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Role & Responsibilities • Provide medical assessment and clinical care to admitted patients across medical, surgical, and rehabilitation wards • Conduct admission evaluations and order appropriate diagnostic investigations • Collaborate with Visiting Medical Officers (VMOs), nurses, and allied health professionals • Respond to clinical emergencies and initiate first-line management • Maintain accurate, timely, and comprehensive patient documentation • Participate in clinical handovers and multidisciplinary team meetings • Ensure adherence to hospital policies, patient safety standards, and clinical governance protocolsQualification • MBBS or equivalent medical degree • General Registration with AHPRA Experience • Minimum 3 years of postgraduate clinical experience • Experience in acute hospital care preferred • Advanced Life Support (ALS) certification desirableSkills • Strong clinical reasoning and patient management skills • Ability to handle emergency situations effectively • Excellent communication and teamwork abilities • Good documentation and clinical record-keeping skills • Commitment to patient safety and quality improvement • Ability to work in a multidisciplinary hospital environmentBenefits • Flexible casual shifts • Career growth within Ramsay Health Care national network • Access to LinkedIn Learning & professional development programs • Education scholarships & leadership development pathways • Employee discounts through Ramsay Rewards • Hospital, allied health & pharmacy cover discountsRequirements • National Police Check (within last 12 months) • Proof of immunisation as per hospital policyAbout the Company Cairns Private Hospital is a modern, well-equipped private healthcare facility delivering comprehensive medical and allied health services. It is part of Ramsay Health Care, one of Australia’s leading private hospital groups, known for innovation in patient care, robotic-assisted surgery, and strong clinical safety programs like the Ramsay Rule and Speak Up for Patient Safety initiative.

Role & Responsibilities • Provide comprehensive primary healthcare services to patients • Conduct consultations, diagnosis, treatment, and follow-up care • Manage chronic disease, preventive care, and general medical cases • Deliver women’s health, skin health, and procedural services (if interested) • Maintain accurate patient records and clinical documentation • Use digital tools such as AI medicale Lyrebird AI Scribe for efficient documentation • Work collaboratively with nursing and support staff • Ensure compliance with AHPRA, RACGP standards, and clinical guidelines • Participate in bulk billing and private billing servicesQualification • MBBS or equivalent medical degree • Vocationally Registered (VR) General Practitioner • FRACGP / FACRRM or equivalent fellowship • Current AHPRA Registration Experience • Experience in general practice preferred • Newly qualified VR GPs welcome • Experience in women’s health, skin procedures, or minor procedures is an advantageSkills • Strong clinical and diagnostic skills • Excellent communication and patient care approach • Ability to work in a fast-paced clinic environment • Comfortable using digital healthcare tools • Team-oriented with a collaborative mindset • Interest in procedural and preventive medicineBenefits & Earnings • $10,000 joining bonus • $250 per hour OR 70% of billing (first 6 months – whichever higher) • Average GP billing: $3,000–$3,500 per day • Potential additional $120,000 annual incentive (bulk billing incentive) • Full patient books from Day 1 • Flexible working hours • DPA locum opportunities available • Modern, fully equipped treatment roomsAbout the Company Toowong GP Superclinic and Montague Road 7 Day Medical Centre are well-established, high-volume medical centres located close to Brisbane CBD. The clinics provide modern facilities, strong patient demand, advanced digital systems, and a supportive clinical environment focused on quality patient care and work-life balance

Role & Responsibilities • Conduct telehealth consultations for patients across Australia • Perform clinical evaluations and follow-up consultations • Prescribe medications including S4 & S8 drugs in compliance with regulations • Maintain accurate clinical documentation and patient records • Use digital healthcare tools and telemedicine platforms efficiently • Collaborate with clinical support teams (nurses & doctors) • Ensure high standards of professional, ethical, and legal compliance • Participate in case discussions, clinical updates, and reporting • Support integrative care using lifestyle, conventional, and alternative approachesQualification • Medical Degree (MBBS/MD equivalent) OR • Nurse Practitioner qualification • Current AHPRA Registration (mandatory) Experience • Experience in telehealth or digital healthcare preferred • Clinical experience in general practice or primary care • Experience with medical cannabis (advantage, not mandatory — training provided)Skills • Strong clinical judgment • Excellent communication and patient engagement skills • Comfortable working independently in remote settings • Tech-savvy and confident with digital platforms • Organized with strong documentation skills • Team-oriented and collaborative mindsetAbout the Company Peace & Quiet Pty Ltd is an Australian telehealth clinic offering integrative healthcare that combines conventional medicine with natural, alternative, and lifestyle-based treatments. The organization focuses on sustainable, patient-centered care delivered through

