Doctor Jobs

Role & Responsibilities • Perform end-to-end ICSR case processing for marketed products in compliance with global regulations • Assess seriousness, expectedness, causality, and ensure accurate global reporting • Process literature ICSRs and maintain monitoring compliance • Support aggregate reporting activities including PSURs and DSURs • Maintain pharmacovigilance database integrity (LSMV experience preferred) • Conduct reconciliation activities and support KPI/SLA tracking • Collaborate with medical, clinical, and cross-functional teams on safety evaluations • Identify safety trends and support signal detection and risk management • Participate in regulatory audits and inspections • Train and mentor junior pharmacovigilance associates • Review SOPs and contribute to continuous PV process improvement Qualification • B.Pharm / M.Pharm / Pharm.D / BDS / B.Sc Nursing / M.Sc Nursing / BAMS / BHMS Experience • 4+ years of pharmacovigilance case processing experience • Experience in Post-Marketing Surveillance (PMS) • Strong knowledge of global pharmacovigilance regulations • Hands-on experience with safety databases (LSMV preferred) • Familiarity with SDEA concepts and SLA/KPI management Skills • Pharmacovigilance & Drug Safety Operations • ICSR Processing (Marketed Products) • Aggregate Reports (PSUR / DSUR) • Global Safety Reporting • Signal Detection (supporting role) • Audit & Inspection Readiness • Excellent analytical and communication skills • Proficiency in Microsoft OfficeBenefits • Competitive salary & performance-based rewards • Multiple annual leave entitlements • Comprehensive health insurance for employee & family • Retirement & long-term savings plans • Global Employee Assistance Program (TELUS Health) – 24/7 support • Life assurance coverage • Flexible benefits (childcare support, gym discounts, travel subsidies, wellness programs) • Inclusive, diverse, and harassment-free workplace About The Company • ICON Plc – A global leader in healthcare intelligence and clinical research, ICON provides comprehensive solutions across the clinical trial process. With a strong commitment to regulatory compliance and patient safety, ICON offers career advancement opportunities for professionals in pharmacovigilance and drug safety.

Role & Responsibilities • Process and triage Individual Case Safety Reports (ICSRs) • Ensure data accuracy, completeness, and regulatory compliance in safety reporting • Perform medical coding of adverse events, medical history, and medications using MedDRA • Support xEVMPD submissions and SPOR/IDMP activities • Maintain documentation within TMF and Pharmacovigilance system master files • Collaborate with global safety teams to meet regulatory timelines Qualification • Degree in Pharmacy, Life Sciences, or related healthcare discipline (e.g., B.Pharm, M.Pharm, Pharm.D, MSc, BDS) Experience • 2.6 to 4.5 years of hands-on experience in ICSR case processing • Proven experience with Argus, ArisG, or LSMV safety databases • Strong understanding of global pharmacovigilance regulations • Knowledge of MedDRA coding and safety reporting workflows Skills • Expertise in pharmacovigilance and safety reporting • Ability to manage and maintain accurate documentation • Strong collaboration and communication skills in a global setting About The Company • Syneos Health – A global biopharmaceutical solutions organization, Syneos Health provides a full spectrum of clinical, medical affairs, and commercialization services. The company is committed to delivering innovative solutions across the drug development lifecycle, from preclinical to post-marketing. Syneos Health fosters a collaborative work culture with global exposure and career growth opportunities.

Role & Responsibilities • Exchange and disseminate scientific, educational, and research-related information with Thought Leaders (TLs) proactively and reactively • Provide clarification and education of scientific data, study protocols, meeting abstracts, and professional literature, both on-label and off-label, in alignment with local regulations • Answer medical/scientific queries from Medical Societies regarding Bayer products • Organize, support, and participate in advisory boards • Attend congresses and conventions, interact with TLs, establish new contacts, and gather competitive intelligence • Plan and organize scientific education and training events with TLs within specific therapeutic areas or products • Contribute to internal understanding of specific TL interests and expertise within the medical community • Submit timely reports and track activities against agreed objectives • Provide external scientific support, training, and education where needed Qualification • Qualification in natural sciences or a medical background (MD, MBBS, BAMS, BDS, MDS) Experience • Basic knowledge of the concerned therapy area and related molecules • Basic understanding of clinical trials, their design, and rationale • Experience working independently and within a team environment • Ability to build productive relationships both internally and externally Skills • Excellent presentation and written and verbal communication skills • Ability to engage and influence thought leaders and stakeholders effectively • Proficiency in managing scientific data and presenting it clearly to diverse audiences About The Company • Bayer – A global leader in life sciences, Bayer is dedicated to driving innovation and improving lives through advanced solutions in healthcare and agriculture. The company values dynamic shared ownership (DSO) and fosters a work environment that prioritizes higher productivity, faster innovation, and better results. Bayer is committed to diversity and inclusivity, promoting fairness and respect at work.

