Bangalore Healthcare Jobs

Role & Responsibilities • Drive sales and promotion of Interventional Cardiology products within assigned territory • Achieve monthly, quarterly, and annual sales targets as per company goals • Develop new accounts and expand product usage in existing hospital accounts • Plan and execute territory sales strategies based on market, competition, and pricing analysis • Conduct regular sales calls with cardiologists, surgeons, and hospital stakeholders • Observe procedures in cath labs, EP labs, and operating rooms to support clinical usage • Build strong relationships with physicians, purchasing teams, and key decision-makers • Deliver product presentations, demonstrations, and clinical education programs • Address customer queries, complaints, and service issues with effective solutions • Coordinate with internal teams (clinical, marketing, pricing) for optimal account support • Ensure strict compliance with quality systems, patient safety, and company policies • Mentor and guide junior team members when requiredQualification • Graduate in Science / Pharmacy / Biomedical / Engineering or related discipline • MBA or relevant sales qualification preferredExperience • Mandatory experience in the medical device industry • Experience in Interventional Cardiology preferred • Exposure to Cardiology, Neurology, Endoscopy, Peripheral Intervention, Vascular Surgery, or CRM is an advantage Skills • Strong sales, negotiation, and relationship-building skills • Good understanding of interventional cardiology procedures and devices • Ability to analyze sales data and develop actionable plans • Excellent communication and presentation skills • Strong customer-centric and result-driven mindset • Ability to work independently in a field-based role • Sound judgment, problem-solving, and decision-making abilitiesAbout Company • Boston Scientific is a global leader in medical devices with 40+ years of innovation , Dedicated to advancing science for life and improving patient outcomes

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

Roles & Responsibilities • Process Individual Case Safety Reports (ICSRs) in compliance with global pharmacovigilance regulations • Perform case intake, triage, data entry, narrative writing, and medical coding using MedDRA and WHO-DD • Ensure adherence to ICH-GCP, ICH-E2A/E2B, and other global regulatory guidelines • Conduct quality checks and ensure timely submission of safety cases to regulatory authorities • Support ongoing safety surveillance and signal detection activities • Maintain accurate documentation and ensure inspection and audit readiness • Collaborate with cross-functional pharmacovigilance and regulatory teams Qualification • B.Pharm / M.Pharm / Pharm D from a recognized institution • Mandatory valid Pharmacy License Experience • Minimum 1 year of hands-on experience in pharmacovigilance or drug safety operations • Experience in ICSR processing and global safety reporting preferred Skills • Strong knowledge of pharmacovigilance regulations and case processing workflows • Hands-on experience with MedDRA and WHO-DD coding • High attention to detail and quality mindset • Good written and verbal communication skills • Ability to work collaboratively in a global, compliance-driven environment • Willingness to relocate to Bangalore or Mysore after 6 months About the company Qinecsa is a global life sciences and healthcare services organization specializing in pharmacovigilance, regulatory affairs, and clinical safety solutions, supporting pharmaceutical and biotech companies worldwide with high-quality, compliant, and patient-focused drug safety services while offering strong career growth opportunities in a global work environment.

Roles & Responsibilities • Recruit and enroll eligible study participants as per approved protocols • Coordinate patient visits, procedures, follow-ups, and study schedules • Enter, review, and maintain accurate clinical data in EDC systems • Act as primary point of contact for study participants and address protocol-related queries • Ensure compliance with ICH-GCP, ethical guidelines, and regulatory requirements • Prepare, maintain, and update essential study documents and trial files • Manage proper filing and archival of CRFs and study-related documentation • Coordinate with sponsors, ethics committees, investigators, and multiple study sites • Support Principal Investigators (PI) for smooth conduct of clinical studies Qualification • Bachelor’s or Master’s degree in Biotechnology, Biochemistry, Microbiology, Life Sciences, Nursing, Pharmacy, or related discipline • Diploma in Clinical Research is an added advantage Experience • 1-5 years of experience in clinical research coordination or site operations • Hospital-based or site-level research experience preferred Skills • Strong knowledge of clinical trial processes and documentation • Working understanding of ICH-GCP and regulatory requirements • Good data management, organizational, and planning skills • Proficiency in MS Word and MS Excel • Strong communication and interpersonal skills • Ability to coordinate with multiple stakeholders and sites About the Company Indira IVF Hospital is one of India’s leading fertility and reproductive healthcare organizations, known for its extensive national presence, patient-centric approach, and commitment to clinical excellence, research, and ethical medical practices in assisted reproductive technologies.

