Doctor Jobs

Roles & Responsibilities:• Diagnose and treat oral and dental health conditions• Perform general dental procedures and treatments• Assess patient conditions and recommend appropriate treatment plans• Provide high-quality, patient-centered dental care• Maintain accurate patient records and documentation• Ensure a safe, clean, and hygienic clinical environment• Follow standard sterilization and infection control protocolsQualifications:• Bachelor’s degree in Dental Surgery (BDS)• Relevant certifications and valid registrationExperience:• Prior clinical experience preferred• Freshers may applySkills Required:• Strong diagnostic and treatment planning abilities• Good communication and interpersonal skills• Attention to detail and commitment to patient safety• Professional and ethical clinical approachAbout the Company:PERFECT SMILE DENTAL CLINIC is a patient-focused dental practice located near Krishnapuri Matwari, Hazaribag, Jharkhand, dedicated to delivering quality dental care in a safe, clean, and comfortable environment.

Role & Responsibilities • Provide clinical care and treatment to patients as per hospital protocols • Assist senior consultants in diagnosis, procedures, and patient management • Participate in ward rounds, OPD, emergency duties, and clinical documentation • Ensure compliance with hospital policies and ethical medical practices • Support academic, research, and teaching activities as assignedName of the PostsVacanciesEducationSenior Resident14MBBS, DNB, MD/MS, PGDM, Post-graduationExperience • Freshers and experienced candidates eligible as per RGSSH normsAge Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation applicable as per Government / Hospital rulesAbout Company • Rajiv Gandhi Super Specialty Hospital (RGSSH) is a government-run tertiary care hospital providing advanced medical services across multiple specialties.Starting date20-01-2026Closing date28-01-2026Official Notification and Application FormClick Here

Key Responsibilities • Process and triage Individual Case Safety Reports (ICSRs) as per SOPs and safety plans • Perform case data entry, MedDRA coding, and narrative writing • Conduct literature screening and safety reviews • Identify, manage, and reconcile duplicate ICSRs • Perform quality review of safety cases • Support xEVMPD submissions and SPOR/IDMP activities • Maintain safety trackers and ensure regulatory compliance (ICH GCP, GVP) • Submit documents to TMF and PSMF • Participate in audits and regulatory inspections • Collaborate with global cross-functional PV teams Education: • B.Pharm / M.Pharm / Pharm.D / BDSExperience: • Specialist I: 2+ years • Specialist II: 3.5+ yearsTechnical Skills: • Strong knowledge of ICH, GVP, and global PV regulations • Hands-on experience with safety databases • Understanding of Clinical Trial phases II–IV and post-marketing safety • Proficiency in MS Word, Excel, PowerPoint, OutlookSoft Skills: • Excellent communication and documentation skills • Strong attention to detail and organizational ability Why Join Syneos Health? • Work on global studies involving 675,000+ clinical trial patients • Exposure to global audits, inspections, and regulatory submissions • Strong internal mobility and career development programs • Inclusive Total Self culture promoting diversity and well-being • Competitive compensation and rewards

Key Responsibilities • Process and triage Individual Case Safety Reports (ICSRs) as per SOPs and safety plans • Perform case data entry, MedDRA coding, and narrative writing • Conduct literature screening and safety reviews • Identify, manage, and reconcile duplicate ICSRs • Perform quality review of safety cases • Support xEVMPD submissions and SPOR/IDMP activities • Maintain safety trackers and ensure regulatory compliance (ICH GCP, GVP) • Submit documents to TMF and PSMF • Participate in audits and regulatory inspections • Collaborate with global cross-functional PV teamsEducation: • B.Pharm / M.Pharm / Pharm.D / BDS Experience• Specialist I: 2+ yearsTechnical Skills: • Strong knowledge of ICH, GVP, and global PV regulations • Hands-on experience with safety databases • Understanding of Clinical Trial phases II–IV and post-marketing safety • Proficiency in MS Word, Excel, PowerPoint, Outlook Soft Skills: • Excellent communication and documentation skills• Strong attention to detail and organizational abilityWhy Join Syneos Health? • Work on global studies involving 675,000+ clinical trial patients • Exposure to global audits, inspections, and regulatory submissions • Strong internal mobility and career development programs • Inclusive Total Self culture promoting diversity and well-being • Competitive compensation and rewards