Role & Responsibilities • Develop and maintain professional relationships with internal and external customers to provide medical and scientific support for AbbVie initiatives in oncology • Execute the Medical Affairs plan for India and provide scientific education and training across AbbVie’s oncology portfolio • Lead scientific communication with key therapy leaders and stakeholders, organizing advisory boards, facilitating clinical trials, and serving as a medical resource • Provide fair and balanced scientific information to healthcare professionals (HCPs) on AbbVie products • Facilitate educational and research activities for physicians and healthcare professionals regarding current and future AbbVie therapies • Collaborate with commercial teams to ensure the information and training needs of healthcare professionals are met • Present AbbVie product data to healthcare professionals, academic institutions, and researchers • Support research initiatives requested by AbbVie R&D, Clinical Operations, and Medical Affairs departments • Serve as an internal medical and scientific resource for developing disease-state and product communications • Support Round Table and Advisory Board sessions to ensure scientific and clinical data accuracy • Conduct ongoing training for medical affairs, field sales, and internal teams • Travel approximately 60% of the time for field-based activities Qualification • MD or MBBS (Medical degree) Experience • 2-3 years of post-qualification experience in Medical Affairs • Experience in the pharmaceutical industry or clinical research preferred • Experience working collaboratively in a cross-functional matrix structure • Demonstrated ability to convey technical information to individuals with varying degrees of scientific knowledge • Strong presentation and teaching skills • Ability to build and maintain strong relationships with healthcare professionals and stakeholders Skills • Strong analytical skills to evaluate and communicate key clinical data • Proficiency in Microsoft Office and other relevant technology systems • Ability to engage and influence thought leaders and internal teams About The Company • AbbVie – A global biopharmaceutical company dedicated to improving lives through innovative medicines and solutions. AbbVie operates across key therapeutic areas such as immunology, oncology, neuroscience, and eye care, with a strong commitment to research and patient care. The company values diversity and inclusivity, fostering a collaborative and innovative environment to address the medical challenges of today and tomorrow.

Role & Responsibilities • Lead medical affairs objectives in the assigned country, serving as an internal medical, technical, and scientific resource • Use medical and scientific information to facilitate physician engagement on clinical and scientific issues relevant to AbbVie’s products • Identify and develop professional relationships with thought leaders, academic centers, and researchers in assigned therapeutic areas • Work closely with commercial leaders and medical affairs teams to set priorities and define strategies • Present AbbVie product data to healthcare professionals, academic institutions, and researchers upon request • Support research initiatives, collaborating with AbbVie R&D, Clinical Operations, and Medical Affairs departments • Develop scientifically accurate, balanced, and compliant disease-state and product communications • Support Round Table and Advisory Board sessions to ensure the accuracy of clinical data • Conduct ongoing training for internal teams, including medical affairs and field sales • Travel approximately 60% of the time for field-based activities, serving as the local representative of the Global Medical Office Qualification • MD, MBBS, or Pharm D Experience • 2-3 years of post-qualification experience in the Medical Affairs function • Experience within the pharmaceutical industry or clinical research is preferred • Ability to work cross-functionally in a matrix structure and support multiple stakeholders • Strong presentation and teaching skills to convey technical information effectively • Demonstrated ability to develop and maintain strong relationships with key stakeholders • Experience in evaluating and communicating clinical data effectively Skills • Ability to convey complex scientific and clinical data to individuals with varying scientific knowledge • Strong analytical and problem-solving skills • Proficiency with technology and systems like Microsoft Office About The Company • AbbVie – A global leader in the pharmaceutical industry, AbbVie is committed to delivering innovative medicines that solve serious health issues today and address tomorrow’s challenges. The company is deeply involved in multiple therapeutic areas including immunology, oncology, neuroscience, and eye care, with a commitment to improving lives through advanced treatments and solutions.

