Doctor Jobs

Role & Responsibilities • Conduct review and assessment of individual case safety reports (ICSRs) obtained from clinical trials, spontaneous, and solicited reports • Determine regulatory reportability of cases within assigned therapeutic teams and across all products/sites in a timely manner • Perform triage of cases and assess seriousness and relatedness across products • Review and verify appropriate selection of adverse events from source documents, assign MedDRA codes, assess labeling, and review narratives • Maintain current knowledge of product portfolio and safety profiles across therapeutic areas • Escalate complex case issues to the medical review team of the client as necessary • Conduct assessment of litigation cases across products • Identify and resolve case issues, and coordinate with client therapeutic teams or functional groups • Communicate effectively within and across all client therapeutic teams, and within functional management • Maintain knowledge of applicable Global Health Authority regulations • Perform additional drug safety-related activities as assigned Qualification • MBBS or MD • Mandatory: MCI Registration/State Medical Council Registration Experience • 1 - 3 years in Pharmacovigilance or related medical review experience Skills • Experience with relevant safety databases and related software applications • Proven customer handling and relationship management skills • Strong task management and ability to deliver within established timelines • Excellent presentation and communication skills, both verbal and written • Knowledge of the Life Sciences industry and the drug development lifecycle • Familiarity with medical and therapeutic terminology • Understanding of Patient Safety regulatory obligations • High attention to detail About The Company • Qinecsa Solutions – A leading provider of pharmacovigilance and drug safety services, specializing in the evaluation and management of drug safety for pharmaceutical companies globally.

Role & Responsibilities • Conduct review and assessment of individual case safety reports (ICSRs) obtained from clinical trials, spontaneous, and solicited reports • Determine regulatory reportability of cases within assigned therapeutic teams and across all products/sites • Perform triage of cases and assess seriousness and relatedness across products • Review and verify appropriate selection of adverse events from source documents, assign appropriate MedDRA codes, and assess labeling • Review and write narratives for ICSR • Acquire and maintain current knowledge of product portfolio and safety profiles across therapeutic areas • Escalate complex case issues to the medical review team of the client as needed • Conduct assessment of litigation cases across products as assigned • Identify and resolve case issues, coordinating with client therapeutic teams and functional groups • Communicate effectively within and across client therapeutic teams and functional management • Maintain knowledge of applicable Global Health Authority regulations and drug safety standards • Perform other drug safety related activities as assigned Qualification • MBBS or MD • Mandatory: MCI Registration/State Medical Council Registration Experience • 1 - 3 years of relevant experience in Pharmacovigilance, specifically as a Medical Reviewer Skills • Experience with relevant safety databases and related software applications • Proven customer handling and relationship management skills • Task management and ability to deliver within established timelines • Strong presentation skills with the ability to deliver clear and engaging presentations • Knowledge of the Life Sciences Industry and lifecycle of drug development • Strong competence in medical and therapeutic terminology • Understanding of Patient Safety regulatory obligations • High attention to detail • Proficiency in spoken and written English with excellent comprehension About The Company • Qinecsa Solutions – A leading provider of pharmacovigilance and drug safety services. Qinecsa Solutions specializes in offering comprehensive drug safety and medical review services for global pharmaceutical companies.