Role & Responsibilities • Review patient adverse events and medical data in pharmacovigilance databases. • Assess drug safety, causality, and potential risks. • Perform medical review of ICSRs and support safety evaluations. Qualifications • MBBS or MD only. Experience • 1–6 years of experience as a Medical Reviewer in Pharmacovigilance. Skills • Strong understanding of drug safety and adverse event assessment. • Attention to detail and regulatory compliance knowledge. About the Company • India’s 2nd largest KPO in the Life Sciences & Healthcare domain.

Roles & Responsibilities:• Communicate effectively with the clinical and front-desk team to ensure smooth patient flow• Maintain clear, empathetic, and professional patient communication throughout every treatment• Provide accurate diagnoses and explain treatment plans in simple, reassuring language• Collaborate with the team to ensure clarity in diagnosis, coordination, and follow-ups• Uphold Dental Tribe’s standards of patient care, hygiene, and ethical practiceQualifications:• Bachelor of Dental Surgery (BDS) from a recognized institution• Proficiency in Root Canal Treatment (minimum 2 years required)• Skilled in fillings, basic extractions, restorative, and preventive procedures• Knowledge of Hindi and English; willingness to learn basic Kannada for smoother patient communicationExperience:• Minimum 2 years of clinical experienceKey Skills:• Root Canal Treatment (RCT)• Fillings and basic extractions• Restorative and preventive dental procedures• Diagnosis and treatment planning• Patient care and communicationAbout the Company:Dental Tribe is one of the most referred dental service destinations, dedicated to providing patient-centric, high-quality dental care. The clinic emphasizes ethical practice, modern technology, and a collaborative environment to ensure exceptional outcomes and patient satisfaction.

Roles & Responsibilities • Support timely global product launches for the Life Science business • Ensure compliance with global chemical regulations including GHS, SDS, chemical registration, and trade compliance • Collect, analyze, and validate product composition and physical property data • Review product formulations and hazard classification documentation • Collaborate with Product Management, internal regulatory teams, and external vendors • Coordinate with third-party vendors to ensure accuracy and completeness of regulatory data • Use SAP, JIRA, Palantir, and MS Office tools for regulatory data processing and tracking • Provide validated regulatory inputs to downstream compliance and processing teams Qualification • Master’s degree in Chemistry, Biochemistry, Toxicology, or Pharmacy Experience • Experience or academic exposure to regulatory affairs, chemical compliance, or product safety preferred • Familiarity with global regulatory frameworks is an advantage Skills • Understanding of chemical composition and hazardous characterization • Knowledge of GHS, SDS, and chemical regulatory compliance concepts • Data analysis, validation, and critical thinking skills • Experience with SAP, JIRA, and Palantir preferred • Strong communication, documentation, and vendor coordination abilities • Detail-oriented, collaborative, and quality-focused approach About the Company Merck is a global leader in Healthcare, Life Science, and Electronics, operating across multiple international markets. The company is known for its strong focus on innovation, regulatory excellence, sustainability, and inclusive work culture. Merck offers professionals the opportunity to work on globally impactful products while building a long-term career in regulatory affairs and life sciences.

Roles & Responsibilities • Support Lead Data Manager and act as backup for end-to-end CDM activities • Perform CRF review, specifications development, and database build/UAT support • Conduct clinical data review, query management, and line listing reviews • Perform medical coding and AE/SAE reconciliation • Maintain data management documentation with version control • Coordinate with EDC vendors and third-party stakeholders • Support database lock, metrics reporting, and process improvements • Train study teams on CRF, EDC, and study-specific processes Qualification • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Computer Applications, or related discipline Experience • Relevant experience in Clinical Data Management within a CRO or sponsor setup • Hands-on experience across the clinical trial lifecycle Skills • Strong experience with EDC systems (Medidata Rave, Veeva Vault preferred) • Good knowledge of ICH-GCP and clinical trial processes • Experience in medical coding, data review, and database lock • Strong analytical, documentation, and communication skills About the Company Precision For Medicine is a global CRO focused on precision medicine and advanced clinical research, delivering innovative data-driven solutions to accelerate drug development across complex and rare diseases.