Role & Responsibilities • Execute the Medical Affairs strategy for AbbVie’s oncology portfolio in India • Provide scientific education and training initiatives across AbbVie’s oncology portfolio • Engage proactively and reactively with healthcare professionals (HCPs), disseminating scientific, educational, and research-related information • Serve as the primary contact for medical and scientific inquiries related to AbbVie products • Organize and participate in advisory boards, congresses, and conventions, interacting with Thought Leaders (TLs) • Support clinical trials and research initiatives, providing scientific support to AbbVie R&D, Clinical Operations, and Medical Affairs • Maintain professional relationships with key opinion leaders (KOLs), academic institutions, and researchers • Facilitate the development and distribution of scientifically accurate, balanced, and regulatory-compliant product communications and materials • Provide field-based medical support for HCPs and contribute to the development of disease-state communications • Participate in the training of medical affairs, field sales, and internal teams on scientific and product knowledge • Travel approximately 60% of the time for field-based activities Qualification • MD or MBBS (Medical Degree) • Post-qualification experience in Medical Affairs or clinical research, preferably in oncology Experience • 2-3 years of experience in the Medical Affairs function or clinical research • Experience in the pharmaceutical industry or related clinical research settings is preferred • Strong presentation and teaching skills with the ability to effectively communicate clinical and non-clinical data • Ability to build and maintain relationships with internal and external stakeholders • Experience in scientific training, product management, and clinical communication Skills • Strong knowledge of oncology therapeutics and clinical trial processes • Ability to critically evaluate and effectively communicate key clinical data • Experience with MS Office applications and other technological systems • Excellent interpersonal and communication skills • Ability to work independently and within a team, managing multiple stakeholders About The Company • AbbVie – A global biopharmaceutical company focused on discovering and delivering innovative medicines that address serious health challenges, including oncology, immunology, neuroscience, and eye care. AbbVie is dedicated to transforming patients' lives with cutting-edge therapies and solutions in collaboration with healthcare professionals and researchers worldwide.

Role & Responsibilities • Engage proactively and reactively with Thought Leaders (TLs), providing scientific, educational, and research-related information on Bayer products • Disseminate and clarify scientific data, study protocols, meeting abstracts, and professional literature • Participate in clinical trial activities, including company-sponsored and investigator-initiated research • Answer medical/scientific queries from medical societies regarding Bayer products • Organize and support advisory boards and interactions with medical societies • Attend congresses and conventions to network with TLs, gather competitive intelligence, and establish new contacts • Plan and organize scientific training and educational events with TLs in specific therapeutic areas or product lines • Identify, profile, and engage TLs, contributing to the internal understanding of their interests and expertise • Prepare and submit reports, tracking activities against agreed objectives Qualification • MD, MBBS, BDS, MDS, or equivalent in medical or dental education Experience • Basic knowledge of stroke and neurology therapy areas and related molecules • Basic understanding of clinical trials, their design, and rationale • Experience working independently and in team environments, building productive relationships with thought leaders Skills • Excellent presentation, written, and verbal communication skills • Ability to engage with and educate internal and external stakeholders on scientific topics • Strong organizational skills to plan and execute educational activities About The Company • Bayer Zydus Pharma – A leading global healthcare and pharmaceutical company committed to improving lives through innovative therapies. Bayer Zydus Pharma focuses on research-driven solutions in multiple therapeutic areas, including cardiovascular, neurology, and other high-impact medical fields.

Role & Responsibilities • Execute medical affairs strategy in the assigned zone, with a focus on relevant therapeutic areas • Understand current practices, medicines in use, and trends by engaging with key customer contacts, attending scientific symposia, and reviewing therapeutic journals • Provide clear, non-promotional communication to internal and external customers, positioning BI Medical as a preferred partner • Execute key medical projects (e.g., IIS studies) to ensure efficient interaction with customers and key customer networks • Participate in the implementation of the local medico-marketing strategy • Identify and build relationships with key stakeholders (EEs) in the territory to promote BI products effectively • Provide medical and product expertise towards product registrations and new indications, working closely with regulatory authorities • Assist with the defense of marketed products and provide expertise to regulators, NGOs, and the press • Write, revise, and review labeling documents for pipeline and local products as per relevant SOPs • Assist regulatory affairs with EE access when appropriate Qualification • Medical degree (preferably in Pharmacology) or qualification in Life Sciences • MD in Pharmacology is preferred for candidates without doctoral qualifications • For professionals without a doctoral qualification, relevant field-based work experience of 10+ years with strong scientific expertise is also acceptable Experience • 0-3 years of experience in the pharmaceutical or healthcare industry • Scientific expertise in the diabetes therapy area is required Skills • Excellent interpersonal skills and the ability to build strong relationships • Basic IT knowledge, including proficiency with MS Office applications • Ability to communicate scientific information clearly and effectively About The Company • Boehringer Ingelheim Group – A global leader in the pharmaceutical industry, dedicated to improving patient outcomes through innovative therapies and products. The company provides comprehensive solutions in multiple therapeutic areas, including diabetes, oncology, and immunology, with a focus on scientific excellence and customer collaboration.