Role & Responsibilities • Provide video-based telehealth consultations to patients across Australia • Deliver safe, ethical, and patient-focused medical care via digital platforms • Maintain accurate clinical documentation in line with AHPRA standards • Utilize video conferencing tools confidently for remote consultations • Ensure high-quality care without physical OPD or hospital involvementQualification • MBBS or equivalent medical degree • FRACGP or FACRRM certification • Active General Registration with AHPRA (Medical Board of Australia)Experience • Registered and practicing General Practitioner • Telehealth experience preferred but not mandatory Skills • Strong clinical judgment and patient communication skills • Comfortable with video consultations and digital workflows • Professional, reliable, and patient-centric approach • Ability to work independently in a remote environmentEligibility Requirements • Australian-based practitioner • Valid medical indemnity insurance (or ability to obtain) • Legal right to work in AustraliaWhat We Offer • Set your own working hours – no minimum commitment • Work 4 to 20+ hours per week as per your preference • 100% remote – no clinic, no commute, no admin burden • Immediate patient demand • Clinical and administrative support • Supportive, clinician-friendly work cultureAbout Company • Online Doctor Consult is a fast-growing telehealth platform connecting patients with qualified doctors across Australia

Role & Responsibilities • Perform complex urological surgeries, including minimally invasive procedures (robotic-assisted prostatectomies, laparoscopic nephrectomies) • Ensure optimal patient outcomes and high-quality post-operative care • Diagnose and manage urological conditions in OPD and IPD settings • Collaborate with multidisciplinary teams for patient management • Maintain accurate clinical documentation and adhere to hospital protocolsQualification • MD / MS in Urology or Nephrology from a recognized institution • Cleared DHA exam (for applicants planning to work in Oman)Experience • Minimum 5 years post-PG clinical experience in Urology • Hands-on experience in advanced surgical proceduresSkills & Competencies • Expertise in surgical urology and minimally invasive techniques • Strong clinical judgment and patient care focus • Excellent communication and teamwork skills • Ability to work independently and manage surgical cases efficientlyAbout Company • Aster DM Healthcare is a leading healthcare provider across the GCC and India, Committed to delivering world-class patient care, advanced diagnostics, and innovative treatment solutions

Role & Responsibilities • Diagnose and manage medical, pediatric, and cosmetic dermatology cases • Perform dermatological procedures: biopsies, cryotherapy, laser treatments, minor surgeries • Provide aesthetic dermatology services (injectables, skin rejuvenation) if credentialed • Develop individualized treatment plans and educate patients on preventive skin care • Maintain accurate medical records and adhere to clinical governance standards • Ensure compliance with DHA/DOH/MOH regulations • Collaborate with multidisciplinary teams for optimal patient outcomesQualification • MD / MS Dermatology or MBBS with Dermatology specialization • Valid or eligible DHA/DOH/MOH Specialist Dermatology licenseExperience • Minimum 10 years post-specialization experience in dermatologySkills & Competencies • Strong clinical judgment and procedural skills • Patient-focused, ethical practice with high professionalism • Excellent communication skills; fluent in English and preferably Arabic • Ability to work independently and as part of a teamAbout Company • Zulekha Hospital LLC is a leading healthcare provider in UAE, delivering advanced patient-centered care, Committed to high-quality medical services, innovation, and clinical excellence

Role & Responsibilities • Review and interpret diagnostic imaging cases (CT, MRI, X-ray, Ultrasound) for AI training • Create and validate radiology-based diagnostic questions with structured clinical reasoning • Evaluate AI-generated radiology reports for diagnostic accuracy and clinical logic • Provide detailed, structured feedback to improve AI model reliability and performance • Assist in refining AI outputs to enhance medical imaging interpretation accuracy • Work independently using secure digital platforms for image review and annotation Essential Qualifications • Proven clinical experience in Radiology or Diagnostic Imaging • Currently practicing radiologists, fellows, or recent radiology residents are welcome • Strong clinical reasoning and attention to diagnostic detail • Excellent written English communication skills • Comfortable working with remote digital tools and imaging platformsProject Benefits • Fully remote role with flexible working hours (5–40 hours/week) • High hourly compensation with weekly international payments • Opportunity to work on cutting-edge AI healthcare technology • No emergency duties, patient care, or medico-legal liability • Ideal for professionals seeking flexible, high-impact AI collaborationEqual Opportunity Statement • Taskify AI is an equal opportunity employer • All qualified applicants are considered based solely on radiology expertise, clinical experience, and project requirements