Key Responsibilities Conduct detailed patient consultations and clinical evaluations. Review patient history, pre-consultation notes, and diagnostic inputs. Diagnose conditions and prescribe appropriate Ayurvedic medicines and therapies. Explain treatment plans, expected outcomes, and timelines clearly to patients. Address patient doubts and concerns in a calm, reassuring manner. Maintain accurate clinical documentation and prescriptions using standard formats. Guide and collaborate with junior doctors, nutritionists, and therapists on patient care. Monitor follow-ups and modify treatment plans as needed.Qualification BAMS (Bachelor of Ayurvedic Medicine & Surgery) – Mandatory MD (Ayurveda) – Preferred Valid registration with the State Ayurvedic Medical Council Experience 3–8 years of clinical experience in Ayurvedic practice Experience in managing chronic and lifestyle disorders is highly desirable Prior experience in a clinic/hospital/wellness center setup preferred Skills Strong Ayurvedic diagnostic and treatment planning expertise Proficiency in managing long-term and chronic conditions Excellent patient counselling and communication skills Ability to build trust and maintain strong patient relationships Good clinical documentation and prescription writing skills Team collaboration with therapists, nutritionists, and junior doctorsAbout the Company We are a progressive Ayurvedic healthcare organization focused on delivering authentic, evidence-based Ayurvedic treatments for chronic and lifestyle-related conditions. Our approach blends classical Ayurvedic wisdom with modern clinical practices, ensuring holistic and personalized patient care.

Key Responsibilities Provide clinical care to patients as per standard medical protocols. Conduct patient examinations, diagnose conditions, and recommend appropriate treatment plans. Monitor patient progress and maintain accurate medical records. Manage emergency cases and provide first-line treatment when required. Coordinate with consultants, nursing staff, and other healthcare professionals. Ensure compliance with hospital policies, safety standards, and medical ethics. Participate in ward rounds and follow-up patient careRequirements MBBS degree from a recognized medical college. Valid TNMC registration (mandatory). Strong clinical knowledge and diagnostic ability. Good communication and interpersonal skills. Willingness to work in shifts (if applicable). Strong commitment to patient care and safety. Preferred Skills Ability to work independently and within a team. Basic emergency and critical care management skills. Familiarity with hospital documentation and EMR systems (preferred). Benefits Competitive salary based on experience. Excellent clinical exposure and learning opportunities. Supportive and professional working environment. About the Company We are a patient-focused multi-specialty healthcare facility committed to delivering high-quality, ethical, and evidence-based medical care. With a dedicated clinical team and modern infrastructure, we provide comprehensive healthcare services while fostering a supportive environment for medical professionals to learn, grow, and excel in patient care.

Role & Responsibilities • Participate actively in client admission process from a medical and holistic continuum care perspective • Review medical records and assess clinical condition prior to admission • Conduct pre-admission medical assessment • Liaise with referring/primary clinicians when additional information is required • Present cases for internal medical board review when needed • Determine eligibility for CCF admission and document decisions • Recommend care optimization when admission criteria are not metQualification • MBBS (mandatory) • Master’s degree preferredExperience • Experience in rehabilitation, long-term care, palliative care, or hospital medicine preferred • Experience in multidisciplinary clinical settings desirableSkills • Strong clinical assessment and care planning skills • Knowledge of palliative and rehabilitative care • Excellent documentation (SOAP format) • Ability to work in multidisciplinary teams • Strong communication and counselling skills • Understanding of NABH and patient safety standards • Compassionate and patient-centric approach About the Organization Sukino Continuum Care Facility (CCF) provides integrated rehabilitative, recuperative, and palliative healthcare services through a multidisciplinary model.

