clinical coder

Sidra

<div><p><div><div><div><div><div><div><div><b>JOB SUMMARY<br>
</b></div></div></div></div></div><br>
<div><div><div><div><div>A Clinical Coder is a skilled medical professional responsible for accurately coding medical diagnoses, procedures, and services. The role requires expert-level knowledge of clinical coding systems, including but not limited to ICD-10-CM, CPT-4, HCPCS, and LOINC. The Clinical Coder must have a strong understanding of human anatomy and physiology to interpret medical classifications and accurately assign codes for various patient encounters, including outpatient, inpatient, emergency, and daycare visits.
</div></div><div><div>Key responsibilities include coding all diagnostic, laboratory, radiology, operative, surgical, office procedures, evaluation and management (E/M) services, and consultation codes from medical records using standardized classification systems for all encounters type i.e Outpatient , Inpatinet , daycare ,pharmacy, emergency. The Clinical Coder independently performs quality checks on their own work, ensuring accuracy and compliance with coding guidelines.
</div></div><div><div>The Clinical Coder is also responsible for <b>concurrent coding </b>, reviewing medical records in real-time during a patient&rsquo;s hospitalization for all encounters types to ensure accurate documentation, coding, and charge capture before discharge. This proactive approach improves billing accuracy, minimizes delays, and supports efficient claims processing.
</div></div><div><div>For inpatient cases, the Clinical Coder determines the appropriate Diagnosis-Related Group (DRG) to optimize hospital reimbursement ethically and in accordance with approved coding conventions. The role involves reviewing and analyzing medical records to extract relevant data and ensure precise code assignment, supporting accurate case mix classification and optimal financial outcomes.
</div></div><div><div>Additionally, the Clinical Coder plays a crucial role in <b>charge capture </b>, ensuring that all billable services and procedures are correctly recorded and appropriately linked to the patient&rsquo;s account. By validating and reconciling charges against clinical documentation, they help prevent revenue loss and billing discrepancies.
</div></div><div><div>The Clinical Coder collaborates closely with departments such as Quality, Finance, Revenue Cycle, Registration, Scheduling, Case Management, and Compliance to resolve coding and billing issues. They investigate and address problems, complaints, and incidents related to coding and assist the Coding Manager in resolving such matters efficiently.</div></div></div></div></div></div></div></p></div>
<br><div><div>About US</div>
<div><div>Sidra Medicine a healthy population is essential to a strong, prosperous society, and throughout 2020, Sidra continued to provide uninterrupted comprehensive specialist healthcare services for children and young people; and exceptional maternity, gynecology, and reproductive medical services for women, previously unavailable in Qatar and the region.&rdquo; &ndash; H.H Sheikha Moza bint Nasser, Chairperson of Qatar Foundation
</div><div>Sidra Medicine represents the vision of Her Highness Sheikha Moza bint Nasser who serves as its Chairperson. This high-tech facility is home to world-class patient care, scientific expertise, and educational resources.</div></div></div><div></div>