Role & Responsibilities • Provide medical review, analysis, and guidance during the case handling and reporting cycle of Adverse Event (AE) and Adverse Reaction reports for investigational and marketed products • Conduct signal detection, analysis, evaluation, and ongoing safety surveillance activities • Provide medical guidance and input to Drug Safety Associates (DSAs) and specialists in the medical aspects of drug safety • Act as a pharmacovigilance representative and safety scientist • Maintain a good working knowledge of the Adverse Event profile of assigned products, labeling documents, data handling conventions, client’s guidelines, and international drug safety regulations • Ensure compliance with internal and regulatory timelines for adverse event reporting • Communicate and discuss issues related to the review process with the Project Manager • Interact with internal and external contacts to resolve issues • Attend and present client/cross-functional meetings with other stakeholders Case Report Medical Review • Perform medical review of cases according to client Standard Operating Procedures (SOPs) • Write Pharmacovigilance/Marketing Authorization Holder (MAH) comments and assess company causality • Assess seriousness and expectedness of reported events • Provide medical advice to the case processing team Qualification • MBBS or MD (Medical Doctor) Experience • Fresher or relevant experience in pharmacovigilance/Drug Safety is preferred Skills • Excellent interpersonal, verbal, and written communication skills • Client-focused approach to work • Flexible attitude with respect to work assignments and new learnings • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail • Strong knowledge of international drug regulations, including GCP (Good Clinical Practice) and GVP (Good Pharmacovigilance Practice) • Ability to assess the clinical relevance of medical data and interpret its clinical meaning About The Company • Parexel – A leading global provider of biopharmaceutical services, Parexel specializes in drug development and regulatory consulting. With a focus on high-quality services and innovative healthcare solutions, Parexel works with clients to ensure the safety and efficacy of drugs across the clinical development lifecycle.

Role & Responsibilities • Perform medical review and assessment of individual case reports of adverse events (AEs) and other safety information related to Sanofi products • Review and evaluate medical information from case reports, determining the causality assessment • Prepare detailed and thorough safety narratives • Participate in the medical evaluation of safety signals, risk management planning, and benefit-risk assessment • Respond to medical information requests from healthcare providers, patients, and regulatory authorities • Provide medical expertise and input to cross-functional teams, including regulatory affairs and clinical teams Qualification • Medical degree (MBBS, MD, or equivalent) • 3+ years of experience in pharmacovigilance, drug safety, or a related field Experience • Proven experience in reviewing adverse events, causality assessment, and preparing safety narratives • Familiarity with safety signal management and risk management strategies • Experience working with cross-functional teams in a pharmaceutical or biopharmaceutical company Skills • Medical review and evaluation of adverse events • Causality assessment and benefit-risk assessment • Strong understanding of safety information processing and reporting • Ability to respond to medical information requests and provide expertise to healthcare providers • Excellent communication and collaboration skills About The Company • Sanofi – A global biopharmaceutical company focused on human health. Sanofi is dedicated to discovering, developing, and distributing therapeutic solutions to improve the lives of people facing serious illnesses.

Role & Responsibilities • Prepare and quality-check aggregate reports such as Periodic Benefit Risk Evaluation Reports (PBRERs), Periodic Safety Update Reports (PSURs), and US Periodic Adverse Drug Experience Reports (PADERs) from aggregate data • Conduct signal detection-related analyses, including cumulative analyses, issue event analyses, and Signal Evaluation Reports • Review published literature and case listings, ensuring vigilance over important/designated medical events • Interact with client personnel to discuss potential signals and issues detected with products • Support the preparation and maintenance of Risk Management Plans (RMPs) • Follow-up with clients to obtain missing or incomplete information to resolve and clarify issues • Perform medical review of individual case safety reports (ICSRs) and narratives for Clinical Study Reports (CSRs) • Provide medical advice to drug safety scientists on the processing of ICSRs and CSR narratives • Maintain knowledge of the adverse event safety profile of assigned drugs, labelling documents, and client guidelines • Ensure compliance with global regulatory reporting obligations and internal timelines for report submissions • Maintain records in compliance with guidelines and Standard Operating Procedures (SOPs) Qualification • A degree in Medicine (MBBS) or a post-graduation qualification (MD), preferably in a clinical branch • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) • Strong ability to evaluate and interpret data, synthesize scientific information, and write concise and accurate medical text Experience • Experience in drug safety, pharmacovigilance, or regulatory reporting is preferred • Fluency in written and spoken English • Ability to work with web-based applications and proficiency in computer skills in Windows 10/Windows 7 Skills • Ability to make concise, accurate, and relevant synopses of medical text and data • Attention to detail and strong analytical skills • Typing and transcription accuracyAbout The Company • Continuum India – A leading contract research organization (CRO) trusted by global leaders in the pharmaceutical and healthcare industries. Continuum India specializes in providing comprehensive services in the domains of pharmacovigilance, regulatory affairs, evidence evaluation, and technology solutions.