Roles & Responsibilities • Perform clinical data review, query management, and discrepancy resolution • Support DMP development, data review guidelines, and database setup/lock • Execute reconciliations, listings, and data quality checks • Maintain data management documentation and eTMF records • Generate study status reports and support project meetings • Train junior team members and act as backup to the CDM Qualification • Bachelor’s or Master’s degree in Life Sciences, Health Sciences, IT, or related field Experience • 3-4 years in clinical research • Clinical Data Management experience preferred • Experience in global, cross-functional teams Skills • Strong knowledge of CDM processes, GCP, and medical terminology • Good analytical, communication, and organizational skills • Ability to work independently in a remote setup About the Company Fortrea is a global CRO providing end-to-end clinical development services, known for high-quality data delivery, innovation, and flexible work environments for clinical research professionals.

Roles & Responsibilities • Author and review regulatory medical writing documents including Clinical Study Reports (CSRs), protocols, Investigator’s Brochures (IBs), Informed Consent Forms (ICFs), and submission documents • Act as lead writer or submission coordinator for assigned projects • Manage and coordinate contributions from multiple writers across related deliverables • Serve as the primary point of contact for clients, ensuring clear communication and timely delivery • Drive process improvements and contribute to development of medical writing best practices • Mentor, train, and technically guide junior medical writers • Support business development activities by contributing to proposals and client interactions Qualification • Bachelor’s or advanced degree in Life Sciences, Healthcare, Pharmacy, or related discipline Experience • Minimum 6+ years of experience in regulatory medical writing • Proven expertise in authoring key clinical and regulatory documents • Experience across multiple therapeutic areas including vaccines, immunology, oncology, cardiovascular, neurology, infectious diseases, endocrine, gastrointestinal, autoimmune, and mental health Skills • Strong scientific, analytical, and regulatory writing skills • Excellent communication and stakeholder management abilities • Ability to lead projects independently and manage multiple timelines • High attention to detail with strong quality and compliance focus • Capability to work under pressure and manage variable workloads About the Company VUEVERSE is a specialized medical communications and regulatory writing organization delivering high-quality, compliant scientific and regulatory content to pharmaceutical and CRO clients across global markets, with a strong focus on expertise, innovation, and mentorship.

Roles & Responsibilities • Manage electronic Trial Master File (eTMF) activities including Trial, Country, and Site artifacts in line with TMF processes • Classify, review, and process documents through Smart Inbox and perform ARC reviews • Conduct visual quality checks to ensure document clarity, readability, and completeness • Perform Audit Ready Checks to maintain inspection-ready eTMF at all study stages • Track, process, and maintain final essential documents across the clinical study lifecycle • Ensure compliance with company SOPs, sponsor SOPs, GCP, ICH, and regulatory requirements • Support QA and sponsor audits, identify issues, and implement corrective and preventive actions • Collaborate with Business Process, Study, and cross-functional teams to meet project and client expectations • Participate in internal and external study meetings as required • Contribute to continuous improvement initiatives to enhance quality, productivity, and processes Qualification • Bachelor’s Degree in Life Sciences or Business • Master’s Degree in Life Sciences or Business preferred Experience • 6-12 months of experience in a clinical research environment • Equivalent clinical research experience may be considered Skills • Strong understanding of GCP, ICH guidelines, and regulatory documentation requirements • Proficiency in Microsoft Office, web-based applications, and Adobe Acrobat • Familiarity with clinical electronic systems is an advantage • Excellent communication, interpersonal, and organizational skills • High attention to detail and ability to manage multiple tasks About the Company Fortrea is a leading global Contract Research Organization dedicated to advancing clinical development through innovation, collaboration, and scientific excellence, helping transform lives by delivering high-quality clinical trials worldwide.

Roles & Responsibilities • Support the business process owner for literature surveillance activities • Manage training documentation and user access for literature surveillance and reconciliation systems • Perform operational activities including literature reconciliation, quality control of non-ICSR literature, and article uploads • Conduct ICSR reconciliation, quality monitoring, and safety spot checks in collaboration with cross-functional teams • Handle team mailboxes and ensure timely action on all pharmacovigilance communications • Ensure end-to-end compliance with global pharmacovigilance regulations across the literature surveillance lifecycle Qualification • B.Pharm / M.Pharm / Pharm.D / MSc / BSc / Life Sciences / Medicine Experience • Minimum 3 years of experience in a pharmacovigilance environment • Proven experience in literature safety surveillance and ICSR reconciliation • Exposure to global drug safety regulations for clinical and post-marketing products Skills • Strong knowledge of global pharmacovigilance regulations and safety reporting requirements • Hands-on experience with literature surveillance and reconciliation processes • Experience with ArisG Safety Database (preferred) • Excellent written and verbal communication skills • Ability to work effectively in a global, cross-functional matrix environment About the Company Merck is a global science and technology leader operating across healthcare, life science, and electronics, committed to innovation, patient safety, and advancing human health through cutting-edge research and global collaboration.

