Doctor Jobs

Roles & Responsibilities: • Manage day-to-day medical coding operations. • Assign accurate diagnosis and procedure codes to patient charts. • Maintain minimum 95% quality and productivity standards. • Ensure adherence to internal and client-specific coding compliance policies. • Implement feedback provided by reporting managers to improve performance. • Follow organizational policies related to information security, HIPAA, and HR compliance. Qualification: • Life Science or Paramedical graduate. • No backlogs with complete semester mark sheets. Experience: • Freshers only. • Passed out between 2022 and 2024. • Immediate joiners preferred. Skills: • Strong analytical and logical thinking skills. • High attention to detail and accuracy. • Average written and spoken English communication skills. • Ability to learn medical coding standards and healthcare workflows. Assessment / Interview Process: • HR Interview. • Online Assessment – Anatomy & Physiology. • Medical Transcription (MT) Training. • MT-cleared candidates will be onboarded into Medical Coding training batch. Compensation & Benefits: • Competitive remuneration. • Annual performance-based bonus. • Standard industry benefits. • Relocation package as per company policy (for outstation candidates). About the Organisation: AGS Health is a global leader in healthcare revenue cycle management, combining AI-enabled technologies with expert services to support leading U.S. health systems, physician groups, and academic medical centers, with a global workforce of 12,000+ professionals serving over 100 clients across diverse care settings.

Role & Responsibilities • Build and maintain strong scientific relationships with Key Opinion Leaders (KOLs), HCPs, and medical associations • Conduct high-quality scientific engagement and medical discussions with healthcare professionals • Share accurate, up-to-date scientific and clinical information in a compliant manner • Act as a scientific bridge between the organisation and the medical community • Capture medical insights and field feedback to support medical strategy • Support medical education initiatives and scientific programs • Contribute to patient care improvement through evidence-based scientific exchange Qualification • Medical / Life Sciences qualification as per organisational requirement Experience • Prior experience in Medical Affairs or MSL role preferred • Field-based scientific engagement experience desirable Skills • Strong scientific understanding and ability to interpret medical literature • Excellent communication and relationship-building skills • Ability to engage healthcare professionals in meaningful scientific dialogue • Ethical mindset with strong compliance orientation • Ability to work independently in a field-based role About the Role • Opportunity to contribute to scientific advancement and patient care, Field-facing medical role focused on education, engagement, and insights

Role & Responsibilities • Serve as a trusted scientific expert for oncology therapy areas • Maintain deep, up-to-date scientific and clinical knowledge of disease areas, products, and competitors • Engage Scientific Experts and KOLs through high-quality scientific exchange • Respond to complex, unsolicited medical and scientific inquiries compliantly • Capture and communicate strategic medical insights to internal medical and cross-functional teams • Synthesize complex data into meaningful clinical insights and recommendations • Contribute actively to medical planning, strategy, and execution in Lilly India • Identify opportunities for collaborative research and external partnerships • Develop and execute strategic territory plans with clear prioritisation • Ensure all activities comply with internal policies, procedures, and regulatory requirements Qualification • Advanced degree in Health Sciences: PharmD, MD, or PhD (preferred) • Master’s or Bachelor’s degree in Health Sciences considered with ≥5 years relevant experience Experience • 2–3 years of relevant clinical or therapeutic experience with advanced degree • 5+ years of clinical, research, or industry medical/scientific experience for Master’s/Bachelor’s degree holders • Prior MSL or field-based experience in oncology highly preferred • Proven experience engaging Scientific Experts and KOLs Skills • Strong scientific acumen with excellent literature evaluation skills • Advanced communication and presentation abilities • Strategic thinking and data synthesis capability • High emotional intelligence and stakeholder engagement skills • Ability to work independently in the field and manage multiple priorities • Strong collaboration and cross-functional teamwork skills • Proficiency with field-based digital tools and scientific databases • High ethical standards and compliance orientation About the Company • Lilly is a global healthcare leader dedicated to discovery-driven innovation, Focused on improving patient outcomes across oncology and other critical diseases.