Role & Responsibilities • Conduct high-quality scientific interactions with Key Opinion Leaders (KOLs) on disease science, clinical data, and treatment guidelines • Build and maintain long-term scientific relationships with healthcare professionals • Respond to unsolicited medical queries in a timely and compliant manner • Capture and submit actionable medical insights including product feedback and clinical perceptions • Support scientific education initiatives such as CMEs, RTMs, advisory boards, and medical programs • Deliver scientific training sessions for internal sales teams • Support medical strategy development and product launch activities • Facilitate research and evidence-generation activities such as IIS, RWE, and observational studiesQualification • BAMS or MD Experience • Freshers with strong interest and aptitude for medical/marketing roles are welcome • Experience in scientific communication or healthcare engagement is an advantageKey Skills & Competencies • Strong scientific knowledge and ability to interpret medical literature • Excellent communication and presentation skills • Ability to confidently engage senior clinicians in scientific discussions • Ability to work independently in a field-based environment • High ethical standards and compliance awareness • Adaptability to travel and field workBenefits • Cell phone reimbursement • Health insurance • Provident Fund About the Company We are a fast-growing healthcare organization committed to advancing scientific engagement and evidence-based medical practices across priority therapeutic areas.

Role & Responsibilities • Diagnose and manage a wide range of kidney-related disorders • Supervise and manage dialysis and hemodialysis treatments • Provide care for patients requiring kidney transplant evaluation and post-transplant follow-up • Develop and monitor individualized patient treatment plans • Manage acute and chronic renal failure cases • Collaborate with multidisciplinary medical teams for comprehensive patient care • Educate patients and families on kidney health and treatment options • Maintain accurate medical records and treatment documentation • Stay updated with advancements in nephrology practices and technologies Qualification • MD / DNB in Nephrology or relevant super-specialty • Strong academic background in General MedicineExperience • Experience working in a nephrology department or hospital setting preferred • Hands-on experience in dialysis and hemodialysis management • Experience handling critical renal care cases is an advantageSkills • Strong expertise in nephrology and renal disease management • Proficiency in dialysis procedures and patient monitoring • Clinical decision-making and diagnostic skills • Teamwork and coordination with other specialties • Excellent patient communication and counseling ability • Commitment to continuous professional developmentAbout Company Mithra Medicare Hospitals is committed to delivering compassionate, high-quality healthcare to underserved communities in Tier-2 cities across India. With advanced medical facilities and a patient-centric approach, the hospital focuses on making modern healthcare accessible and affordable.

Role & Responsibilities • Deliver undergraduate and postgraduate medical teaching as per curriculum • Conduct clinical teaching, ward rounds, and academic sessions • Guide students in research activities and academic projects • Participate in departmental seminars, case discussions, and CME programs • Provide patient care in assigned clinical departments • Maintain academic records and institutional documentation • Assist in curriculum planning and departmental academic development • Follow NMC guidelines and institutional protocolsQualification • Post-graduation in relevant medical specialty • MD / MS / DNB (Recognized qualification) Experience • As per NMC norms for Assistant Professor post • Teaching or clinical experience preferredSkills • Strong subject knowledge in concerned specialty • Teaching and mentoring ability • Clinical and diagnostic skills • Research orientation • Communication and presentation skills • Ability to work in academic and hospital environment• Total Vacancies: 97 • Age Limit: 21 – 45 years (Age relaxation as per norms) • Selection Process: Interview • Application Fee: No feeAbout Company APMSRB (Andhra Pradesh Medical Services Recruitment Board) is a government recruitment body responsible for appointing qualified healthcare professionals and faculty in medical institutions across Andhra Pradesh. 📅 Last Date: 27-01-2026Official NotificationClick Here