Clinical Coder

DOC Medical Center

<div>
 DOC Medical Center is seeking an experienced Insurance Manager responsible for leading the insurance function, streamlining patient insurance claims and recovery processes, and ensuring effective coordination with insurance companies. The role is accountable for optimizing reimbursements, enhancing patient satisfaction, overseeing insurance operations, and developing, implementing, and monitoring insurance policies, protocols, and best practices across the organization.
 <br/>
 <br/>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 Educational qualification: MBBS/BDS/B. Sc. Nursing/B. Pharm
 <br/>
 <br/>
 15+ years of healthcare insurance experience within Qatar and/or GCC countries.
 <br/>
 <br/>
 Minimum 5 years in a managerial/supervisory role
 <br/>
 <br/>
 CPC (Certified Professional Coder) certification preferred but not mandatory
 <br/>
 <br/>
 Strong knowledge about medical insurance system within state of Qatar
 <br/>
 <br/>
 Proven leadership, analytical, and negotiation skills
 <br/>
 <br/>
 Familiarity with insurance software
 <br/>
 <br/>
 Good understanding of insurance management, requirement and dynamics.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 Lead end-to-end insurance operations, claims administration, and payer management.
 <br/>
 <br/>
 Manage provider agreements, contract negotiations, and insurance network relationships.
 <br/>
 <br/>
 Oversee claims submission, adjudication follow-up, reconciliations, and reimbursement optimization.
 <br/>
 <br/>
 Monitor claim denials, disallowances, resubmissions, and revenue recovery performance.
 <br/>
 <br/>
 Ensure compliance with payer policies, regulatory requirements, and insurance protocols.
 <br/>
 <br/>
 Lead and develop the insurance team to achieve claims and revenue cycle targets.
 <br/>
 <br/>
 Analyze insurance KPIs, rejection trends, and payer performance metrics.
 <br/>
 <br/>
 Collaborate with Finance and Revenue Cycle teams to improve collections and reduce write-offs.
 <br/>
 <br/>
 Drive process improvements, operational efficiency, and payer relationship management.
 <br/>
 <br/>
 Work Location:
 <br/>
 <br/>
 Qatar
 <br/>
 <br/>
 <strong>
  Industry
  <br/>
  <br/>
 </strong>
 Healthcare / Hospital
 <br/>
 <br/>
 <strong>
  Employment Type
  <br/>
  <br/>
 </strong>
 Full-Time
</div>


Insurance Manager

<div>
 DOC Medical Center is seeking an experienced Insurance Officer
 <br/>
 <br/>
 Approvals responsible for managing medical insurance approval processes, ensuring accurate and timely claims submission, and maintaining compliance with insurance policies and regulatory requirements. The role involves coordinating with insurance companies, healthcare providers, and patients to facilitate smooth approval workflows, minimize rejections, and ensure efficient reimbursement and claims processing across the organization.
 <br/>
 <br/>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 Educational Qualification: MBBS/BDS/B.Sc. Nursing/B. Pharm/Any allied healthcare qualification [Preferred] OR Bachelors Degree in Finance, Business Administration, Healthcare Management, or related field.
 <br/>
 <br/>
 Minimum 45 years of experience in medical insurance, approvals, or billing in Qatar.
 <br/>
 <br/>
 CPC (Certified Professional Coder) certification
 <br/>
 <br/>
 Mandatory.
 <br/>
 <br/>
 Strong knowledge of insurance policies, approval processes, medical coding, and billing systems.
 <br/>
 <br/>
 Good understanding of Qatar healthcare insurance procedures and MoPH regulations.
 <br/>
 <br/>
 Strong attention to detail, accuracy, and process compliance.
 <br/>
 <br/>
 Excellent communication and coordination skills.
 <br/>
 <br/>
 <strong>
  Key Responsibilities
  <br/>
  <br/>
 </strong>
 Process and submit insurance claims accurately and ensure timely approvals.
 <br/>
 <br/>
 Verify patient insurance eligibility, coverage, and pre-authorization requirements.
 <br/>
 <br/>
 Review claims for completeness, accuracy, and compliance prior to submission.
 <br/>
 <br/>
 Follow up on pending, rejected, and delayed approvals to ensure timely resolution.
 <br/>
 <br/>
 Coordinate with insurance companies on coverage, policies, and payment guidelines.
 <br/>
 <br/>
 Ensure billing and documentation align with insurance contracts and coding standards.
 <br/>
 <br/>
 Work with billing and revenue cycle teams to resolve claim discrepancies and improve reimbursements.
 <br/>
 <br/>
 Maintain accurate records and reports of approvals, claims, rejections, and reimbursements.
 <br/>
 <br/>
 Ensure compliance with Qatar MoPH regulations and insurance requirements.
 <br/>
 <br/>
 Analyze rejection trends and support process improvements to reduce claim denials.
 <br/>
 <br/>
 Work Location:
 <br/>
 <br/>
 Qatar
 <br/>
 <br/>
 <strong>
  Industry
  <br/>
  <br/>
 </strong>
 Healthcare / Hospital
 <br/>
 <br/>
 <strong>
  Employment Type
  <br/>
  <br/>
 </strong>
 Full-Time
</div>


