Bangalore Healthcare Jobs

Key ResponsibilitiesReview and evaluate AEs and SAEs; perform first-line clinical assessmentPrepare SAE narratives and collect follow-up safety informationMonitor and report safety data from trials, RWE, spontaneous reports, and literatureSupport DSMB / Safety Review Committee activitiesEnsure timely regulatory safety submissions (FDA, EMA, etc.)Maintain and reconcile safety databasesPerform MedDRA and WHO Drug codingContribute to SaMPs, protocols, SOPs, and CRFsEnsure compliance with GCP, GVP, and global regulationsParticipate in audits and quality improvement initiativesQualificationsBachelor’s degree in Pharmacology, Nursing, Life Sciences, or related field1–2 years experience in Pharmacovigilance / Clinical Safety preferredFreshers considered with relevant internships, projects, or PV certificationsRequired SkillsStrong knowledge of GCP, GVP, and GxP principlesGood clinical judgment and scientific writing skillsHigh attention to detail and strong organizational skillsEffective communication and teamwork in global settingsWhy Emmes GroupGlobal CRO with strong scientific reputationExposure to international trials and regulatory workLearning-focused culture and career growth opportunities

Role & Responsibilities • Receive, prepare, and submit Individual Case Safety Reports (ICSRs) to global regulatory authorities • Ensure all safety reports comply with country legislation and regulatory timelines • Lead large-scale safety reporting projects and monitor submission performance • Contribute to the development and continuous improvement of SOPs and procedural documents • Collaborate with internal teams on safety reporting activities • Act as the primary point of contact for safety reporting projects • Mentor and guide new team members and junior colleagues • Produce safety metrics and support limited financial project activities • Participate in internal and external meetings related to pharmacovigilance operations Qualification • Bachelor’s degree in Pharmacy, Life Sciences, or a related discipline Experience • Minimum 2+ years of experience in safety reporting or pharmacovigilance • Strong understanding of global safety reporting requirements • Proven skills in ICSR submissions, regulatory timelines, and safety reporting processes Skills • Global safety reporting and pharmacovigilance compliance • ICSR submission and regulatory timelines management • SOP development and cross-functional collaboration • Proficiency in Microsoft Office and safety databases • Strong attention to detail and multi-tasking ability • Ability to influence and collaborate across teams Benefits & Work Environment • Fully remote work model • Standard Monday–Friday schedule • Exposure to global pharmacovigilance projects • Opportunity to work with senior international stakeholders • Career growth in a regulated, high-impact safety environment About the Company • Thermo Fisher Scientific is a leading global life sciences organization, providing innovative solutions and cutting-edge technology in the fields of biotechnology, life sciences, and drug safety.

Role & Responsibilities • Assist in the coordination and administration of clinical trials • Ensure compliance with study protocols and regulatory requirements • Maintain and organize clinical trial documentation and regulatory submissions • Support preparation of study-related materials such as informed consent forms and case report forms • Collaborate with cross-functional teams for smooth trial execution • Track and report clinical trial metrics and milestones to management Qualification • Bachelor’s degree in Life Sciences, Pharmacy, or healthcare-related field Experience • Freshers or candidates with prior experience in clinical trials Skills • Strong understanding of GCP guidelines and clinical trial processes • Excellent organizational, communication, and multitasking skills • Ability to work in a fast-paced, collaborative environmentPerks & Benefits • Comprehensive health insurance plans for employees and families • Competitive retirement and savings plans • Generous annual leave and flexible working options • Global Employee Assistance Program (TELUS Health) • Country-specific benefits (gym memberships, travel passes, childcare vouchers) • Inclusive workplace fostering diversity, equity, and belonging About the Company • ICON plc, a global leader in healthcare intelligence and clinical research • Provides cutting-edge solutions in clinical development • Offers a supportive and inclusive workplace focused on career growth