Role & Responsibilities • Act as the scientific bridge between the company and the medical community • Conduct high-quality scientific engagements with KOLs on disease science and clinical evidence • 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, and advisory programs • Deliver internal scientific training to sales and field teams • Support medical strategy development and promotional launch activities • Facilitate evidence-generation initiatives including IIS, RWE, and observational studies Qualification • BAMS or MD • Freshers with strong marketing attitude and scientific aptitude are welcome Experience • Prior MSL or field medical exposure preferred but not mandatory • Willingness to work in a 100% field-based role Skills • Strong scientific understanding and literature interpretation skills • Excellent communication and presentation abilities • Ability to engage senior clinicians in scientific dialogue • Independent working capability with high field adaptability • Strong ethical standards and compliance orientation Job Nature • 100% field-based role • Extensive travel within assigned territory • Occasional travel for CMEs, conferences, and internal meetings Benefits • Cell phone reimbursement • Health insurance • Provident Fund About the Company • Biotics Lab focuses on scientific engagement and medical education initiatives, Works closely with healthcare professionals across priority therapy areas

Role & Responsibilities:• Perform proper patient diagnosis and physical examinations• Assess and manage a wide range of physiotherapy cases• Deliver manual therapy and rehabilitation treatments• Provide home-visit physiotherapy services as required• Communicate treatment plans clearly to patients and caregivers• Monitor patient progress and modify treatment plans accordingly• Maintain basic patient records and treatment documentation• Ensure professional and ethical patient care at all timesQualifications:• Diploma in Physiotherapy (DPT) / Bachelor of Physiotherapy (BPT) / Master of Physiotherapy (MPT)Experience:• Freshers are welcome to apply• Prior experience in sports injury management or clinical physiotherapy is preferredSkills Required:• Strong knowledge of physiology and physical examination techniques• Hands-on skills in manual therapy• Good communication and patient-handling abilities• Ability to manage cases independently and work within a team• Willingness to travel for home visitsBenefits:• Flexible work scheduleAbout the Company:Sarwar Healthcare Pvt Ltd is a healthcare service provider offering physiotherapy and rehabilitation services with a focus on accurate diagnosis, effective treatment, and patient-centered care. The organization aims to deliver quality clinical and home-based physiotherapy services while supporting professional growth and learning.

Roles & Responsibilities: • Perform local safety case receipt, processing, data entry, QC tracking, and ICSR follow-up in line with agreed timelines. • Manage generic and client-specific safety email inboxes. • Register, triage, assign, and coordinate processing of vigilance cases. • Perform follow-up with local reporters for missing or additional information. • Respond to queries from clients and reporters. • Conduct periodic reconciliations to ensure complete and compliant handling of safety reports. • Support local pharmacovigilance activities as required. • Participate in audits, inspections, and implementation of corrective action plans. Qualification: • Bachelor’s or Master’s degree in Medicine, Pharmacy, Nursing, or a science-related field (or equivalent experience). Experience: • 2+ years of experience in Pharmacovigilance within a service provider environment. • Hands-on experience in safety case data entry and QC. • Experience working to strict timelines and managing client communications. • Knowledge of UK and EU PV regulations. • Strong pharmaceutical background with understanding of GVP, GCP, FDA, and drug safety regulations. • In-depth knowledge of PV principles, adverse event reporting, and causality assessment. Skills: • Excellent organizational and interpersonal skills. • Strong team-working capability. • Effective time management and prioritization skills. • High level of accountability and autonomy. • Process-oriented with strong attention to detail. • Clear written and verbal communication skills to explain complex concepts. • Flexible and adaptable in a dynamic work environment. • Ability to work under pressure and meet deadlines. • Safety database experience preferred. About the Organisation: ProductLife Group is a global life sciences consulting and services company delivering end-to-end solutions across pharmacovigilance, regulatory affairs, quality, and compliance, supporting pharmaceutical, biotechnology, and medical device companies worldwide throughout the full product lifecycle.