Role & Responsibilities • Review and assess asynchronous health questionnaires and pre-screening information • Conduct patient consultations via telephone and secure video platforms • Prescribe medications in accordance with relevant regulations following real-time telehealth calls • Escalate or refer patients to other healthcare professionals or services when clinically indicated • Maintain comprehensive, accurate, and timely clinical documentation • Ensure compliance with clinical governance, privacy, and data security standards • Deliver care that is patient-centered, culturally safe, and evidence-based Qualification • Medical degree recognized in Australia • Current AHPRA registration with no restrictions • Appropriate medical indemnity insurance to cover telehealth consultations • Registration in New Zealand is advantageous Experience • Previous experience in telehealth settings and/or general practice settings • Confidence in conducting consultations via phone and video • Excellent communication and rapport-building skills Skills • Competence with digital health systems and electronic medical records • Ability to work independently in a remote setting • Strong attention to detail in clinical documentation • Familiarity with telehealth platforms and clinical systems Compensation • $175 per hour • Up to 20 hours per week (fully remote) Benefits • Flexible, part-time hours within standard business times (Preferred days: Monday to Wednesday, 8am-4pm) • Opportunity to cover after-hours and weekends • Work with an established digital healthcare service providing safe, convenient online consultations About The Company • Simple Online Healthcare – Founded in 2015, Simple Online Healthcare started as a small pharmacy and has grown into a trusted digital healthcare service.

Role & Responsibilities • Provide high-quality care to patients at the new trial Comprehensive Symptomatic and Diagnostic Breast Clinic at The Prince Charles Hospital (TPCH), Chermside • Treat and manage breast patients at both Herston and Chermside facilities • Actively participate in quality activities including patient safety, clinical audit, research, and service planning for the Breast Health Outpatient Department and Comprehensive Symptomatic and Diagnostic Breast Clinic • Collaborate with primary care organizations and practitioners (e.g., general practitioners) • Prepare appropriate correspondence to patients, primary care organizations, and primary care practitioners • Undertake training necessary to utilize IT systems required in the role • Support the health equity agenda, promoting culturally safe and responsive health services, and contributing to the elimination of racial discrimination Qualification • MBBS or equivalent medical degree • Postgraduate qualifications in Breast Surgery or relevant experience in the field of breast health Experience • Experience in general practice with a special interest in breast surgery • Ability to work collaboratively with multidisciplinary teams • Strong interest and experience in quality improvement and patient safety initiatives Skills • Strong communication and interpersonal skills • Excellent clinical decision-making and diagnostic skills • Ability to work independently and manage a busy caseload • Proficiency in using IT systems for patient management and documentation Compensation • $94.59 - $101.12 per hour Benefits • Career and development opportunities across various clinical and non-clinical areas • Flexible working arrangements and competitive salary rates with annual incremental increases • Higher employer contribution to superannuation (up to 12.75%) and access to salary packaging • Work-life balance in a safe, satisfying, and flexible work environment • Opportunities for professional development in a dynamic health service • Access to a diverse and inclusive workplaceAbout The Company • Metro North Hospital & Health Service (HHS) – As one of the largest and most comprehensive health services in Queensland, Metro North HHS is committed to providing exceptional healthcare, research, and education.