Insurance Officer – Approvals

Shifamed LLC

<div><div><div>Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana&trade; Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing NavIQ&trade;, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&amp;D and manufacturing center in Doha, Qatar.</div>
<div></div><div>ABOUT SHIFAMED</div>
<div>Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.</div>
</div><div></div><p>Description:</p>
<p></p><p>This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&amp;D, and Executive Leadership to support U.S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands-on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.</p>
<p></p><p>Responsibilities, Skills &amp; Hands-On Experience:</p>
<p><br>
Regulatory Strategy &amp; Product Development:</p>
<ul><li>Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies.</li>
<li>Serve as regulatory lead on cross-functional product development teams from concept through commercialization.</li>
<li>Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes.</li>
<li>Partner with Quality and R&amp;D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements.</li>
</ul><p>FDA Regulatory Affairs</p>
<ul><li>Lead preparation, review, and submission of U.S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable.</li>
<li>Monitor evolving FDA requirements and assess impact on development and commercialization plans.</li>
</ul><p>International Regulatory Expansion</p>
<ul><li>Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets.</li>
<li>Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants.</li>
<li>Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries.</li>
<li>Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners.</li>
</ul><p>Clinical &amp; Regulatory Operations</p>
<ul><li>Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies.</li>
<li>Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways.</li>
<li>Support regulatory submissions associated with clinical trial approvals across multiple countries and regions.</li>
<li>Participate in investigator meetings, regulatory inspections, audits, and agency interactions.</li>
</ul><p>Agency Interactions &amp; Compliance</p>
<ul><li>Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities.</li>
<li>Support preparation for regulatory inspections and audits.</li>
<li>Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership.</li>
<li>Contribute to regulatory intelligence activities and long-term market expansion planning.</li>
</ul><p>Cross-Functional Leadership</p>
<ul><li>Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&amp;D teams to ensure regulatory requirements are incorporated throughout the product lifecycle.</li>
<li>Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities.</li>
<li>Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.</li>
</ul><p>Qualifications &amp; Experience:</p>
<ul><li>Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.</li>
<li>10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred.</li>
<li>Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements.</li>
<li>Experience supporting clinical-stage medical device programs and global clinical studies.</li>
<li>Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks.</li>
<li>Experience interacting directly with regulatory agencies, notified bodies, and international health authorities.</li>
<li>Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable.</li>
<li>Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development.</li>
<li>Excellent written, verbal, and presentation skills.</li>
<li>Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams.</li>
</ul><p>Preferred Qualifications:</p>
<ul><li>Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies.</li>
<li>Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets.</li>
<li>Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.</li>
</ul>
<div></div><div><div>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.</div>
<div></div><div>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.</div></div></div>