Roles & Responsibilities: • Perform quality control of vigilance cases. • Conduct medical evaluation of safety reports. • Data entry of vigilance cases into agreed databases/formats. • Follow-up of vigilance cases via phone and email. • Pre-analysis of complex cases prior to data entry. • Medical evaluation of files including coding, causality assessment, expectedness, and seriousness of events. • Identify submission requirements for each case. • Validate documents prepared by Data Managers/Vigilance Associates. • Close vigilance case files in compliance with regulations. • Define and implement ICSR/MLM filters and applicable changes. • Analyze inclusion/exclusion of EV/MHRA cases. • Provide medical information support and handle safety-related calls. • Review medical information queries and quality complaints to identify safety information. • Act as key contact for specific clients and prepare quality documents as required. Qualification: • Doctor of Pharmacy / Pharmacist Experience: • 1–3 years of experience in a similar Pharmacovigilance role • Knowledge of Pharmacovigilance is an advantage Skills: • Experience with safety databases preferred • Knowledge of current PV regulations • Process-oriented, detail-focused, and team player • Proficient in Microsoft Office tools • Strong multitasking and flexibility • Excellent communication skills in French and English About the Organisation: ProductLife Group is a global life sciences consulting and services company providing integrated solutions across pharmacovigilance, regulatory affairs, quality, and compliance, supporting pharmaceutical, biotechnology, and medical device companies worldwide throughout the entire product lifecycle.

Roles & Responsibilities:• Conduct detailed physical and functional assessments to identify musculoskeletal and movement-related issues• Develop and implement structured, personalized rehabilitation and treatment plans• Deliver evidence-based manual therapy and exercise prescription• Monitor patient progress and modify treatment plans as required• Maintain accurate clinical documentation and treatment records• Communicate effectively with referring physicians and internal teams• Educate patients on posture correction, injury prevention, and lifestyle modification• Collaborate with fitness advisors and multidisciplinary clinical teams• Participate in workshops, patient awareness programs, and community initiativesQualifications:• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT) from a recognized institution• Valid professional registration (preferred)Experience:• Experience preferred in musculoskeletal or sports injury rehabilitation• Freshers with strong clinical fundamentals are encouraged to applySkills Required:• Strong clinical reasoning and assessment skills• Sound knowledge of physiology and medical terminology• Excellent communication and patient interaction abilities• Ability to work efficiently in a high-volume clinical environment• Proactive, empathetic, and patient-focused approachAbout the Company:SPARRC is a leading rehabilitation and sports science organization dedicated to delivering evidence-based physiotherapy and movement therapy. Guided by scientific precision and a strong clinical philosophy, SPARRC focuses on holistic recovery, injury prevention, and long-term patient outcomes through multidisciplinary collaboration and community engagement.

Role & Responsibilities • Provide high-quality primary care services at Hughenden Doctors Surgery • Deliver comprehensive general practice services as a salaried medical officer • Manage acute and chronic medical conditions within a rural healthcare setting • Work collaboratively within a multidisciplinary healthcare team • Contribute to continuity of care and community-based health services • Support clinical governance, quality improvement, and patient safety initiatives • Participate in professional development, training, and service improvement activities Qualification • Mandatory qualification with appropriate medical registration authority • Awarded Scope of Clinical Practice (SoCP) • Current registration with relevant Australian medical board Experience • Experience in general practice or rural medicine preferred • Ability to manage diverse clinical presentations independently • Experience working in regional or remote healthcare settings desirable Skills • Strong clinical judgement and primary care expertise • Ability to work autonomously in rural environments • Effective communication and teamwork skills • Commitment to patient-centred, culturally safe care • Adaptability and resilience in regional healthcare delivery Additional Requirements • Possession of a Class C driver’s licence • Vaccine Preventable Disease (VPD) compliant • Ability to pass pre-employment checks including NDIS Screening • Probation period may apply Benefits & Lifestyle • 4–6 weeks annual leave with 14%–17.5% leave loading • Motor Vehicle Allowance and Professional Development Allowance • Inaccessibility Incentive Allowance (Category 2) • Salary sacrificing options available • Regional lifestyle with access to national parks and close-knit community About the Organisation • Townsville HHS is a leading tertiary and referral health service in Queensland,  Strong focus on clinical excellence, research, and professional development