Role & Responsibilities • Provide high-quality primary care services at the Hughenden Doctors Surgery as a salaried medical officer • Deliver general practice services as an integral part of the healthcare team • Manage and treat a wide range of medical conditions and provide patient care • Collaborate with multidisciplinary teams for patient management and complex cases • Participate in clinical research and contribute to innovative healthcare solutions • Provide health education and preventive care to patients • Document and manage patient records and treatment plans accurately Qualification • Medical qualification with registration or membership with the appropriate registration authority or association • Mandatory qualification as per the role requirements Experience • Experience in general practice or primary care settings • Experience working with multidisciplinary teams • Familiarity with rural healthcare practices and patient management Skills • Excellent clinical judgment and decision-making skills • Strong communication and interpersonal skills • Ability to work independently and collaboratively with a team • Ability to manage a wide variety of medical cases and conditions • Proficiency in using healthcare management systems Compensation • Salary range: $187,569 to $274,678 p.a. (L13 - L27) • 4 to 6 weeks annual leave with 14%-17.5% loading • 12.75% employer contribution to superannuation • Additional benefits: Motor Vehicle Allowance, Professional Development Allowance, Inaccessibility Incentive Allowance (category 2) • Salary Sacrificing options may be available About The Company • Townsville Hospital and Health Service (HHS) – A leading tertiary and referral service, offering cutting-edge medical practices, advanced research, and specialized clinical expertise.

Role & Responsibilities • Provide medical care and treatment for patients in a family medical practice setting • Conduct patient assessments, take medical histories, and perform physical examinations • Diagnose medical conditions and provide treatment or referrals as necessary • Prescribe medications and offer lifestyle advice to patients • Maintain accurate medical records and treatment plans • Participate in telehealth consultations (work from home one day a week) • Collaborate with on-site pathology, reception staff, and allied health workers (speech pathology) • Be available for patient care with no weekend work required Qualification • Vocationally Registered General Practitioner (VR GP) • Registered with the Australian Health Practitioner Regulation Agency (AHPRA) Experience • Experience as a GP, with a preference for candidates who have worked in a similar practice setting • Experience with telehealth services is a plus Skills • Excellent diagnostic, decision-making, and clinical skills • Strong communication and interpersonal skills • Ability to work independently and as part of a collaborative healthcare team Compensation • $180 – $250 per hour, with 80% of billings • Guaranteed $250 per hour (negotiable) plus superannuation • Generous sign-on bonus Benefits • Employee discount • Profit sharing • Salary packagingAbout The Company • Minchinbury Health Services – An established family medical practice located in the close-knit, caring community suburb of Minchinbury, Western Sydney.

Roles & Responsibilities • Support clinical research activities as per assigned role • Assist in data collection, documentation, and compliance activities • Follow SOPs, GCP guidelines, and regulatory requirements • Coordinate with internal teams for smooth study execution • Ensure accurate reporting and timely completion of assigned tasks Qualifications • Relevant degree in Pharmacy / Life Sciences / Clinical Research or related field Experience • 0 to 5 years of relevant experience • Freshers with strong interest in clinical research can apply Skills • Good communication and documentation skills • Basic knowledge of clinical research processes and guidelines • Attention to detail and ability to work in a team • Willingness to work full-time in an on-premise setup About the Organisation ADVITY Research is a clinical research organization focused on delivering high-quality research services, fostering talent, and building careers in the clinical research domain.

Roles & Responsibilities • Assist in regulatory documentation and compliance-related activities • Support preparation, review, and maintenance of regulatory submissions • Gain hands-on exposure to regulatory processes under expert guidance • Coordinate with internal teams for data collection and documentation • Support ongoing regulatory projects and new initiatives • Follow company SOPs and regulatory guidelines Qualifications • B.Pharm / M.Pharm / MD / BDS / BAMS / BHMS Skills • Strong interest in Regulatory Affairs • Good communication and documentation skills • Fluency in English, Hindi, and Marathi • Willingness to learn and adapt in a professional environment Additional Details • Working Days: Monday to Friday • Travel Allowance provided • Opportunity for payroll absorption for high-performing interns About the Organisation Agenome Research is a research-driven organization offering practical, real-world exposure in regulatory affairs, focused on developing skilled professionals through hands-on training and expert mentorship.