Role & Responsibilities • Focus on Myopia Management as a new category for Essilor, providing expertise on myopia-related products • Speak knowledgeably about the myopia category to Ophthalmologists, Optometrists, and Opticians • Train and support ECP (Eye Care Professionals) staff on myopia management products • Open doors and promote sales for new myopia products • Conduct regular training sessions for ECPs, Optometrists, Ophthalmologists, and their staff • Troubleshoot and support selling efforts through education and engagement • Drive sales volume and value for myopia management products in the India business unit • Collaborate with business and sales teams to enhance product visibility and adoption Qualification • Bachelor’s degree in Optometry, Medicine, or related field • Postgraduate qualification in Management (preferred) Experience • At least 5 years of experience in Optometry, specifically related to PAL (Progressive Addition Lenses) or EPS (Eye Perception Services) • Experience in marketing, product management, or training related to medical devices or FMCG • Experience in the India market is essential; APAC experience is a plus • Confidence to train others and influence key stakeholders Skills • Strong ability to train and influence others • Goal-driven and result-oriented with clear, fact-based decision-making skills • Ability to work in a collaborative, cross-functional environment • Strong communication skills in English; proficiency in local languages is a plus • Multilingual skills are advantageous About The Company • EssilorLuxottica – A global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. The company offers a wide range of high-quality vision care products, including renowned brands such as Ray-Ban, Oakley, Persol, and Vogue Eyewear, along with a network of retailers like Sunglass Hut and LensCrafters.

Role & Responsibilities • Serve as a key representative of the Medical Affairs function, providing scientific and clinical expertise on Bioscan Research's technologies and innovations • Communicate complex medical and scientific information to healthcare professionals (HCPs) in a clear, accurate, and compliant manner • Establish and maintain strong relationships with key opinion leaders (KOLs), healthcare professionals, and other stakeholders in the field of traumatic brain injury • Collaborate with cross-functional teams to support clinical development, regulatory activities, and marketing efforts • Provide training and support to internal teams on the scientific and clinical aspects of the company's products • Monitor and report on trends in the field of traumatic brain injury and related medical advancements Qualification • Advanced degree in a relevant scientific or medical field (MD, PhD, or equivalent) Experience • Prior experience as a Medical Science Liaison or similar role in the pharmaceutical, biotechnology, or medical device industry • Experience in communicating scientific data to healthcare professionals • Knowledge in the area of traumatic brain injury or related fields Skills • Strong scientific and clinical knowledge, particularly in traumatic brain injury and neurotechnology • Excellent communication and interpersonal skills to engage with HCPs and KOLs • Ability to present complex scientific concepts in a clear and compliant manner • Strong problem-solving and critical thinking skills • Ability to work independently and collaboratively in a cross-functional environment About The Company • Bioscan Research – A company dedicated to improving traumatic brain injury patient outcomes through innovative technologies, including the machine learning-powered NIRS device, CEREBO, which aims to advance clinical understanding and treatment strategies for brain injury.

Role & Responsibilities • Provide specialized medical care in the designated field • Conduct consultations and provide diagnoses and treatment plans • Participate in ongoing patient care, ensuring effective management of medical conditions • Collaborate with healthcare teams to ensure patient well-being • Maintain accurate patient records in accordance with hospital policies Qualification • MBBS, MD/MS, DND, or Diploma in the relevant medical specialty Experience • Relevant experience in the specialty (specific experience requirements may vary based on the specialty) Skills • Strong clinical knowledge in the relevant specialty • Excellent diagnostic and patient-care skills • Ability to collaborate with medical teams for comprehensive patient care Age Limit • Minimum Age: 21 years • Maximum Age: 62 years Salary • Minimum Salary: Rs. 60,000/- per month Selection Process • Interview Application Fee • No application fee• Walk-in Interview Date: 05-02-2026Official NotificationClick Here