Role & Responsibilities • Build and maintain scientific relationships with Key Opinion Leaders (KOLs), physicians and       healthcare professionals • Provide accurate, balanced and up-to-date scientific information on company products and    disease areas • Execute Medical Affairs plans for assigned therapeutic areas • Conduct scientific discussions, CMEs, advisory boards and medical education programs • Support clinical research activities and investigator-initiated studies • Collect and communicate field medical insights to internal teams • Support development and review of scientific and medical communication materials • Ensure compliance with regulatory, ethical and company policies during all field       activities • Represent Medical Affairs in internal cross-functional meetings Qualification • MBBS / MD / M.Pharm / PharmD / PhD in Life Sciences or related discipline Experience • 1–3 years of experience in Medical Affairs / Clinical Research / MSL role preferred Skills • Strong scientific and therapeutic area knowledge • Excellent presentation, communication and interpersonal skills • Ability to work independently in a field-based role • Good understanding of clinical research and regulatory guidelines • Willingness to travel within assigned territory About the Company • A leading pharmaceutical organization committed to developing innovative medicines and improving patient outcomes • Focused on delivering high-quality, patient-centric healthcare solutions across therapeutic areas

Role & Responsibilities • Manage HEOR project portfolios aligned with HORPs • Drive integrated budget planning and quarterly forecasting • Track milestones, timelines, scope and compliance • Coordinate cross-functional HEOR execution • Support contracting, procurement and sourcing activities • Facilitate change control and risk mitigation • Provide leadership updates and portfolio reporting • Represent HEOR in critical chain planning • Lead retrospectives and process improvements Qualification • Bachelor’s / Master’s in Pharmacy, Life Sciences, Science OR MBA Experience • 7–10 years in Pharma / HEOR / RWE / Clinical Project Management Skills • Portfolio & program management • Budgeting and forecasting • Stakeholder coordination • Risk & change management • MS Word, Excel, PowerPoint, MS Project • Strong analytical & communication skills About the Company • Eli Lilly and Company is a global healthcare leader delivering life-changing medicines and advancing patient access worldwide

Role & Responsibilities • Provide in-person clinical consultations at primary health centres • Deliver teleconsultation via voice, video and chat • Diagnose and treat patients using standard clinical protocols • Prescribe treatment, counsel patients and refer when required • Maintain patient confidentiality and accurate medical records • Document medical histories, examination findings and reports • Participate in health camps at community and corporate levels • Ensure compliance with quality, safety and company policies • Stay updated with medical developments and treatment guidelinesQualification • MBBS degree • MCI / State Medical Council registration mandatoryExperience • Minimum 1+ year of clinical experienceSkills • Strong communication and listening skills • Empathetic and patient-centric approach • Multilingual – Hindi, English mandatory • Conversational Kannada required • Comfortable with split day shift • Good documentation and telemedicine handling skillsAbout the Company Clinikk is a health-tech company transforming primary healthcare for middle-income families in India. It combines affordable health insurance with protocol-based primary care to serve over 600 million uninsured Indians, backed by leading investors including Rajan Anandan, 500 Startups and Times Internet.

Role & Responsibilities Conduct post-discharge follow-up teleconsultations Monitor recovery progress and identify early warning signs Assess medication, laboratory, diet and physiotherapy adherence Provide evidence-based clinical guidance (non-prescribing) Escalate high-risk cases to the clinical team Educate patients on lifestyle modifications and self-care practices Coordinate referrals, diagnostic services and allied healthcare support Maintain accurate electronic medical records Collaborate with program managers to improve care delivery models Qualification MBBS (Mandatory) Additional certification in Family Medicine or Public Health is an advantage Experience 2–4 years of clinical practice preferred Family Medicine, Internal Medicine, Emergency or Community Health experience desirable Skills Strong clinical judgment and analytical ability Excellent communication and patient counselling skills Knowledge of post-hospitalization recovery protocols Ability to prevent readmissions through early intervention Familiarity with teleconsultation platforms preferred Benefits Fixed daytime working hours Permanent employment Exposure to digital healthcare and population health programs Career growth in HealthTech and Value-Based Care systemsAbout the Company HEAPS Health Solutions is a health-tech organization headquartered in Bangalore with offices in Mumbai, Hyderabad and Delhi. The company leverages data analytics, artificial intelligence and machine learning to deliver value-based digital healthcare and patient care coordination services.