Role & Responsibilities • Provide high-quality general practice care to a diverse patient population • Diagnose, treat, and manage acute and chronic medical conditions • Deliver preventive health care, health assessments, and patient education • Maintain accurate, compliant clinical documentation and records • Work collaboratively within a friendly, supportive clinic team • Uphold clinical governance, patient safety, and ethical standards Qualification • MBBS or equivalent medical degree • Fellowship with RACGP (all fellows accepted) • Current AHPRA registration Experience • Experience as a General Practitioner preferred • Ability to manage a broad range of primary care presentations Skills • Strong clinical judgement and diagnostic ability • Excellent patient communication and rapport-building skills • Commitment to high-quality, patient-centred care • Ability to work independently and within a team Additional Requirements • Right to work in Australia • Current Working With Children (WWC) Check • Current National Police Certificate • Valid Australian driver’s licence About the Company  • Busy, dynamic general practice located in Woori Yallock, Approximately 30–35 minutes from the Knox area

Role & Responsibilities • Provide high-quality general practice medical care to a diverse patient population • Diagnose, treat, and manage acute and chronic medical conditions • Deliver preventive healthcare, health assessments, and patient education • Maintain accurate and compliant medical records • Work collaboratively with nursing staff, pathology services, and support teams • Uphold clinical governance, ethical practice, and patient safety standards Qualification • MBBS or equivalent medical degree • General or Specialist registration with AHPRA • Eligibility to access Medicare Experience • Experience as a General Practitioner preferred • Ability to manage a broad range of primary care presentations Skills • Strong clinical judgement and diagnostic skills • Excellent patient communication and rapport-building ability • Commitment to high-quality, patient-centred care • Ability to work independently and as part of a multidisciplinary team About the Practice • Right Care Medical Centre was established in 2023 by experienced doctors, Provides      quality bulk-billing services in a busy Darwin suburban area

Role & Responsibilities • Provide continuous medical care to ICU patients including monitoring vitals and treatment response • Assist ICU consultants and specialists during patient management and emergency procedures • Perform regular clinical assessments and maintain accurate case sheets and documentation • Manage emergency situations including CPR, ventilator support, and stabilization of critical patients • Coordinate with nursing and paramedical staff for smooth ICU operations • Communicate patient condition updates to attendants as per hospital policy • Ensure adherence to hospital protocols, medical ethics, and patient safety standards • Participate in ICU ward rounds, audits, and quality improvement activities Qualification • BAMS (Bachelor of Ayurvedic Medicine and Surgery) – mandatory • Valid registration with respective State Medical Council Experience • Prior experience in ICU, Emergency, or Critical Care preferred • Exposure to hospital or acute care settings desirable Skills • Basic knowledge of ICU equipment and emergency protocols • Ability to handle high-pressure clinical situations • Sound clinical judgement and patient monitoring skills • Good communication and teamwork abilities • Commitment to patient safety and ethical medical practice About the Hospital • CritiCare Hospital is a multi-specialty healthcare facility in Lucknow, Focused on critical care, emergency services, and patient-centred treatment.

Role & Responsibilities • Diagnose and treat patients across common medical conditions • Prescribe medications and manage treatment plans as per clinical guidelines • Perform basic medical procedures with accuracy and care • Maintain complete and accurate medical records and documentation • Educate patients on disease management, medications, and preventive care • Collaborate with healthcare staff to ensure coordinated patient care • Ensure compliance with clinical standards, ethics, and patient safety protocols Qualification • MBBS degree from a recognised institution • Valid registration with Medical Council of India / State Medical Council Experience • Freshers and experienced MBBS doctors eligible • Clinical exposure in hospital or clinic settings preferred Skills • Strong diagnostic and clinical decision-making skills • Effective patient communication and counselling ability • Proficiency in medical documentation and electronic health records • Ability to perform basic clinical procedures confidently • Commitment to ethical medical practice and continuous learning About the Company • Medifit Solutions bridges the gap between doctors and healthcare institutions, Focused on placing skilled medical professionals in suitable healthcare roles. 