Roles & Responsibilities:• Assess patients’ physical conditions and functional limitations• Plan and deliver individualized physiotherapy treatment programs• Provide pain management, mobility improvement, and rehabilitation therapies• Monitor patient progress and modify treatment plans as required• Maintain accurate patient records and treatment documentation• Educate patients on exercises, posture correction, and injury prevention• Ensure adherence to clinic hygiene, safety, and treatment protocols• Deliver patient-focused, evidence-based physiotherapy careQualifications:• Bachelor of Physiotherapy (BPT) or Master of Physiotherapy (MPT)• Female candidates preferred• Freshers are welcome to applyExperience:• Fresher to relevant clinical experienceSkills Required:• Strong communication and patient-handling skills• Basic knowledge of physiotherapy assessment and treatment techniques• Compassionate and patient-focused approach• Ability to work independently and as part of a clinical team• Willingness to learn and adapt to clinical practicesBenefits:• Flexible work schedule• Supportive and professional clinical environmentAbout the Company:Muskan Physiotherapy Clinic is a patient-focused physiotherapy center in Bengaluru, dedicated to improving mobility, recovery, and overall physical well-being through evidence-based physiotherapy care. The clinic emphasizes personalized treatment, compassionate care, and professional growth, providing an excellent learning and practice environment for both freshers and experienced physiotherapists.

Roles & Responsibilities:• Diagnose and treat general dental conditions independently• Handle day-to-day clinic operations and patient flow• Perform comprehensive treatment planning and execution• Provide high-quality dental care aligned with clinical protocols• Communicate treatment plans clearly to patients• Adapt to and work effectively within a corporate clinical environment• Maintain accurate patient records and documentation• Ensure adherence to hygiene, safety, and sterilization standardsQualifications:• BDS / MDS from a recognized dental institution• Valid Dental Council registrationExperience:• Minimum 2 years of relevant clinical experience• Experience handling clinics independently is preferredSkills Required:• Strong clinical and treatment planning skills• Excellent communication and interpersonal abilities• Ability to manage patients independently• Professional attitude with adaptability to corporate cultureBenefits:• Health insurance• Provident Fund• Leave encashmentAbout the Company:Clove Dental is one of India’s leading dental care networks, offering standardized, technology-driven dental services across multiple cities. With a strong focus on clinical excellence, patient safety, and ethical practice, Clove Dental provides dentists an opportunity to work in a structured corporate environment while delivering high-quality oral healthcare.

Role & Responsibilities • Provide high-quality primary healthcare services to patients • Diagnose, treat, and manage acute and chronic medical conditions • Conduct patient consultations, health assessments, and follow-ups • Develop and implement patient management and treatment plans • Maintain accurate clinical documentation and medical records • Collaborate with nursing staff and other healthcare professionals • Participate in preventive healthcare and health educationQualification • Vocationally Registered (VR) General Practitioner • FRACGP, FACRRM, or equivalent fellowship • Full AHPRA Registration Experience • No minimum years required after obtaining VR status • Newly qualified VR GPs are welcome • Experience in general practice or private billing setup preferredSkills • Strong clinical decision-making and diagnostic skills • Excellent patient care and communication • Ability to work in a collaborative healthcare environment • Interest in expanding into cosmetic and skin cancer procedures • Professional, ethical, and patient-focused approachAbout Company Capstone Medical Centre (Southbank Medical Centre) has been serving the Melbourne community for over 18 years. It is a RACGP-accredited private billing clinic known for delivering high-quality, patient-centered care.

Roles & Responsibilities • Perform medical and scientific data review for hematology clinical trials (e.g., myeloma, lymphoma) • Review standard data listings including adverse events, concomitant medications, efficacy and safety data • Conduct patient profile reviews, safety narratives, PD analysis, and scientific data evaluations • Support Lead Clinical Scientist and Medical Director in medical data review activities • Develop and contribute to Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans • Author medical data queries, review responses, and support query closure • Participate in medical and safety review meetings, including slide preparation • Collaborate with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams • Identify data trends, risks, and subject safety issues; escalate concerns appropriately • Ensure compliance with ICH-GCP, data privacy standards, SOPs, and regulatory requirements • Support audits and trusted process meetings as required Qualification • Degree in Life Sciences: MSc, PharmD, PhD, MD, DMD or equivalent Experience • Relevant scientific or clinical research experience in clinical development • Exposure to medical data review, clinical trials, or drug development preferred Skills • Strong understanding of clinical trial data, scientific principles, and ICH-GCP guidelines • Excellent analytical, documentation, and problem-solving skills • Strong written and verbal communication abilities • Proficiency in MS Office (Word, Excel, PowerPoint) • Ability to manage multiple tasks in a regulated, fast-paced environment • Strong collaboration and stakeholder management skills About the Organisation Syneos Health® is a leading global biopharmaceutical solutions organization, supporting clinical development, medical affairs, and commercialization. With operations across 110+ countries and involvement in the majority of novel FDA and EMA approvals, Syneos Health partners with customers to accelerate the delivery of therapies that improve and save lives worldwide.