About Role & Responsibilities • Lead delivery operations for pharmacovigilance and drug safety services • Ensure adherence to global pharmacovigilance standards and timelines • Collaborate with teams to manage client relationships and regulatory compliance Qualification • B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences Experience • 3+ years in pharmacovigilance or related operations roles Skills • Leadership and team management skills • In-depth knowledge of pharmacovigilance processes and regulations About the Company Arcolab is a leader in pharmacovigilance and drug safety services, offering comprehensive solutions to the pharmaceutical industry

About Role & Responsibilities • Conduct health economics and outcomes research (HEOR) in the field of ophthalmology • Perform data analysis, including statistical modeling and cost-effectiveness analysis • Communicate results to stakeholders and support decision-making processes Qualification • Master’s degree or higher in Epidemiology, Biostatistics, Health Economics, Public Health, or related field Experience • 2+ years of experience in HEOR or related data analysis Skills • Strong background in data analysis and statistical techniques • Proficiency in programming languages such as SAS, R, or Python About the Company Alcon Laboratories is a global leader in eye care, providing innovative products and services to improve vision

About role & responsibilities • Perform advanced medical coding of diagnoses, procedures and medications • Code clinical trial data using MedDRA and WHO Drug dictionaries • Ensure accuracy, consistency and regulatory compliance across studies • Resolve complex coding discrepancies and medical queries • Collaborate with clinical, safety and data management teams • Support development and refinement of medical coding SOPs and conventions • Stay updated with global medical coding standards Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Healthcare or related field Skills • Strong working knowledge of MedDRA and WHO Drug • Understanding of clinical trial processes and regulatory requirements • High attention to detail and analytical problem-solving skills • Ability to work in cross-functional global teams • Good documentation and communication skills Experience • Proven experience in medical coding within clinical research Salary • ₹6,00,000 – ₹10,00,000 per annum (estimated) Benefits • Comprehensive health insurance for employee and family • Competitive leave entitlements • Retirement and long-term savings plans • Employee Assistance Programme (24/7 wellbeing support) • Life insurance coverage • Flexible benefits – childcare support, gym discounts, travel subsidies and health assessments • Hybrid / office-with-flex work model About the company • ICON plc is a global leader in healthcare intelligence and clinical research • Provides global clinical trial, regulatory and medical coding solutions

About Role & Responsibilities • Review central lab and imaging data • Support data analytics and reporting • Maintain quality control of trial data • Coordinate with global study teams • Ensure protocol and regulatory compliance Qualification B.Pharm / M.Pharm / Pharm.D Experience 1 – 4 years Skills • Clinical data management • Centralized monitoring • Regulatory documentation • Reporting tools & analytics About the Company ICON is a leading global CRO delivering high-quality clinical research services worldwide

About the role & responsibilities • Act as subject matter expert for Clinical Data Management across global clinical trials • Review clinical protocols, CRF design, CDASH and CDISC compliance • Lead database design, edit checks, listings, dashboards and reconciliation plans • Manage CDM project timelines, deliverables, budgets and client coordination • Ensure SOP, GCDMP and regulatory compliance across studies • Maintain audit-ready TMF and CDM documentation • Mentor CDM teams and develop training and best-practice materials • Drive process improvement, SOP updates and adoption of new CDM technologies Qualification • Graduate degree in Life Sciences / Pharmacy / Biotechnology / Clinical Sciences Experience • 8+ years in Clinical Data Management • Minimum 4 years in a Senior CDM role in CRO or pharma Skills • EDC systems and database validation • CDISC standards (CDASH, SDTM) • Data reconciliation and inspection readiness • TMF, GCDMP and regulatory compliance • Client and stakeholder management • Team leadership and mentoring About the company • Novotech is a leading global CRO delivering end-to-end clinical trial services across multiple therapeutic areas