Manager / Sr. Manager, Regulatory Affairs

Shifamed

<div>
 Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana&trade; Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing NavIQ&trade;, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&amp;D and manufacturing center in Doha, Qatar.
 <br/>
 <br/>
 <strong>
  About Shifamed
  <br/>
  <br/>
 </strong>
 Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.
 <br/>
 <br/>
 Description:
 <br/>
 <br/>
 This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&amp;D, and Executive Leadership to support U.S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands-on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.
 <br/>
 <br/>
 Responsibilities, Skills &amp; Hands-On Experience:
 <br/>
 <br/>
 Regulatory Strategy &amp; Product Development:
 <br/>
 <br/>
 <ul>
  <li>
   Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies.
  </li>
  <li>
   Serve as regulatory lead on cross-functional product development teams from concept through commercialization.
  </li>
  <li>
   Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes.
  </li>
  <li>
   Partner with Quality and R&amp;D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 FDA Regulatory Affairs
 <br/>
 <br/>
 <ul>
  <li>
   Lead preparation, review, and submission of U.S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable.
  </li>
  <li>
   Monitor evolving FDA requirements and assess impact on development and commercialization plans.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 International Regulatory Expansion
 <br/>
 <br/>
 <ul>
  <li>
   Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets.
  </li>
  <li>
   Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants.
  </li>
  <li>
   Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries.
  </li>
  <li>
   Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Clinical &amp; Regulatory Operations
 <br/>
 <br/>
 <ul>
  <li>
   Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies.
  </li>
  <li>
   Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways.
  </li>
  <li>
   Support regulatory submissions associated with clinical trial approvals across multiple countries and regions.
  </li>
  <li>
   Participate in investigator meetings, regulatory inspections, audits, and agency interactions.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Agency Interactions &amp; Compliance
 <br/>
 <br/>
 <ul>
  <li>
   Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities.
  </li>
  <li>
   Support preparation for regulatory inspections and audits.
  </li>
  <li>
   Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership.
  </li>
  <li>
   Contribute to regulatory intelligence activities and long-term market expansion planning.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Cross-Functional Leadership
 <br/>
 <br/>
 <ul>
  <li>
   Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&amp;D teams to ensure regulatory requirements are incorporated throughout the product lifecycle.
  </li>
  <li>
   Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities.
  </li>
  <li>
   Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Qualifications &amp; Experience:
 <br/>
 <br/>
 <ul>
  <li>
   Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.
  </li>
  <li>
   10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred.
  </li>
  <li>
   Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements.
  </li>
  <li>
   Experience supporting clinical-stage medical device programs and global clinical studies.
  </li>
  <li>
   Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks.
  </li>
  <li>
   Experience interacting directly with regulatory agencies, notified bodies, and international health authorities.
  </li>
  <li>
   Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable.
  </li>
  <li>
   Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development.
  </li>
  <li>
   Excellent written, verbal, and presentation skills.
  </li>
  <li>
   Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Preferred Qualifications:
 <br/>
 <br/>
 <ul>
  <li>
   Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies.
  </li>
  <li>
   Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets.
  </li>
  <li>
   Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.
 <br/>
 <br/>
 NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
</div>


Oryx Veterinary Center

<div>
 <p>
  Oryx Veterinary Clinic is a modern and expanding veterinary center committed to delivering exceptional care to animals. We foster a collaborative, professional environment where passion for animal welfare meets clinical excellence.
 </p>
 <p>
  <strong>
   Job Summary
  </strong>
 </p>
 <p>
  <strong>
   We are seeking a highly experienced Veterinary Doctor to join our team. The ideal candidate will have strong clinical expertise, surgical skills, and the ability to manage a variety of cases, including small animals and exotic species.
  </strong>
 </p>
 <p>
  <strong>
   <u>
    Key Responsibilities
   </u>
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Diagnose and treat a wide range of medical conditions in animals
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Perform surgical procedures and oversee patient care before, during, and after surgery
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Handle emergency and critical care cases
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Develop treatment plans and ensure accurate medical records
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Provide clear communication and guidance to pet owners
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Supervise and support veterinary nurses and technicians
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Maintain high standards of hygiene, safety, and clinical excellence
  </strong>
 </p>
 <p>
  <strong>
   <u>
    Requirements
   </u>
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Minimum 5 years of advanced veterinary experience
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Qatar veterinary license preferred (or eligibility to obtain)
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong expertise in clinical diagnostics, surgery, and critical care
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent understanding in Ortho, skin, diet for the animals
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Experience with small animals and exotic species
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent communication and interpersonal skills
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong leadership and teamwork abilities
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to work in a fast-paced, dynamic environment
  </strong>
 </p>
 <p>
  <strong>
   <u>
    What We Offer
   </u>
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Professional and supportive work environment
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Opportunities for career growth and development
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Exposure to diverse and complex cases
  </strong>
 </p>
 <p>
  <strong>
   &middot;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Collaborative and passionate team culture
  </strong>
 </p>
 <p>
  <strong>
   <u>
    How to Apply
   </u>
  </strong>
 </p>
 <ul>
  <li>
   <strong>
    📩 Send your CV to hr@oryxvet.qa📞 Contact: +974 6000 5057
   </strong>
  </li>
 </ul>
</div>