Role & Responsibilities • Act as a scientific, non-promotional medical liaison between GSK and healthcare professionals • Engage HCPs (physicians, pharmacists, nurses, academic experts) for scientific exchange • Provide disease-state and product-related medical education aligned with medical strategy • Discuss emerging data, clinical trials, unmet medical needs, and patient access barriers • Collect, analyze, and communicate medical insights across the product lifecycle • Plan and manage territory scientifically, prioritizing key accounts and engagements • Support clinical research and investigator-initiated studies in collaboration with Medical Affairs • Work cross-functionally with Clinical, Commercial, and Market Access teams • Maintain up-to-date expertise in assigned therapeutic areas and GSK medicines • Ensure full compliance with GSK SOPs, Code of Conduct, and local regulations • Complete required training, documentation, and activity reporting on time • Participate in field medical initiatives and cross-functional medical projectsQualification • MD / PharmD / PhD or relevant Life Sciences degree • Equivalent scientific or clinical experience may be considered Experience • Preferred: 3+ years’ experience in pharmaceutical industry or similar environment • Prior experience in Medical Affairs, MSL, or Clinical Research is an advantage Skills • Strong scientific knowledge in clinical and pharmaceutical sciences • Ability to translate complex data into clear, concise medical communication • Excellent verbal and written communication skills (English mandatory) • Strong stakeholder engagement and networking abilities • Understanding of clinical development and basic biostatistics • Strategic territory planning and execution skills • High compliance, integrity, and patient-focused mindset • Willingness to travel as per role requirementsAbout Company • GSK is a global biopharma company focused on specialty medicines and vaccines , Core therapy areas: Respiratory, Immunology, Oncology, HIV, Infectious Diseases. Purpose-driven organization aiming to impact 2.5 billion lives by the end of the decade

Role & Responsibilities • Diagnose and manage cardiac conditions including CAD, arrhythmias, and heart failure • Perform and interpret cardiac investigations (ECG, Echocardiography, TMT, Holter monitoring, etc.) • Manage OPD and IPD cardiology patients • Provide timely care and support during cardiac emergencies • Collaborate with multi-specialty clinical teams for comprehensive patient care • Ensure accurate and NABH-compliant clinical documentation • Follow hospital protocols and quality standards Qualification • DM / DNB in Cardiology • Qualification must be recognized by NMCExperience • Freshers and experienced cardiologists are welcome to applySkills • Strong clinical expertise in cardiology • Proficiency in non-invasive cardiac diagnostics • Ability to handle emergency cardiac cases • Excellent communication and teamwork skills • Commitment to patient safety and quality careAbout Company • A reputed healthcare organization providing advanced cardiac care • Committed to clinical excellence and NABH standards • Offers a supportive environment for learning and professional growth

Role & Responsibilities • Lead clinical safety strategy across global drug development programs • Review and endorse Patient Risk Management Plans (PRMPs) • Drive proactive risk minimization strategies throughout product lifecycle • Represent Patient Safety on Clinical, Project, and Safety Management Teams • Lead safety surveillance, signal detection, evaluation, and labelling strategy • Provide strategic medical safety input into clinical development planning • Review and approve safety-related clinical documents (protocols, IBs, ICFs, study reports) • Provide medical input to periodic safety reports (PSURs, PBRERs, DSURs) • Contribute patient safety content to global regulatory submissions (NDA, BLA, MAA) • Respond to regulatory safety queries and label deviation requests • Collaborate with external partners, vendors, and licensing partners • Support safety agreements, licensing arrangements, and due diligence activities • Maintain inspection readiness and ensure compliance with global PV regulations • Mentor and guide junior safety physicians and team members • Escalate critical safety issues to senior leadership with integrity and clarityQualification • MD / MBBS with relevant specialty • Board-certified / residency-trained physician Experience • Extensive experience in Patient Safety / Pharmacovigilance • Strong background in clinical development and regulatory safety • Experience leading safety strategy for global development programsSkills • Deep expertise in global pharmacovigilance regulations and processes • Strong signal detection, risk management, and benefit–risk assessment skills • Excellent strategic thinking and clinical judgment • Proven cross-functional leadership and stakeholder management • Strong regulatory writing and safety documentation skills • Ability to influence senior stakeholders and external regulators • Excellent communication and decision-making skillsAbout Company • AstraZeneca is a global, science-led biopharmaceutical company , Focused on transforming patient outcomes through innovative medicinesClosing Date: 19 Feb 2026