Roles & Responsibilities • Monitor adherence to prescribed dose status across global clinical trial sites • Identify dose discrepancies and drive timely, traceable follow-ups with sites • Document dose-related risks and maintain inspection-ready records • Conduct routine and ad-hoc dose surveillance reviews as per protocol • Collaborate with Trial Managers, Clinical Medical Managers, and Medical Advisors • Support site engagement through clear communication and data insights • Coach site staff on dose compliance, documentation quality, and protocol adherence • Communicate findings to trial teams and contribute to continuous improvement initiatives Qualification • Graduate degree in Life Sciences: M.Pharm, PharmD, Pharmacy, BDS/MDS, or MSc Nursing Experience • Minimum 2 years’ experience in clinical trials (Pharma/Biotech/CRO/Hospital) • Exposure to global clinical operations and trial systems Skills • Strong understanding of ICH-GCP and clinical trial conduct • Analytical mindset with ability to interpret clinical data • Excellent communication and stakeholder management skills • Ability to work independently in dynamic environments • Coaching and influencing skills with strong attention to detail About the Organisation Novo Nordisk is a global healthcare company with a strong legacy in clinical research and innovation. Through its Global Business Services in Bangalore, the company supports worldwide clinical development with advanced risk-based monitoring, data quality, and patient safety initiatives, contributing to high-quality and compliant clinical trials across the globe.

Roles & Responsibilities • Perform publishing and technical validation of regulatory submissions (eCTD/CTD/NEES/Paper) for the US market • Conduct final technical quality review of submission dossiers • Dispatch submissions to health authorities or affiliates as per regulatory timelines • Handle post-submission activities including acknowledgements, receipts, and metadata capture in RIM systems • Upload and manage health authority correspondence, commitments, and related documentation • Ensure compliance with ICH and FDA guidelines in a regulated, process-driven environment • Coordinate with internal stakeholders and ensure timely communication of submission status Qualification • Bachelor’s degree in Pharmacy, Medicine, Chemistry, or related Life Sciences discipline Experience • Relevant experience in Regulatory Affairs Operations / Regulatory Publishing within the pharmaceutical industry Skills • Strong knowledge of ICH and FDA guidelines (US market) • Hands-on experience with eCTD, CTD, NEES, and paper submissions • Expertise in publishing tools such as Liquent, DocuBridge, or similar systems • Advanced English communication skills • Good understanding of RIM systems and regulatory workflows • Time management, organizational, and multitasking skills • Attention to detail and quality-focused mindset • Flexibility to adapt in a fast-changing environment About the Organisation Genpact is a global advanced technology services and solutions company that helps leading enterprises drive digital transformation through data, technology, and AI. Known for its strong regulatory, life sciences, and operations expertise, Genpact supports global pharma companies with end-to-end regulatory and compliance solutions while fostering innovation and continuous growth.