Veterinary Doctor

Apex Health 

<p><b>Job Summary</b></p><p>The Emergency Room Nurse is responsible for providing rapid assessment, planning, implementation, and evaluation of nursing care for patients presenting with acute illnesses, injuries, and life-threatening conditions. The role requires the ability to prioritize care, respond effectively to emergencies, collaborate with multidisciplinary teams, and deliver high-quality, patient-centered care in a fast-paced environment.</p><p><b>Key Responsibilities</b></p><p><b>Clinical Care</b></p><ul><li>Perform rapid patient assessments and triage according to established emergency department protocols.</li><li>Identify actual and potential health problems and prioritize care based on patient acuity.</li><li>Initiate emergency nursing interventions and provide immediate care for critically ill or injured patients.</li><li>Monitor, assess, and document patients' clinical conditions and responses to treatment.</li><li>Administer medications, intravenous therapies, blood products, and treatments as prescribed.</li><li>Assist physicians and other healthcare professionals during examinations, procedures, and resuscitation efforts.</li><li>Operate and monitor emergency equipment, including cardiac monitors, defibrillators, ventilators, and infusion devices.</li><li>Respond promptly to medical emergencies, trauma cases, cardiac arrests, and disaster situations.</li></ul><p><b>Patient and Family Care</b></p><ul><li>Provide compassionate care and emotional support to patients and families during emergency situations.</li><li>Educate patients and families regarding treatment plans, discharge instructions, medications, and follow-up care.</li><li>Advocate for patient safety, dignity, and rights throughout the care process.</li><li>Facilitate effective communication between patients, families, and the healthcare team.</li></ul><p><b>Care Coordination</b></p><ul><li>Collaborate with physicians, paramedics, respiratory therapists, laboratory personnel, radiology staff, and other healthcare professionals.</li><li>Coordinate admissions, transfers, referrals, and discharges as appropriate.</li><li>Ensure continuity of care through effective handovers and documentation.</li></ul><p><b>Quality and Patient Safety</b></p><ul><li>Adhere to infection prevention and control standards.</li><li>Ensure compliance with emergency department policies, procedures, and regulatory requirements.</li><li>Participate in quality improvement, risk management, and patient safety initiatives.</li><li>Report and document incidents, adverse events, and safety concerns according to organizational policy.</li><li>Support disaster preparedness and emergency response planning activities.</li></ul><p><b>Documentation</b></p><ul><li>Maintain accurate, timely, and complete patient records in the electronic medical record system.</li><li>Document assessments, interventions, treatments, medications, and patient outcomes in accordance with professional standards.</li></ul><p><b>Professional Practice</b></p><ul><li>Maintain clinical competency in emergency nursing practices and procedures.</li><li>Participate in continuing education, mandatory training, and professional development activities.</li><li>Serve as a resource and mentor to junior nursing staff when appropriate.</li><li>Participate in departmental meetings, audits, accreditation activities, and performance improvement initiatives.</li></ul><p><b>Qualifications</b></p><ul><li>Bachelor's Degree in Nursing or equivalent recognized nursing qualification.</li><li>Current Registered Nurse license in accordance with local regulatory requirements.</li></ul><p><b>Certifications</b></p><ul><li>Basic Life Support (BLS) &ndash; Required.</li><li>Advanced Cardiac Life Support (ACLS) &ndash; Required.</li><li>Pediatric Advanced Life Support (PALS) &ndash; Preferred/Required based on department scope.</li><li>Trauma Nursing Core Course (TNCC) or equivalent trauma certification &ndash; Preferred.</li></ul><p><b>Experience</b></p><ul><li>Minimum 4 years of clinical nursing experience.</li><li>Previous experience in Emergency Department, Critical Care, Intensive Care Unit (ICU), Trauma, or Acute Care settings preferred.</li></ul><p><b>Skills and Competencies</b></p><ul><li>Strong emergency assessment and triage skills.</li><li>Ability to perform effectively under pressure and in rapidly changing situations.</li><li>Excellent critical thinking and clinical decision-making abilities.</li><li>Strong communication and interpersonal skills.</li><li>Ability to prioritize workload and manage multiple patients simultaneously.</li><li>Proficiency in emergency equipment and clinical technologies.</li><li>Commitment to patient safety, quality care, and professional practice.</li></ul><p>Education:</p><ul><li>Bachelor's (Preferred)</li></ul><p>Experience:</p><ul><li>Emergency Nurse : 4 years (Required)</li></ul><p>Work Location: In person</p>

Emergency Room Nurse

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