Role & Responsibilities • Accurately interpret and report ECGs within defined turnaround time (TAT) • Review patient ECGs and deliver timely reports to hospitals, clinics, diagnostic centers, and nursing homes • Identify critical and emergency ECG findings and immediately escalate as required • Provide telephonic support and guidance to doctors and healthcare professionals • Ensure readiness and completeness of patient data before reporting • Maintain high standards of diagnostic accuracy and clinical quality • Support continuous ECG reporting services to aid critical patient care • Follow clinical protocols and ensure timely completion of reports Qualification • MBBS + MD (General Medicine / Internal Medicine) • MBBS + DNB (General Medicine / Internal Medicine) • MBBS + PGDCC / FNICExperience • Minimum 5+ years of post-MBBS clinical experienceSkills • Strong expertise in ECG interpretation and non-invasive cardiology • High attention to detail and diagnostic accuracy • Ability to handle critical and emergency cardiac cases • Excellent communication skills for doctor-to-doctor interaction • Ability to work independently in a remote setup • Time management and adherence to strict TATsOther Information • Shift Duration: 4-hour continuous fixed shift • Shift Options: • 9:00 AM – 1:00 PM • 10:00 AM – 2:00 PM • 11:00 AM – 3:00 PM • Weekly rotational day off • Open to Male & Female candidates • Compensation: Best in the market (based on experience)About Company • Tricog is a health-tech company focused on cardiovascular disease management • Combines hardware, algorithms, software, and medical expertise

Role & Responsibilities • Provide teleconsultations to patients via phone or video • Diagnose, treat, and manage general medical conditions • Issue digital prescriptions in compliance with telemedicine guidelines • Maintain accurate patient records, documentation, and follow-ups • Set and manage consultation fees, schedules, and availability • Conduct structured follow-ups as per clinical judgment • Communicate effectively with patients in an online consultation environment • Ensure ethical medical practice and patient confidentiality Qualification • MD / DM / DNB (General Medicine or relevant specialty) • Active medical registration in India (mandatory)Experience • Prior clinical practice experience preferred • Experience in OPD or telemedicine is an advantageSkills • Strong clinical decision-making and patient management skills • Comfortable with teleconsultation platforms and digital workflows • Ability to issue digital prescriptions and maintain electronic records • Good communication and interpersonal skills • Self-driven with interest in building an independent practice • Knowledge of Indian telemedicine guidelinesAbout Company • SwingBell Labs operates Prescrable.com, a doctor-friendly digital clinic platform,       Zero-commission model – doctors keep 100% of consultation fees

Role & Responsibilities • Perform medical review of adverse events for investigational and marketed products • Ensure accurate medical interpretation and assessment of safety cases • Work closely with Pharmacovigilance (PV/SPVG) teams for case consistency • Ensure compliance with global regulatory requirements and internal SOPs • Identify, assess, and manage potential safety signals and risks • Provide medical input for aggregate safety reports (PSURs, PADERs, Annual Safety Reports) • Interact with client safety and medical teams as required • Maintain up-to-date knowledge of drug development and safety information • Support mentoring and training of internal safety and case processing staff • Maintain compliance with corporate policies, SOPs, and project-specific guidelines Qualification • MD / MBBS / DO • Completion of an accredited residency Experience • 1–2 years of clinical practice experience (preferred) • Minimum 1 year experience in pharmacovigilance, epidemiology, or pharma/biotech industry preferredSkills • Strong knowledge of global pharmacovigilance regulations and processes • Hands-on experience with MedDRA, WHO-DRL, and safety databases (e.g., ARGUS) • Excellent medical review and safety assessment skills • Strong written and verbal communication skills (English proficiency required) • Proficiency in MS Office (Word, Excel, PowerPoint) and safety systems • Ability to work collaboratively and independently • Strong presentation, interpersonal, and influencing skills • Willingness to travel up to 10% if requiredAbout Company • Syneos Health® is a global biopharmaceutical solutions organization operating in 110+ countries , Partnered with 94% of FDA-approved and 95% of EMA-authorized products in recent years

Role & Responsibilities • Perform onsite monitoring visits in compliance with ICH-GCP and SOPs • Conduct interim monitoring visits as per study protocol and timelines • Ensure subject safety, data integrity, and protocol compliance • Review source documents, CRFs, and essential trial documents • Identify, document, and resolve site issues and deviations • Liaise with investigators, site staff, and study teams • Ensure timely follow-up and closure of monitoring findings • Maintain accurate monitoring reports and documentation Qualification • B.Pharm / M.Pharm / Pharm.D • BHMS / BAMS / BDSExperience • Minimum 2+ years of onsite clinical monitoring experience • Completion of at least 90+ onsite interim monitoring visits (mandatory)Skills • Strong knowledge of ICH-GCP and clinical trial regulations • Excellent documentation and report writing skills • Good communication and stakeholder management skills • Strong attention to detail and compliance mindset • Ability to work independently in a field-based roleAbout Company • IQVIA is a global leader in clinical research, healthcare intelligence, and data-driven innovation , Offers a diverse, inclusive, and growth-oriented work culture , Committed to improving patient outcomes through science and technology