Role & Responsibilities • Provide comprehensive medical care to patients in a family medical practice • Diagnose, treat, and manage a wide range of health conditions • Conduct patient consultations and follow-up appointments • Offer telehealth consultations (work from home one day a week) • Collaborate with reception staff and allied health workers (e.g., speech pathology) • Maintain accurate patient records and documentation • Adhere to medical protocols and ensure patient safety and satisfaction Qualification • Vocationally Registered General Practitioner (VR GP) • Registration with the Australian Health Practitioner Regulation Agency (AHPRA) Experience • Experience as a VR General Practitioner Skills • Strong diagnostic and patient-care skills • Ability to provide telehealth services • Excellent communication and interpersonal skills • Ability to work independently and as part of a multidisciplinary team About The Company • Minchinbury Health Services – An established family medical practice in a close-knit, caring community suburb in Western Sydney, offering full-time and part-time opportunities with great work-life balance

Role & Responsibilities • Provide medical care and treatment to patients according to established protocols • Diagnose, treat, and manage a variety of medical conditions • Provide consultation to patients and collaborate with healthcare teams • Maintain accurate and up-to-date patient records • Participate in medical rounds and contribute to ongoing medical research • Stay current with advancements in medicine and treatment protocols Qualification • MBBS (Medicine) • Internship • MD/MS or equivalentVacancies - 10 Experience • Consultant: 12 years of experience in the specialty • Specialist: 3 years of experience in the specialty Skills • Strong clinical knowledge and diagnostic skills • Excellent communication and patient-care abilities • Ability to work effectively in a multidisciplinary team • Proficiency in maintaining patient records and documentation About The Company • Resolve – A healthcare provider in Saudi Arabia offering multiple doctor vacancies with competitive compensation packages, including housing, transportation, flight tickets, and schooling for children

Role & Responsibilities • Perform surgical procedures to remove tumors and other cancerous tissues • Collaborate with a multidisciplinary team to develop comprehensive treatment plans • Provide preoperative and postoperative care to patients • Conduct patient consultations and follow-up appointments • Stay current with advancements in oncology and surgical techniques • Participate in clinical research and trials • Educate and train medical students and residents • Maintain detailed and accurate patient records • Ensure compliance with medical protocols and standards • Provide compassionate and patient-centered care • Communicate effectively with patients and their families • Manage and mitigate surgical risks and complications • Participate in tumor board meetings and case discussions • Develop and implement quality improvement initiatives • Advocate for patient needs and preferences • Contribute to the development of clinical guidelines and protocols • Engage in continuous professional development and education Qualification • Specialization degree or Board certification in surgical oncology • Medical degree (MBBS, MS, or equivalent) from an accredited institution • Valid medical license to practiceVacancies no - 3 Experience • 5 - 10 years of extensive experience in surgical oncology • Proven track record of successful surgical outcomes • Experience in clinical research and trials • Teaching and mentoring experience Skills • Strong knowledge of oncology and cancer treatment protocols • Excellent surgical skills and precision • Strong communication and interpersonal skills • Empathy and compassion for patients • Ability to work effectively in a multidisciplinary team • Proficiency in electronic medical records (EMR) systems • Strong organizational and time-management skills • Ability to stay current with medical advancements • Strong problem-solving and decision-making skills About The Company • Client of Health7Careers – A leading healthcare employer offering opportunities for surgical oncologists in Dubai, UAE

Role & Responsibilities • Deliver high-quality, evidence-based, and patient-centered care in Dermatology • Support and adhere to all hospital departmental and divisional initiatives, policies, and procedures • Participate in the organization’s performance management system, including peer review and productivity and utilization review processes • Assist Consultant staff in ensuring adequate medical coverage within the Division • Attend Divisional meetings as invited and contribute to clinical discussions • Report, investigate, and respond to untoward incidents • Diagnose and treat patients according to established best practices for dermatology • Supervise and guide junior medical staff in their clinical duties • Lead ward rounds, reassess inpatients and outpatients regularly in line with best practices • Document clinical information clearly and promptly in accordance with hospital procedures • Review investigation results and modify treatment as necessary • Liaise with other medical specialties and support services for additional input • Actively participate in multi-disciplinary meetings to plan holistic care for patients Qualification • MBBS (Medicine) • Tier 1, Tier 2, or Tier 3 qualifications depending on experience Experience • Tier 1: No additional experience required post-board certification • Tier 2: Minimum 2 years of clinical experience post-qualification in an internationally accredited institute • Tier 3: Minimum 3 years of clinical experience post-qualification as a Specialist in an internationally accredited institute • UAE Nationals: No additional experience required post-board certification Skills • Strong clinical knowledge and skills in Dermatology • Ability to supervise junior medical staff and work in a multi-disciplinary team • Effective communication and documentation skills • Commitment to patient-centered care About The Company • Sheikh Shakhbout Medical City – A leading medical institution in Abu Dhabi, providing top-tier healthcare services