Roles & Responsibilities• Perform general dental procedures and provide comprehensive oral care to patients• Assess patients’ dental conditions and diagnose oral health issues• Develop and execute appropriate treatment plans• Manage day-to-day clinic operations and support smooth functioning of the clinic• Maintain accurate medical records and dental documentation• Educate patients on oral hygiene, preventive care, and post-treatment instructions• Ensure adherence to clinical protocols, hygiene, and safety standards• Coordinate with clinic staff to deliver efficient and patient-focused careQualifications• Bachelor’s degree in Dental Surgery (BDS)• Valid dental registration/license to practiceExperience• Freshers or candidates with relevant clinical experience may apply• Experience in general dentistry and clinic management is an advantageSkills• Patient assessment and clinical evaluation• Knowledge of medical terminology and dental procedures• Medical documentation and record management• Good communication and interpersonal skills• Ability to manage clinic responsibilities independentlyAbout the CompanyThe Mosaic Dental is a patient-centric dental clinic in Bengaluru, committed to delivering quality dental care in a professional and comfortable environment. The clinic focuses on ethical practice, accurate diagnosis, and personalized treatment, ensuring high standards of oral healthcare for every patient.

Role & Responsibilities • Lead the development and delivery of clinical education programs for patients, clinicians, and diabetes societies, promoting CGM technology • Serve as a subject matter expert at local, regional, and international congresses, providing technical and clinical insights on CGM • Collaborate with Medical/Clinical Affairs, Marketing, R&D, Regulatory, Quality, Customer Support, and Field Sales teams to meet customer needs • Drive KOL (Key Opinion Leader) development, identify CGM advocates, and facilitate partnerships to establish CGM as the standard of care • Support distributors with clinical education and sales training, delivering tailored programs to accelerate product adoption • Work closely with regional stakeholders to assess training needs, update curriculum, and implement best practices across markets • Develop and maintain training resources, including leveraging Learning Management Systems (LMS) for ongoing learning initiatives • Provide coaching and feedback to distributor partners to enhance sales effectiveness and market penetration • Travel up to 50% for high-volume cycles and adapt to diverse environments and stakeholder needs Qualification • Licensed Medical Doctor (MD), Dietitian (RD/LD), Registered Nurse (RN), or relevant clinical degree required • MD with specialist diabetes experience or Certified Diabetes Educator preferred Experience • Minimum 4 years of experience in diabetes education and treatment, with at least 2 years focused on CGM • Typically requires a bachelor’s degree and 10+ years of related experience, or a graduate degree with 6+ years • Proven experience in sales training, program design, and diabetes-related medical device sales • Experience working on regional strategy or partnership initiatives preferred • Previous management or lead experience with global brand and distributor frameworks is a plus Skills • Familiarity with advanced diabetes technologies, including CGM, and emerging diabetes therapeutics • Excellent verbal and written communication skills in English; proficiency in Southeast Asian languages is a plus • Expertise in designing and delivering training programs for diverse audiences, both virtually and in-person • Highly organized, adaptable, and able to manage multiple priorities in a remote, fast-paced environment • Strong project management, problem-solving, and interpersonal skills • Ability to work independently and develop innovative approaches to unique challenges About The Company • Dexcom – A global leader in continuous glucose monitoring (CGM) technology, dedicated to helping people with diabetes manage their condition and live healthier lives. Dexcom is committed to innovation and is driven by a mission to improve health outcomes across the world.