Role & Responsibilities • Provide comprehensive medical review expertise to ensure high-quality clinical data • Review patient data to identify anomalies and ensure medical plausibility as per protocol • Perform structured medical data review from a clinician’s perspective • Support project management activities including issue escalation, workload planning, and process improvement • Track service performance and assist in root cause analysis and corrective actions • Ensure timely follow-up and resolution of compliance-related issues • Act as Subject Matter Expert (SME) for medical data review • Provide therapeutic area and indication training to clinical teams • Participate in project kick-off meetings, team meetings, and client interactions • Identify opportunities to improve efficiency and quality of deliverables • Maintain strong internal and client stakeholder relationshipsQualification • MBBS with 2+ years of experience • MD (any specialization) – Freshers or experienced Experience • Experience in clinical practice, medical data review, clinical research, or clinical trials • Prior experience in CRO, pharmaceutical, or medical data sciences environment preferredSkills • Strong understanding of clinical and medical data • Knowledge of medical terminology, pharmacology, anatomy, and physiology • Excellent communication, interpersonal, and customer-handling skills • Strong project management and organizational abilities • Ability to work independently with minimal supervision • Capability to manage multiple projects and competing priorities • Strong analytical, problem-solving, and decision-making skills • Customer-focused mindset with leadership and coaching abilitiesAbout Company • IQVIA is a global leader in clinical research services, healthcare     intelligence, and commercial insights , Supports development and commercialization of innovative medical treatments worldwide

Role & Responsibilities • Provide high-quality toxicological support for new and existing products • Perform literature and database searches to retrieve toxicological data • Review, analyze, and document safety data for ingredients, products, and technologies • Prepare ingredient monographs, toxicological assessments, safety statements, and product summaries • Summarize risk assessment data on various toxicological endpoints • Identify, analyze, and report project-relevant data from secondary sources and databases • Respond to consumer queries and regulatory agency questions with scientific accuracy • Ensure all reports contain latest, accurate, and relevant toxicological information • Work independently and collaboratively in project-specific teams • Actively participate in team discussions and knowledge-sharing activities Qualification • Master’s degree in Toxicology / Pharmacology / Life Sciences or related discipline Experience • 1–2 years of relevant experience in toxicology or safety assessment • Experience in on-demand research or regulatory support preferred Skills • Strong domain knowledge in Toxicology • Hands-on experience with toxicological and regulatory databases (ECHA, PCPC, EFSA, Toxplanet, Embase, PubMed, etc.) • Excellent scientific report writing and documentation skills • Strong written and verbal communication skills • Ability to work autonomously in a fast-paced environment • Proficiency in MS Office (PowerPoint, basic Excel) • Strong internet research and data screening skills About Company • A reputed, globally leading pharmaceutical organization • Focused on ensuring product safety through scientific excellence • Offers a performance-driven environment with strong learning and growth opportunities

Role & Responsibilities: • Provide Ayurvedic consultations to patients • Assess patient health conditions and medical history • Prescribe Ayurvedic treatment plans and medications • Guide patients on diet, lifestyle modifications, and preventive care • Monitor patient progress and modify treatment plans as required • Maintain accurate and updated patient records • Ensure ethical practice and patient confidentiality • Deliver compassionate, patient-centric careQualification: • BAMS (Bachelor of Ayurvedic Medicine and Surgery) – Mandatory • Valid registration with State Ayurvedic Medical CouncilExperience: • Prior experience in Ayurvedic consultation is required • Immediate joiners preferredSkills: • Strong consultation and diagnostic skills in Ayurveda • Fluency in Marathi (mandatory) • Good communication and patient counseling skills • Ability to build patient trust and rapport • Basic documentation and record-keeping skillsAbout Company: • Healthcare organization providing Ayurvedic consultation and treatment services

Role & Responsibilities: • Provide primary medical care to patients with injuries and common illnesses • Diagnose and treat acute and chronic medical conditions • Prescribe medications and ensure appropriate treatment plans • Advise patients on lifestyle changes, preventive care, and wellness • Answer patient queries and explain diagnoses and treatment options clearly • Maintain accurate and up-to-date patient medical records • Work across one or more specialties such as general medicine, family medicine, internal medicine, pediatrics, or anesthesiology • Ensure ethical practice, patient safety, and confidentiality Qualification: • MBBS degree from a recognized medical institution • Valid medical registration with State Medical Council / NMCExperience: • Freshers or experienced MBBS doctors can apply • Relevant clinical experience is an added advantageSkills: • Strong clinical and diagnostic skills • Excellent communication and interpersonal skills • Compassionate and patient-focused approach • Detail-oriented with good problem-solving abilities • Ability to work independently and as part of a healthcare teamAbout Company: • Healthcare organization committed to providing quality primary medical care