Roles & Responsibilities • Manage clinical study documents in line with client, regulatory, and ICON requirements • Perform document receipt, review, quality checks, scanning, indexing, filing, and archiving in the Trial Master File (TMF) • Ensure continuous compliance with ICON SOPs, work procedures, and applicable regulatory guidelines • Collaborate with study teams, clients, and internal ICON departments to support study deliverables • Participate in internal and external audits and support inspection readiness activities • Prepare and maintain TMF status reports and tracking logs • Identify gaps or issues in TMF documentation and support corrective actions • Participate in training programs to enhance TMF and clinical research knowledge • Support special projects and additional responsibilities as assigned by the Manager Qualification • B.Pharm / M.Pharm / Pharm.D / BSc / MSc in Life Sciences or related disciplines Experience • 1-15 years of experience in TMF management or clinical document management • Strong understanding of clinical trial documentation and TMF processes Skills • Strong oral and written communication skills • Excellent attention to detail and document accuracy • Good interpersonal and stakeholder coordination skills • Strong organizational and time management abilities • Working knowledge of clinical trial regulations and documentation standards About the Company ICON plc is a global leader in clinical research and healthcare intelligence, committed to advancing clinical development through innovation, partnership, and integrity, while fostering an inclusive work environment focused on improving patient lives worldwide.

Roles & Responsibilities• Assess patients and evaluate physiotherapy and rehabilitation needs• Design and implement personalized physiotherapy treatment plans• Provide treatment for musculoskeletal, neurological, and post-operative conditions• Conduct therapeutic exercises and physiotherapy interventions• Educate patients on exercises, posture correction, and injury prevention• Monitor patient progress and update treatment plans accordingly• Maintain accurate treatment records and follow clinical protocols• Build trust and maintain long-term relationships with patientsQualifications• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT) from a recognized institutionExperience• Experienced candidates preferred• Freshers with strong clinical knowledge may also be consideredSkills• Strong patient assessment and treatment planning skills• Knowledge of rehabilitation and physiotherapy techniques• Good communication skills in English• Patient-focused and empathetic approach• Ability to work independently in a clinic setting• Willingness to learn and grow with the clinicWhat We Offer• Free accommodation provided• Supportive and professional work environment• Opportunity to grow with a newly launched and expanding clinic• Stable role within a premium gated residential communityAbout the CompanyAdvanced Wellness Clinic is a patient-focused physiotherapy and wellness center based in Sarjapur, Bangalore, dedicated to delivering high-quality, personalized care exclusively within premium gated communities. The clinic emphasizes holistic rehabilitation, professional ethics, and long-term patient well-being through structured and compassionate physiotherapy services.

Roles & Responsibilities • Lead end-to-end Clinical Data Management (CDM) activities for single or multi-service clinical studies • Gather and analyze study setup requirements in collaboration with sponsors and internal stakeholders • Oversee data collection, data cleaning, validation, and database lock activities • Validate and manage new device and system integrations with minimal supervision • Ensure all study deliverables meet sponsor expectations, quality standards, and timelines • Track project progress, identify risks and issues, and implement corrective and preventive actions • Lead study kick-off meetings, internal team meetings, and sponsor audits • Support onboarding and training of new team members • Collaborate with programming and technology teams to drive automation and process improvements • Contribute to the development, review, and maintenance of SOPs and work instructions Qualification • B.Pharm / M.Pharm / Pharm.D / BSc / MSc in Life Sciences, Health Sciences, Clinical, Biological, Mathematical Sciences, or related discipline Experience • 3-4 years of clinical data management experience • Minimum 1 year of experience as a CDM Project Lead preferred Skills • Strong understanding of the drug development lifecycle and overall clinical research process • Hands-on expertise in clinical data collection, validation, and reporting • Proficiency in Microsoft Excel, Word, and Outlook • Strong spoken and written English communication skills • Good leadership, problem-solving, and stakeholder management skills • Ability to manage multiple priorities and meet project timelines About the Company IQVIA is a global leader in clinical research, healthcare analytics, and life sciences intelligence, supporting pharmaceutical, biotechnology, and healthcare organizations worldwide through advanced analytics, technology-enabled solutions, and deep scientific expertise to improve patient outcomes and accelerate innovation.