Role & Responsibilities • Manage antenatal, intrapartum, and postnatal care, including high-risk pregnancies • Conduct normal vaginal deliveries, assisted deliveries, and emergency & elective LSCS (Lower Segment Cesarean Section) • Independently handle obstetric emergencies • Provide gynecological consultations and perform necessary gynecological procedures • Coordinate with pediatricians for neonatal care and ensure smooth handover • Timely escalate to senior consultants when clinically indicated • Work collaboratively with nursing, anesthesia, pediatrics, and OT teams Qualification • Minimum 2-4 years of post-qualification clinical experience (flexible based on competency) • Proven experience in independently handling obstetric emergencies Experience • Strong clinical judgment and prompt decision-making skills • Experience in both routine and high-risk obstetrics and gynecology • Ability to work in a collaborative environment with other healthcare teams Skills • Excellent clinical and decision-making skills in obstetrics and gynecology • Ability to handle obstetric emergencies independently • Strong communication skills with patients and medical teamsKey Benefits • Exposure to IVF and high-risk pregnancy cases, with the opportunity to work closely with the IVF and fertility team • Additional compensation for emergency calls, night emergencies, and unscheduled procedures • Separate per-delivery / per-LSCS remuneration, over and above fixed or OPD compensation • Good delivery volume, ensuring consistent clinical exposure and procedural experience • Well-supported emergency setup, including in-house OT, anesthesia, pediatrics, blood bank tie-ups, and trained nursing staff About The Company • Thakral Hospital and Fertility Centre – A renowned hospital in Gurugram offering high-quality IVF, maternity, and surgical services. With over 21 years of experience, the hospital is known for its expert doctors, advanced facilities, and affordable care. The facility provides personalized and compassionate care, ensuring trust and well-being for individuals and families.

Roles & Responsibilities• Visit patients at their location and conduct dental consultations along with the assigned team• Perform consultations using advanced digital and diagnostic technologies• Manage patient records, case details, and appointment schedules• Ensure accurate documentation and follow-up coordination• Participate in training programs provided by the organization• Maintain high standards of clinical quality and patient experience• Commit to continuous learning and clinical excellence• Work within a 5–10 km radius of the assigned home zoneQualifications• Bachelor of Dental Surgery (BDS) from a recognized institutionExperience• 0–2 years of experience• Freshers are eligible to applySkills Required• Basic clinical knowledge and willingness to learn digital dentistry workflows• Good communication and patient-handling skills• Ability to manage records and appointments efficiently• Comfort with technology-enabled consultations• Professional attitude and adaptability to field-based workPerks & Benefits• Travel allowance (additional)• Health insurance• Provident Fund (PF)• Leave encashment• Other leave benefits as per company policyAbout the CompanyClove Dental is India’s largest network of dental clinics, known for delivering standardized, ethical, and technology-driven dental care across the country. With a strong focus on clinical excellence, patient safety, and innovation, Clove Dental provides dentists with structured training, advanced tools, and growth-oriented career opportunities while serving millions of patients every month through its extensive clinic network.

Role & Responsibilities • Lead and manage pharmacovigilance activities for drug safety • Evaluate and process adverse event reports to ensure regulatory compliance • Review and analyze safety data from clinical trials and post-marketing surveillance • Prepare and submit pharmacovigilance reports, including PSURs and DSURs • Provide safety expertise in interactions with regulatory authorities and health professionals • Collaborate with cross-functional teams to ensure compliance with global safety regulations • Mentor junior team members and contribute to continuous process improvements Qualification • MBBS/MD or equivalent medical degree Experience • 2-4 years of experience in Pharmacovigilance or Drug Safety • Hands-on experience with safety databases and ICSR processing Skills • Strong understanding of global pharmacovigilance regulations • Excellent communication and interpersonal skills • Ability to analyze and interpret clinical data • Detail-oriented with strong problem-solving skills • Ability to work collaboratively in a team-oriented environment About The Company • APCERLS – A global provider of pharmacovigilance and regulatory affairs services, dedicated to supporting the healthcare industry with innovative safety solutions and regulatory compliance across various therapeutic areas.