Roles & Responsibilities • Secure regulatory approvals for new products (NDA, LCM) within defined timelines • Manage product lifecycle activities including submissions, variations, and renewals • Prepare and review regulatory submission dossiers and application forms as per country-specific Health Authority requirements • Coordinate with distributors, affiliates, and health authorities to ensure regulatory compliance • Handle regulatory documentation for tenders and special submissions • Update and maintain regulatory information in Veeva Vault within agreed timelines • Support labeling development, review promotional materials, and ensure compliance with local regulations • Monitor regulatory environment changes and support post-approval regulatory activities Qualification • Post-Graduation or equivalent degree in Science Experience • Minimum 5+ years of experience in Regulatory Affairs within the pharmaceutical industry • At least 3 years of experience working in cross-functional, international or affiliate environments • Experience handling interactions with Health Authorities preferred Skills • Regulatory submissions and lifecycle management • Health Authority interactions • Regulatory documentation and compliance • Veeva Vault (Regulatory systems) • Project management and prioritization • Cross-functional collaboration and stakeholder management About the Organisation Novo Nordisk is a global healthcare company with over a century of experience in developing innovative treatments for chronic diseases. Driven by a strong patient-centric mission, the organization focuses on delivering high-quality, compliant, and sustainable healthcare solutions across international markets.

Roles & Responsibilities:• Assist in the day-to-day functioning of the dental clinic• Conduct basic dental examinations and patient consultations• Support senior dentists during dental procedures• Provide preventive dental care and oral hygiene guidance to patients• Maintain accurate patient records and clinical documentation• Ensure clinic hygiene, sterilization, and patient safety protocols• Deliver patient-focused and professional dental careQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institution• Valid Dental Council registrationExperience:• Freshers are welcome to apply• 0–1 year of clinical experience preferredSkills Required:• Basic clinical and diagnostic dental skills• Good communication and patient-handling abilities• Willingness to learn and work in a clinical setup• Professional attitude and teamwork skillsBenefits:• Flexible work schedule• Paid sick leave• Leave encashmentAbout the Company:STAR Dental Clinic and Implant Center is a patient-focused dental care provider committed to delivering quality dental treatments in a safe and professional environment. The clinic offers comprehensive dental services with an emphasis on ethical practice, continuous learning, and patient satisfaction.

Roles & Responsibilities • Support project monitoring and coordination using project management tools • Prepare study safety documents including SAE reporting forms and guidelines • Develop training materials for investigator meetings and safety trainings • Generate progress reports, listings, and study-related outputs for PVSM and clients • Assist in SAE and ICSR processing as per protocols, SOPs, and regulatory guidelines • Maintain and update internal safety databases • Follow up with investigator sites for query resolution • Prepare high-quality case narratives for safety reporting • Distribute ICSRs to Ethics Committees, Investigators, and MAHs • Prepare and circulate 6-monthly SUSAR line listings • Support preparation and submission of DSURs to Competent Authorities and Ethics Committees • Assist with MedDRA coding in coordination with Data Management and Statistics teams • Support additional pharmacovigilance activities as per departmental requirements Qualification • Degree in Pharmacy, Life Sciences, or related discipline Experience • Relevant experience in Pharmacovigilance, Clinical Research, or Safety Operations Skills • Pharmacovigilance processes and SAE / ICSR reporting • Safety database handling and case processing • MedDRA coding knowledge • ICH, EMA, and FDA regulatory guidelines • Microsoft Office and database management tools • Strong documentation, coordination, and communication skills About the Organisation Veeda Clinical Research is a leading global CRO providing comprehensive clinical research, bioanalytical, and pharmacovigilance services. The organization is known for its regulatory expertise, quality-driven processes, and strong presence in domestic and international clinical research.

Roles & Responsibilities:• Examine, diagnose, and treat dental and oral health conditions• Perform dental procedures as per clinical requirements• Develop and explain treatment plans to patients• Educate patients on oral hygiene and preventive dental care• Maintain accurate patient records and treatment documentation• Follow standard clinical protocols and safety guidelines• Ensure high standards of patient care and professionalismQualifications:• Bachelor of Dental Surgery (BDS) or Master of Dental Surgery (MDS) from a recognized institution• Valid Dental Council registrationExperience:• 0–5 years of clinical experience• Freshers and experienced candidates are welcome to applySkills Required:• Strong clinical and diagnostic skills• Good communication and patient-handling abilities• Professional and patient-focused approach• Ability to work independently and as part of a clinical teamAbout the Company:Rightzone Resource Solutions Pvt. Ltd. is a professional staffing and healthcare recruitment organization that connects qualified medical and dental professionals with reputable healthcare facilities, ensuring quality patient care and career growth opportunities.