Roles & Responsibilities • Prepare, review, and submit high-quality regulatory filings (pre- and post-approval) for US FDA–regulated complex generic products including inhalation, ophthalmic, implant, and drug–device combinations • Manage original applications, amendments, deficiency responses (IRs, DRLs, CRLs), and post-approval supplements • Evaluate change controls and determine appropriate regulatory pathways (PAS, CBE-30, CBE-0, AR) in coordination with regulatory management • Compile and submit post-approval changes in compliance with FDA, ICH guidelines, and internal SOPs • Support early FDA engagement to align development strategies and reduce regulatory risks • Act as a regulatory point of contact for cross-functional teams (R&D, QA, Manufacturing, Packaging, DMF holders) as needed • Monitor regulatory timelines, identify documentation gaps, and ensure “Right-First-Time” submissions • Track regulatory intelligence and monitor FDA databases such as Drugs@FDA and Orange Book • Participate in audits, inspections, and continuous process improvement initiatives Qualifications • Master’s degree in Pharmacy with specialization in Regulatory Affairs / Quality Assurance preferred Experience • Minimum 4+ years of pharmaceutical industry experience • Hands-on experience with complex generics such as inhalation, ophthalmic, implant, or drug–device combination products preferred Skills • Strong knowledge of US FDA and ICH regulatory guidelines • Experience in regulatory submissions and post-approval change management • Excellent written and verbal communication skills • Strong organizational skills with attention to detail and multitasking ability • Analytical, critical, and logical thinking skills • Ability to work independently and collaboratively across cross-functional teams About the Company Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating in nearly 60 countries. Driven by a mission to make healthcare more affordable and accessible, Teva supports over 200 million patients worldwide every day through high-quality medicines, innovation, and a strong commitment to diversity, inclusion, and ethical practices.

Role & Responsibilities• Conduct personalized 1-on-1 physiotherapy sessions at client homes• Perform initial assessments and functional movement screenings• Develop and implement customized rehab protocols for musculoskeletal and age-related conditions• Focus on mobility, posture correction, pain management, balance, and fall prevention• Maintain client session records, monitor progress, and adjust treatment plans• Collaborate with fitness coaches, nutritionists, and internal teams for holistic care• Educate clients and families on corrective exercises, ergonomics, and preventive practicesQualifications• BPT or MPT degree from a recognized institutionExperience• Minimum 1–3 years of clinical or on-field physiotherapy experience (senior-focused experience preferred)Skills Required• Strong understanding of functional movement therapy and rehab protocols• Empathetic, patient-centered approach with excellent communication skills• Ability to build trust with senior clients• Valid driving license and access to a two-wheeler for home visits• Organized, proactive, and able to work independentlyAbout the CompanyKineticAge is a fast-growing wellness brand transforming the lives of adults aged 50+ through home-based physiotherapy, fitness, and rehab-focused care. The company emphasizes personalized, evidence-based interventions to improve mobility, strength, and overall wellness in seniors, while fostering a collaborative and growth-oriented work environment.

Role & Responsibilities• Deliver preventive, diagnostic, and therapeutic dental care during home visits and corporate dental camps• Perform routine general dentistry procedures independently• Manage patients professionally in field-based settings• Ensure patient comfort and clear communication throughout treatment• Educate patients on oral hygiene, preventive care, and long-term dental health• Maintain accurate clinical records and treatment documentation• Follow strict infection control, safety, and clinical protocolsQualifications• BDS from a recognized dental institution• Valid State Dental Council registrationExperience• Minimum 1+ year of clinical experience• Experience in preventive and diagnostic dentistry preferredSkills Required• Strong knowledge of general dentistry procedures• Excellent patient-handling and communication skills• Ability to work independently during field visits• High standards of hygiene, sterilization, and clinical safety• Compassionate, responsible, and adaptable approach to careAbout the CompanyCura Care, Bangalore is a rapidly growing healthcare platform delivering accessible and patient-centric medical and dental services through home visits and corporate health camps. Focused on preventive care and clinical excellence, Cura Care aims to make quality healthcare convenient, ethical, and impactful across urban communities.

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) • Ensure medical accuracy, completeness, and regulatory compliance of safety cases • Apply clinical judgment for case assessment, seriousness, causality, and expectedness • Support global pharmacovigilance and regulatory reporting activities • Ensure adherence to GVP, ICH guidelines, and internal SOPs Qualifications & Experience • MBBS / MD with valid MCI registration • Minimum 1 year of hands-on experience in ICSR medical review Skills • Strong knowledge of pharmacovigilance and clinical terminology • Understanding of regulatory reporting requirements • Good analytical and documentation skills About the Company • Indegene is a global life sciences solutions provider delivering pharmacovigilance, medical affairs, and regulatory services across worldwide markets