Role & Responsibilities • Conduct telehealth consultations with patients seeking alternative medicine treatment • Assess patient suitability based on medical history, current conditions, and prior treatments • Prescribe medicinal cannabis where clinically appropriate and in line with TGA requirements • Develop individualized treatment plans focused on safety, function, and quality of life • Provide follow-up consultations and ongoing monitoring • Educate patients on expected benefits, dosing, and responsible use • Maintain accurate and thorough clinical records • Practice in accordance with AHPRA standards and relevant state and federal regulations • Ensure informed consent is obtained and documented • Identify and report adverse events in line with pharmacovigilance obligations • Work collaboratively with the nursing team and clinical management Qualification • Current unrestricted registration with AHPRA • Eligibility to prescribe Schedule 8 medications • TGA Authorised Prescriber status for Medicinal Cannabis Categories 1-5 Experience • Experience managing chronic conditions such as pain or mental health presentations • Understanding of Australia’s medicinal cannabis regulatory environment • Telehealth consultation experience (desirable but not essential) Skills • Strong communication skills and a patient-focused approach • Interest in cannabinoid medicine and emerging treatment options • Ability to work independently in a telehealth model About The Company • Healing Leaves Clinic – A patient-focused telehealth clinic offering alternative medicine care, including medicinal cannabis, for patients with complex health conditions.

Role & Responsibilities • Provide comprehensive general medical care to patients in a busy, dynamic clinic • Work in a supportive and friendly environment, ensuring high-quality patient care • Collaborate with a team of healthcare professionals to deliver best practices • Offer treatment, advice, and referrals based on patients' medical needs • Manage patient records and documentation in line with clinic protocols Qualification • Fellowship with the Royal Australian College of General Practitioners (RACGP) Experience • Experience as a General Practitioner • Relevant experience in a family clinic or similar healthcare setting Skills • Strong communication skills for patient care and collaboration • Ability to manage diverse medical conditions • Ability to work effectively in a team environment About The Company • Emma Court Family Clinic – A busy, dynamic clinic in Woori Yallock, VIC, offering high salary opportunities in a supportive and friendly work environment

Role & Responsibilities • Provide telehealth consultations for common medical issues, such as prescription requests, pathology referrals, medical certificates, and general medical advice • Work remotely using a purpose-built telehealth platform • Offer empathetic and effective communication to ensure high-quality care for patients • Work independently while receiving robust admin and clinical support • Follow medical board telehealth guidelines and provide excellent care • Flexible hours, with the ability to start at 3-4 hours/week or more Qualification • General AHPRA Registration (unrestricted) • Fellowship of RACGP/ACRRM (preferred but not required) Experience • Experience in general medical practice • Ability to work independently in a telehealth setting Skills • Empathetic & effective communication skills • Ability to manage medical consultations remotely and provide accurate advice • Familiarity with telehealth systems and private billing About The Company • Qoctor – A doctor-led telehealth platform that provides quality healthcare services remotely, with flexible hours and competitive pay.

Role & Responsibilities • Perform and interpret diagnostic imaging studies including X-ray, CT, MRI, Ultrasound, and other modalities as applicable • Provide accurate and timely radiology reports to support clinical decision-making • Collaborate with physicians and clinical teams to ensure optimal patient care • Maintain proper documentation in line with DOH and hospital policies • Ensure radiation safety standards and quality control procedures are followed • Participate in audits, quality improvement initiatives, and departmental meetings Qualification • MBBS/MD or equivalent with specialization in Radiology Experience • 7 - 9 years of post-specialization experience in radiology (as per DOH criteria) • Experience in hospital or advanced diagnostic center settings • Sub-specialty experience (CT/MRI/Interventional, if applicable) Skills • Strong knowledge of diagnostic imaging protocols • Excellent communication and reporting skills • Ability to work independently and as part of a multidisciplinary team • Familiarity with PACS/RIS systems About The Company • Royal Health Group AE – A leading healthcare provider in the UAE