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) from spontaneous and organized data sources • Support review of trial-related adverse events and post-marketing adverse drug reactions • Ensure narrative consistency, seriousness, expectedness, and completeness of clinical information • Support MedDRA coding of adverse events under guidance • Assist with causality assessment and labeling evaluation • Collaborate with senior medical reviewers and team leads to ensure medical accuracy • Participate in quality checks and identify improvements in case documentation • Support audit and inspection readiness through compliant documentation • Contribute to internal trainings, workshops, and knowledge-sharing initiatives • Stay updated on evolving pharmacovigilance regulations and practices Qualification • Medical degree (MBBS or equivalent) • Valid medical license to practice Experience • 1–2 years of clinical experience • Prior exposure to pharmacovigilance or medical review required • Interest in drug safety, clinical data, and regulatory science Skills • Strong medical judgment and attention to clinical detail • Understanding of pharmacovigilance processes and ICSR workflows • Ability to apply MedDRA coding principles • Strong written and verbal communication skills in English • Collaborative mindset with ability to work in global teams • Process-oriented and quality-focused approach About the Company • Teva is a global biopharmaceutical company combining innovative medicines with a strong generics portfolio

Roles & Responsibilities • Support and independently execute research activities under ongoing projects at NABI. • Design, plan, and conduct experiments related to life sciences, biotechnology, or pharmaceutical research. • Analyze experimental data and prepare technical reports, presentations, and documentation. • Maintain laboratory records, project documentation, and ensure data integrity. • Assist in coordination of project activities, timelines, and deliverables. • Ensure compliance with laboratory safety guidelines, SOPs, and institutional policies. • Support procurement, inventory management, and maintenance of laboratory equipment. • Mentor junior research staff and provide technical guidance when required. • Participate in meetings, reviews, and scientific discussions related to project progress. Qualification • MD / MS, M.V.Sc, B.Pharm, MDS (from a recognized university / institution) Experience • Relevant research or project experience in life sciences, biotechnology, pharmaceutical sciences, or allied fields is preferred. • Experience in handling laboratory techniques, data analysis, and research documentation is desirable. Skills • Strong understanding of research methodologies and experimental design. • Good analytical, documentation, and reporting skills. • Ability to work independently and in a multidisciplinary team environment. • Proficiency in MS Office and basic research data tools. • Effective communication and coordination skills. Age Limit • Minimum Age: 21 Years • Maximum Age: 40 Years • Age relaxation as per NABI / Government of India norms. Walk-in Interview Details • Date: 03-02-2026 • Venue: National Agri-Food Biotechnology Institute (NABI), Knowledge City, Sector-81, Mohali, Punjab – 140306 About the Organisation National Agri-Food Biotechnology Institute (NABI) is an autonomous institute under the Department of Biotechnology, Government of India, dedicated to translational research in agri-food biotechnology to improve human nutrition, food security, and agricultural sustainability.Application formClick HereOfficial NotificationClick Here

Role & Responsibilities • Oversee adherence to prescribed dose status across assigned clinical trial sites • Identify prescribed vs expected dose discrepancies and drive traceable follow-ups • Collaborate with Clinical Medical Managers and Medical Advisors on dose-related issues • Document dose-related operational risks and maintain inspection-ready records • Execute routine and ad-hoc dose surveillance reviews as per protocol requirements • Support site engagement through clear communication and timely escalation • Partner with Trial Managers on dose and retention-related matters • Coach site staff on dose compliance, documentation quality, and protocol adherence • Communicate findings to trial squads and medical partners for informed decisions • Contribute to continuous improvement and development of surveillance processes Qualification • Graduate degree in Life Sciences (M.Pharm, PharmD, Pharmacy, BDS/MDS, MSc Nursing) • Strong understanding of clinical trial conduct and ICH-GCP Experience • Minimum 2 years’ experience in clinical trials (pharma/biotech/CRO/hospital) • Strong knowledge of clinical trial data, systems, and global operations • Experience working with cross-functional and global stakeholders Skills • Excellent communication and relationship-building skills • Strong analytical and problem-solving abilities • Familiarity with clinical IT systems and trial tools • Ability to work independently in dynamic environments • High ownership, motivation, and continuous improvement mindset • Ability to coach, influence, and manage stakeholders effectively About the Company • Novo Nordisk is a global healthcare company with over 100 years of innovation , Strong focus on patient safety, clinical quality, and data integrity

