and hematological lab investigations.</li>
<li>Collaborate with internal medicine, oncology, and transfusion services for integrated patient care.</li>
<li>Participate in multidisciplinary team meetings and case discussions.</li>
<li>Contribute to clinical audits, quality improvement, and evidence-based practice.</li>
<li>Engage in teaching and mentoring junior doctors and allied health professionals.</li>
</ul>
Qualifications & Experience
 <ul>
<li>MBBS or equivalent medical degree</li>
<li>Completion of specialist training in Hematology (e.g., CCT, FRCP, FRCPath, American Board, or equivalent)</li>
<li>Minimum 5 years post-specialization experience in benign hematology</li>
<li>DHA eligibility or licensure preferred</li>
<li>Strong interpersonal and communication skills</li>
<li>Fluency in English; Arabic is an asset</li>
</ul>
Desirable Attributes
 <ul>
<li>Experience in outpatient and inpatient hematology services</li>
<li>Familiarity with regional hematological profiles (e.g., thalassemia, iron deficiency)</li>
<li>Interest in clinical research or academic collaboration</li>
</ul>

Consultant Hematologist (Benign) - Dubai

Role Overview
 We are seeking a highly qualified and culturally attuned Consultant Hematologist to join a leading tertiary care hospital in Abu Dhabi. The ideal candidate will bring deep expertise in diagnosing and managing both benign and malignant hematologic disorders, with a strong commitment to evidence-based care and multidisciplinary collaboration.
 
Key Responsibilities
 
Diagnose and manage hematologic conditions, including: 
<ul>
<li>Anemia, thrombocytopenia, leukemias, lymphomas, myeloma</li>
<li>Hemophilia, sickle cell disease, and clotting disorders</li>
<li>Oversee bone marrow biopsy procedures, transfusion protocols, and chemotherapy regimens</li>
<li>Collaborate with oncology, pathology, and radiology teams for integrated patient care</li>
<li>Provide consultative services to inpatient and outpatient units</li>
<li>Participate in tumor boards, clinical audits, and quality improvement initiatives</li>
<li>Educate patients and families on disease management and treatment plans</li>
<li>Contribute to academic teaching and CME programs</li>
</ul>
Qualifications & Experience
 <ul>
<li>Certification: Board-certified in Hematology (e.g., American Board, Royal College, or equivalent)</li>
<li>Licensure: DOH (HAAD) license or eligibility required</li>
<li>Experience: Minimum 5 years post-specialization in a tertiary or academic hospital setting</li>
<li>Proven expertise in both benign and malignant hematologic conditions</li>
<li>Strong diagnostic, procedural, and communication skills</li>
</ul>
Compensation & Benefits
 <ul>
<li>Competitive tax-free salary (AED 70,000–90,000/month depending on experience)</li>
<li>Annual performance bonus</li>
<li>Housing allowance or furnished accommodation</li>
<li>Family medical insurance</li>
<li>CME allowance and paid study leave</li>
<li>Relocation support and visa sponsorship</li>
</ul>

Dubai’s Demand for Skilled Female Hematologists

Consultant Hematologist (Female) - Abu Dhabi

Hematologists in Abu Dhabi - Expert Blood Disorder Care

Amigo

<div>
 
 About Amigo
 
 
 
 Amigo builds AI agents for healthcare&mdash;systems that handle patient conversations, take clinical actions, and escalate to humans when needed.
 
 
 Clinical research focuses on healthcare-specific problems: evaluation frameworks for clinical safety, methods for learning what works across patient populations, and ensuring agent behavior meets the standards healthcare organizations require.
 
 
 Series A from leading investors. Clinical validation and evidence generation in partnership with leading academic medical institutions.
 
 
 
 About This Role
 
 
 
 As a Clinical Research Scientist at Amigo, you'll lead research on clinical AI safety, evaluation frameworks, and evidence generation. You'll design studies that validate agent performance across patient populations, develop metrics for clinical quality, and publish findings that advance the field. Your clinical expertise ensures our agents meet the standards required for autonomous operation in healthcare.
 
 
 This role bridges clinical practice and AI research. You'll work directly with our agent engineering and data science teams to translate clinical knowledge into measurable evaluation criteria and safety guardrails.
 