Role & Responsibilities • Build and maintain strong scientific relationships with Key Opinion Leaders (KOLs), doctors, and healthcare professionals within the assigned territory • Conduct peer-to-peer scientific discussions on clinical evidence, disease management, and product value • Present research data, real-world evidence, and medical insights in a compliant and professional manner • Capture actionable medical insights, field feedback, and unmet clinical needs and share with internal teams • Support scientific activities such as CMEs, RTMs, advisory boards, and educational programs • Work independently in the field with 0% office involvement • Manage 50% city travel and 50% outstation travel within the assigned region • Collaborate with internal medical, sales, and strategy teams to support medical initiativesQualification • BDS preferred • BDS + MHA highly preferred • Pharm D candidates must have prior field experience Experience • Prior field-based experience is mandatory for Pharm D candidates • Fresh or experienced BDS candidates with strong scientific aptitude can be considered Skills • Strong scientific understanding and ability to interpret clinical data • Excellent communication and presentation skills • Ability to engage doctors in meaningful scientific conversations • Self-driven, independent, and comfortable with extensive travel • High ethical standards and compliance orientation• Chennai – Tamil language mandatory • Bangalore – Kannada language mandatoryWork Model • 0% office • 100% field-based • 50% city travel + 50% outstation travel About the Company • Dozee is India’s leading AI-based, contactless Remote Patient Monitoring (RPM) and Early Warning System (EWS), World’s first non-contact blood pressure monitoring technology.

Role & Responsibilities • Build and maintain strong scientific relationships with Key Opinion Leaders (KOLs), doctors, and healthcare professionals within the assigned territory • Conduct peer-to-peer scientific discussions on clinical evidence, disease management, and product value • Present research data, real-world evidence, and medical insights in a compliant and professional manner • Capture actionable medical insights, field feedback, and unmet clinical needs and share with internal teams • Support scientific activities such as CMEs, RTMs, advisory boards, and educational programs • Work independently in the field with 0% office involvement • Manage 50% city travel and 50% outstation travel within the assigned region • Collaborate with internal medical, sales, and strategy teams to support medical initiativesQualification • BDS preferred • BDS + MHA highly preferred • Pharm D candidates must have prior field experienceVacancies no - 03 Experience • Prior field-based experience is mandatory for Pharm D candidates • Fresh or experienced BDS candidates with strong scientific aptitude can be considered Skills • Strong scientific understanding and ability to interpret clinical data • Excellent communication and presentation skills • Ability to engage doctors in meaningful scientific conversations • Self-driven, independent, and comfortable with extensive travel • High ethical standards and compliance orientation• Chennai – Tamil language mandatory • Bangalore – Kannada language mandatoryWork Model • 0% office • 100% field-based • 50% city travel + 50% outstation travel About the Company • Dozee is India’s leading AI-based, contactless Remote Patient Monitoring (RPM) and Early Warning System (EWS), World’s first non-contact blood pressure monitoring technology.

Experienced dentist required for routine procedures, root canals, and cosmetic dentistry.

Experienced dentist required for routine procedures, root canals, and cosmetic dentistry.

Experienced dentist required for routine procedures, root canals, and cosmetic dentistry.

Role & Responsibilities: • Check medical admissibility of claims by validating diagnosis and treatment details • Scrutinize claims in accordance with insurance policy terms and conditions • Interpret ICD coding and assess co-pay, non-medical expenses, room rent capping, and tariff applicability • Differentiate between open billing and package billing • Understand and process PA and RI claims as per defined guidelines • Verify completeness of documents and raise IRs in case of insufficiency • Approve or deny claims within stipulated TAT • Handle escalations and respond to emails and internal queries Qualification: • MBBS or equivalent medical qualification preferred • Graduates with relevant claims or healthcare domain knowledge may be considered Experience: • 0–3 years of experience in medical claims processing, insurance, TPA, or healthcare operations Skills: • Medical Claims Processing & Adjudication • ICD Coding Interpretation • Analytical & Decision-Making Skills • Basic Computer & Typing Skills • Good Communication & Email Handling Skills • Attention to Detail & Time Management About the Company: • The organization operates in the healthcare insurance and TPA domain, providing end-to-end medical claims management services with a strong focus on accuracy, compliance, and timely settlements.