Role & Responsibilities • Conduct initial assessments of patients, take medical histories, and perform physical examinations • Diagnose medical conditions based on patient information and clinical findings • Provide immediate treatment for acute and emergency medical conditions • Prescribe medication and treatment plans in accordance with best practices and patient needs • Monitor patient progress and adjust treatment plans as necessary • Provide counseling and health advice to patients and their families on diagnosis, treatment options, and preventative care • Respond promptly to emergency medical situations (trauma, cardiac arrest, respiratory distress, etc.) • Perform emergency procedures such as resuscitation and stabilization when required • Collaborate with nurses, specialists, and other healthcare professionals to ensure coordinated patient care • Maintain clear, accurate, and up-to-date patient records in the hospital’s electronic health system • Communicate diagnoses, treatments, and procedures effectively to patients and their families • Supervise and guide junior doctors and medical students during their shifts • Ensure compliance with hospital policies, ethical standards, and legal requirements Qualification • Medical Degree (MBBS or equivalent) • Registered with the Medical Council or relevant professional board Experience • 1 year of clinical experience in general medicine, emergency care, or a relevant specialty (preferred) • Experience in a hospital or clinical setting is advantageous Skills • Excellent diagnostic, decision-making, and clinical skills • Strong communication and interpersonal skills • Ability to remain calm under pressure and make quick decisions in emergency situations • Proficiency in using hospital management systems and medical equipment About The Company • Harsha Institutions – A healthcare provider dedicated to delivering quality medical services to the community. The institution offers a range of services and is committed to providing high-quality patient care across multiple departments.

Role & Responsibilities • Engage with patients and explain HexaHealth’s specialized services, ensuring they understand the benefits and support available for high-acuity care • Assess patient health profiles and recommend suitable specialists and hospitals, coordinating consultations and ongoing treatment • Review and explain patient medical reports, offering guidance on treatment options and addressing patient concerns • Provide continuous patient support throughout their healthcare journey, offering empathetic assistance and resolving queries • Build strong relationships with hospitals and doctors, enhancing your expertise and offering informed patient support • Drive patient engagement, contributing to conversion rates and revenue growth by supporting well-informed healthcare decisions Qualification • MBBS, BDS, BAMS, BHMS, BUMS, or any medical-related qualification Experience • Freshers or candidates with experience in a business development role in healthcare or related sectors Skills • Patient-centric attitude with the ability to effectively handle multiple tasks • Proactive mindset with excellent problem-solving skills • Strong communication skills with the ability to engage and educate patients • Flexibility and adaptability in a dynamic healthcare environment About The Company • HexaHealth – A leading healthtech platform dedicated to helping patients select the right hospital or surgeon for their surgical procedures. HexaHealth is committed to creating India’s largest hospital network, ensuring a seamless and stress-free experience for patients throughout their healthcare journey.

Role & Responsibilities • Examine patients, take medical histories, address concerns, and answer questions • Diagnose and treat injuries, illnesses, and disorders • Order, perform, and interpret diagnostic tests, explaining results to patients • Counsel patients on diet, hygiene, preventive healthcare, and lifestyle changes • Update patient charts and information to reflect current findings and treatments • Recommend and design personalized treatment plans • Prescribe medications or therapies based on diagnoses • Explain medical procedures to patients clearly and effectively • Consult with other physicians and specialists when necessary, and work collaboratively with healthcare staff (nurses, assistants, etc.) • Comply with medical laws and regulations (e.g., HIPAA) Qualification • Medical degree with successful completion of a residency and internship • State license and certification to practice medicine Experience • 1-5 years of experience in general medicine • Knowledge and experience in diagnosing and treating a wide variety of illnesses Skills • Strong communication and interpersonal skills • Excellent leadership, organizational, and problem-solving abilities • High attention to detail and dexterity • Patience and compassion for patients • Willingness to stay updated on advancements in the medical field About The Company • Healthcare Consultant Private Limited – A healthcare consultancy focused on providing high-quality medical services across various specialties. The company emphasizes patient care, professionalism, and continuous development in healthcare solutions.