 
 
 What You'll Do
 
 
 
 <ul>
 <li>
 Design and lead clinical validation studies for AI agent performance
 </li>
 <li>
 Develop evaluation frameworks and metrics for clinical safety and quality
 </li>
 <li>
 Publish research on clinical AI safety and agent evaluation methodologies
 </li>
 <li>
 Collaborate with academic medical institutions on research partnerships
 </li>
 <li>
 Define clinical protocols and escalation criteria for agent behavior
 </li>
 <li>
 Review agent outputs and failure modes from a clinical perspective
 </li>
 <li>
 Contribute to regulatory submissions and compliance documentation
 </li>
 <li>
 Advise on clinical workflow design and patient safety considerations
 
 
 </li>
 </ul>
 
 What We're Looking For
 
 
 
 <ul>
 <li>
 MD or equivalent medical degree with active clinical license
 </li>
 <li>
 Clinical experience in primary care, internal medicine, or relevant specialty
 </li>
 <li>
 Track record of clinical research and peer-reviewed publications
 </li>
 <li>
 Understanding of clinical quality metrics and patient safety frameworks
 </li>
 <li>
 Experience with clinical study design and IRB processes
 </li>
 <li>
 Ability to translate clinical expertise into technical requirements
 </li>
 <li>
 Strong communication across clinical, research, and engineering teams
 </li>
 <li>
 Interest in AI/ML applications in healthcare
 
 
 </li>
 </ul>
 
 Nice to have
 
 
 
 <ul>
 <li>
 Fellowship or additional training in clinical informatics
 </li>
 <li>
 Experience with digital health or health technology companies
 </li>
 <li>
 Background in quality improvement or patient safety initiatives
 </li>
 <li>
 Familiarity with FDA guidance on clinical decision support and AI/ML
 </li>
 <li>
 Experience with EHR systems and clinical workflow optimization
 </li>
 <li>
 Publications in clinical AI, digital health, or health informatics
 
 
 </li>
 </ul>
 
 Benefits
 
 
 
 Health &amp; Wellness
 
 
 <ul>
 <li>
 Comprehensive health, dental, and vision insurance
 </li>
 <li>
 Mental health support and wellness coaching
 </li>
 <li>
 Flexible wellness stipend for fitness, therapy, or personal growth
 </li>
 <li>
 Daily catered lunch and dinner
 
 
 </li>
 </ul>
 Growth &amp; Development
 
 
 <ul>
 <li>
 Annual learning budget for courses, books, or conferences
 </li>
 <li>
 Conference attendance budget for professional development
 </li>
 <li>
 Development setup of your choice
 </li>
 <li>
 Academic collaboration opportunities
 
 
 </li>
 </ul>
 Compensation Range: $150K - $300K
 
 
</div>

Research Scientist (Clinical)

Advanced Clinical

<div>
 
 
 Clinical Scientist Data Reviewer
 
 
 
 
 6 month contract w/ renewal
 
 
 
 
 3 days onsite in Jersey City, NJ
 
 
 
 
 
 
 We are seeking a Clinical Scientist Data Reviewer that will support the scientific planning efforts and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate technical skills and scientific acumen as part of a cross-functional clinical development team. You will be a key contributor and supporter in the clinical science activities of evidence generation for regulatory approval and/or engagement with physicians, including protocol development, study implementation, data analysis and reporting of results. This role will be focused on the detailed and critical safety data review efforts from study start-up through final CSR. The Clinical Scientist Data Reviewer is a crucial role in analyzing and interpreting clinical trial data to ensure accuracy, integrity, and compliance with regulatory requirements. There is additional room for growth and leadership opportunities in this role.
 
 
 
 
 
 Responsible for supporting specific aspects of clinical/scientific execution of clinical protocol(s). This may include:
 
 <ul>
 <li>
 Serving as a supportive clinical scientist data reviewer focused on safety, efficacy and critical data deliveries as part of the clinical trial team
 </li>
 <li>
 Supporting the clinical study team as part of the clinical sciences functional line which is closely aligned with the medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with Clinical Research and Pharmacovigilance (as well as other functional areas in this matrix environment)
 </li>
 <li>
 Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); partnering with Clinical Operations on critical and key study deliverables
 </li>
 <li>
 Ensure CRF design supports data collection in alignment with the Protocol in collaboration with Clinical Data Management/Programming
 </li>
 <li>
 Collaborating cross-functionally to review clinical data to ensure quality, completeness, and integrity of trial conduct
 </li>
 <li>
 Potential to provide tactical/scientific mentorship to other clinical scientists and move into Clinical Scientist lead role as well as focus on scientific growth and development
 </li>
 <li>
 Responsible for assisting with the generation, analysis, and presentation of clinical data, including manuscripts, abstracts, and oral presentations (including authoring documents and slide preparation as appropriate)
 </li>
 <li>
 Apply proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; identifies risks and designs mitigation strategies
 </li>
 <li>
 Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 <ul>
 <li>
 6+ years of experience with a Post Graduate Degree or 8+ years of experience with a Bachelor&rsquo;s degree in a relevant scientific discipline.
 </li>
 <li>
 Experience in clinical drug development experience, or a PhD, Pharm D, or RN degree is preferred.
 </li>
 <li>
 Experience within oncology preferred
 </li>
 <li>
 Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
 </li>
 <li>
 Ability to manage multiple competing priorities with good planning, time management and prioritization skills
 </li>
 <li>
 Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions
 </li>
 <li>
 Proficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents related to clinical trials, such as medical monitoring plan, SAPs, informed consent and clinical components of the Clinical Study Reports
 </li>
 <li>
 Interact with key stakeholders across Clinical Development functional areas
 </li>
 <li>
 Role requires proactive approach, strategic thinking and leadership in driving toward clinical study goals
 </li>
 <li>
 Influence opinions and decisions of internal and external customers / vendors, across functional areas
 </li>
 <li>
 Problem solving, prioritization, conflict resolution and critical thinking skills
 </li>
 <li>
 Strong communication, technical writing, and presentation skills experience
 </li>
 </ul>
 