Role & Responsibilities • Create and answer complex radiology cases and diagnostic reasoning questions for AI model training • Review AI-generated radiology reports for accuracy, completeness, and clinical relevance • Analyse and rank AI model outputs to identify reasoning gaps, factual errors, or unsafe recommendations • Provide structured expert feedback to improve AI diagnostic logic and imaging interpretation • Contribute to enhancing AI performance in medical imaging and clinical decision support Qualification • Medical degree or currently pursuing (MD, DO, MBBS or equivalent) • Radiology training or experience from an accredited program Experience • Practicing or recently practicing radiologists, fellows, or radiology residents • Experience in clinical imaging interpretation preferred Skills • Strong clinical judgement and diagnostic reasoning skills • Ability to assess scientific rigor and clinical soundness • Excellent written English for technical review and feedback • Attention to detail and structured analytical thinking • Ability to work independently in a remote, project-based environment About the Company • Quik Hire Staffing provides remote and contract-based clinical and technical talent,   Supports advanced AI and healthcare research initiatives

Roles & Responsibilities:• Assess patients’ physical health, mobility, and functional limitations• Develop and implement personalized physiotherapy and rehabilitation programs• Provide evidence-based physiotherapy treatments to improve mobility, recovery, and overall physical well-being• Monitor patient progress and adjust treatment plans as required• Educate patients on exercises, posture correction, and injury prevention• Maintain accurate patient records and documentation• Ensure adherence to clinical protocols, safety, and hygiene standardsQualifications:• Bachelor’s (BPT) or Master’s (MPT) degree in PhysiotherapyExperience:• Freshers are welcome to apply• Relevant clinical experience is an advantageSkills Required:• Strong assessment and physiotherapy skills• Good communication and interpersonal abilities• Compassionate, patient-centered, and professional approach• Ability to work independently and as part of a clinical teamAbout the Company:Muskan Physiotherapy Clinic, Bengaluru, is a patient-focused clinic dedicated to improving mobility, recovery, and overall physical well-being. The clinic emphasizes evidence-based physiotherapy care, compassionate service, and flexible scheduling to meet patient needs.

Role & Responsibilities • Provide medical and scientific support across current and upcoming Medical Aesthetics portfolios • Own and drive Key Opinion Leader (KOL) identification, development, and engagement • Lead scientific exchange with HCPs and share insights with cross-functional teams • Advise on brand strategy and contribute to tactical planning with marketing teams • Execute Medical Affairs plans for Saudi Arabia and MEA region • Deliver scientific education and training initiatives across the aesthetics portfolio • Conduct field visits, advisory board meetings, and clinical trial facilitation • Serve as a medical resource for internal and external stakeholders • Support medical-marketing messaging and approval processes • Ensure pharmacovigilance, compliance, and ethical standards are maintained • Contribute to internal training, external education, and thought-leadership initiatives Qualification • Medical degree (MD) or advanced science degree (PhD) preferred • Master’s or Bachelor’s degree in a scientific discipline (including Pharmacy) considered with relevant experience Experience • Minimum 2–5 years’ experience in the pharmaceutical industry • Experience in dermatology, plastic surgery, or medical aesthetics preferred • Medical Affairs experience including advisory boards, publications, and scientific exchange • Proven experience developing and maintaining KOL relationships • Strong understanding of local Saudi market and multinational work culture • Based in Riyadh with willingness to travel as required Skills • Strong scientific communication and presentation skills • Strategic thinking and country-level planning capability • Ability to engage and influence HCPs, KOLs, and internal stakeholders • Leadership and persuasion skills across commercial and medical teams • In-depth understanding of medical aesthetics and clinical concepts • High ethical standards with strong compliance orientation • Fluent English (verbal and written) • Proficiency in MS Office and related tools About the Company • Allergan Aesthetics is part of AbbVie, a global biopharmaceutical leader , Focused on advancing innovation in medical aesthetics.