 
</div>

Clinical Scientist Data Reviewer

MountainView Regional Medical Center

<div>Job Summary 
 
The Clinical Resource Analyst supports the implementation, optimization, and maintenance of clinical information systems to improve patient care delivery and operational efficiency. Acting as a key liaison between clinical users and IT teams, this role ensures that Electronic Health Records (EHR), Laboratory Information Systems (LIS), Radiology Information Systems (RIS), and other clinical platforms meet organizational standards and align with real-world clinical workflows. The Clinical Resource Analyst plays a critical role in translating clinical needs into technical solutions, troubleshooting system issues, supporting system integration, and providing end-user training and support. 
 
Essential Functions<ul><li>
Supports the configuration, maintenance, and optimization of clinical applications including EHR, LIS, RIS, and other ancillary systems.</li>
<li>Coordinates with clinical and IT stakeholders to implement new systems, updates, or enhancements and ensures alignment with clinical workflows.</li>
<li>Performs system testing (unit, integration, and user acceptance testing) to validate system functionality and support go-live activities.</li>
<li>Monitors system performance and collaborates with IT to identify and resolve technical issues, bugs, or downtime affecting clinical operations.</li>
<li>Conducts workflow analyses to assess efficiency, identify opportunities for improvement, and support the redesign of processes through technology.</li>
<li>Assists with build and maintenance of the clinical content within systems (e.g., clinical decision support, order sets, templates, CDM updates).</li>
<li>Supports data integrity and quality by ensuring system configurations comply with clinical standards, regulatory requirements, and privacy laws.</li>
<li>Serves as a subject matter resource for clinical system users, providing guidance, training, and documentation to support adoption and effective use.</li>
<li>Collaborates with departments on data reporting needs, pulling and analyzing data to support quality initiatives and clinical decision-making.</li>
<li>Facilitates communication between clinical departments and IT to ensure issues are escalated appropriately and resolved in a timely manner.</li>
<li>Ensures seamless integration between clinical systems and other healthcare technologies, including lab, radiology, and pharmacy systems.</li><li>
Performs other duties as assigned.</li>
<li>Maintains regular and reliable attendance.</li>
<li>Complies with all policies and standards.</li></ul>
Qualifications<ul><li>
Bachelor's Degree in Healthcare, Health Informatics, Information Technology, Nursing, or a related field preferred
</li><li>2-4 years of experience implementing and supporting clinical information systems required
</li><li>1-3 years of clinical experience in an acute care or patient care setting required
</li></ul>Knowledge, Skills and Abilities<ul><li>
In-depth knowledge of EHR platforms (e.g., Epic, Cerner, Allscripts) and their implementation, configuration, and optimization.</li>
<li>Familiarity with healthcare interoperability standards such as HL7, FHIR (Fast Healthcare Interoperability Resources), and DICOM (Digital Imaging and Communications in Medicine).</li>
<li>Understanding of how CDSS tools are used in clinical settings to improve decision-making and patient care.</li>
<li>Proficiency in querying clinical databases and understanding how to manipulate clinical data for reporting and analysis.</li>
<li>Familiarity with data analysis and reporting tools, such as Tableau, Power BI, or Crystal Reports, to provide insights based on clinical data.</li>
<li>Strong understanding of the Health Insurance Portability and Accountability Act (HIPAA) to ensure compliance with data privacy and security regulations.</li>
<li>Familiarity with other healthcare regulations and standards such as ICD-10, CPT, and SNOMED.</li>
<li>Ability to diagnose system issues, analyze clinical workflows, and implement solutions that improve system performance and user experience.</li>
<li>Strong ability to communicate technical concepts to non-technical clinical staff and translate clinical needs into technical requirements.</li>
<li>Ability to collaborate with clinical teams, IT staff, vendors, and other stakeholders to implement and maintain effective clinical systems.</li></ul>
Licenses and Certifications<ul><li>
CPHIMS - Certified Professional in Healthcare Information and Management Systems preferred</li></ul></div>

Clinical Resource Analyst

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