Pharma, Clinical Research & Healthcare Jobs in India
511 open roles from pharma companies, CROs and hospitals, with new openings added most days. Apply directly through each employer's own page or contact.
Showing 1–25 of 28 jobs
Analyst Graphic Designer I – Medical Publications
AstraZeneca
Bengaluru2-5 Years · Hybrid2 days agoAstraZeneca is hiring an Analyst Graphic Designer I – Medical Publications in Bengaluru to create accurate, publication-ready visuals and layouts for scientific communications. The role is hybrid and calls for at least three years of regulated medical, healthcare or scientific publishing design experience.
Engagement Analyst – External Expert Engagement Services
AstraZeneca
Bengaluru2-5 Years · Hybrid30 SeptThe Engagement Analyst role within AstraZeneca's External Expert Engagement Services (E3S) sits at the intersection of Medical Affairs, Commercial and Compliance operations. Based at Manyata Tech Park, Bangalore, this individual-contributor position governs the end-to-end lifecycle of engagements with healthcare providers and patients — advisory boards, consulting assignments and speaking programmes that shape how AstraZeneca's medicines are understood, prescribed and adopted. Because every such engagement carries transparency and anti-bribery obligations, the analyst protects AstraZeneca's licence to operate while accelerating scientific exchange. For professionals with 1–5 years of experience in regulated contracting or compliance workflows, the role offers global exposure, direct partnership with Medical Affairs, Nominated Signatories and Legal, and a clear pathway into compliance, medical affairs operations or risk management careers.
Pharmacovigilance Reporting Associate
ICON
Bangalore2-5 Years · Remote30 SeptSupports accurate and timely preparation, review and submission of pharmacovigilance safety reports for clinical trials and post-marketing activities. The role combines safety-report preparation, adverse-event data analysis, regulatory compliance and cross-functional collaboration.
Senior Global Regulatory Scientist
ICON
Bangalore2-5 Years · Hybrid30 SeptSenior Global Regulatory Scientist responsible for leading global clinical-trial regulatory activities, submission strategy, regulatory project teams, client deliverables, and compliance across pharmaceutical clinical trials in India.
Medical Writer I / Medical Writer II
Parexel
Bangalore2-5 Years · Hybrid30 SeptDevelop high-quality pharmacovigilance and regulatory safety documents, conduct signal detection and assessment, synthesize scientific evidence, and support regulatory compliance across the product lifecycle.
Clinical Programmer I / II
AstraZeneca
Bengaluru2-5 Years · Hybrid29 SeptThe Clinical Programmer I/II role at AstraZeneca's Manyata Tech Park campus in Bangalore sits at the intersection of clinical science and software engineering — the precise place where modern drug development is being reinvented. Reporting into the Biometrics and Clinical Programming function, this individual-contributor position converts raw trial data from EDC and third-party vendors into validated datasets, automated quality checks and executive-ready dashboards that study teams use to spot anomalies weeks earlier. Because AstraZeneca's pipeline spans oncology, cardiovascular, respiratory and rare disease, the programmer's output directly shapes how quickly and confidently go/no-go decisions are made. For a technically strong SAS or Python developer who wants their code to carry patient-level consequence rather than purely commercial consequence, this is a rare hybrid of engineering craft, regulatory rigour and genuine therapeutic impact.
Senior Statistical Programmer
AstraZeneca
Bengaluru2-5 Years · Hybrid28 SeptBased at AstraZeneca's Manyata Tech Park campus in Bangalore, the Senior Statistical Programmer I role sits within the Oncology Biometrics Programming department—a critical function that turns raw clinical trial data into regulatory-ready evidence. As part of a global team dedicated to eliminating cancer as a cause of death, you will support and lead statistical programming activities across high-priority oncology studies, from clinical study report development to regulatory submissions and commercialisation. This is a compelling opportunity for an experienced SAS programmer who wants to see their code influence filings, accelerate patient access, and shape evidence-based decisions. AstraZeneca's deep pipeline, collaborative research culture, and investment in science and technology make this a career-defining platform for professionals who combine technical rigour with a passion for improving patient outcomes.
Senior Biostatistician
Iqvia
Bengaluru2-5 Years · Hybrid26 SeptThe Senior Biostatistician at IQVIA in Bengaluru is a strategic, client-facing role at the intersection of clinical trial design, regulatory-grade evidence, and advanced analytics. IQVIA supports pharmaceutical, biotechnology, and medical device sponsors across global programs, so this position directly influences how studies are powered, analyzed, and reported. The role owns statistical methods sections, analysis plans, datasets, and tables, listings, and figures (TLFs) while guiding junior staff and collaborating with data management, clinical, and programming teams. It is compelling for professionals who want to deepen expertise in CDISC, ICH-GCP, and modern trial methodology while gaining leadership exposure, budget accountability, and direct client interaction. It also offers a pathway into principal, team lead, or sponsor-side biostatistics roles in India’s rapidly expanding life-sciences market.
Senior Medical Writer
Gsk
Bengaluru2-5 Years · Onsite26 SeptGSK is a global biopharmaceutical leader focused on vaccines and specialty medicines across respiratory, immunology, oncology, HIV and infectious diseases. The Senior Medical Writer in Bengaluru sits within a high-impact R&D documentation function that translates complex clinical and regulatory data into clear, compliant submissions. This role directly supports protocols, clinical study reports, CTD modules, investigator brochures and health-authority responses, making it central to accelerating GSK's pipeline and patient access. Working in a global matrix with clinical leads, biostatisticians and asset teams, the writer ensures scientific integrity and timely delivery. For experienced medical writers, this is a compelling opportunity to deepen regulatory writing expertise, collaborate across therapeutic areas, and contribute to medicines and vaccines that impact billions. GSK's culture of ambition for patients, accountability and inclusion further makes this a strong career platform in India's fast-growing biopharma sector.
Area Medical Advisor - Hepatology
Gsk
Bengaluru2-5 Years · Hybrid25 SeptGSK’s Area Medical Advisor, Specialty, Hepatology is a field-facing Medical Affairs role based in Bengaluru, designed to be the scientific bridge between GSK’s hepatology portfolio and the external clinical community. You will translate complex clinical data into credible, on-label scientific exchange with Key External Experts, gastroenterologists, hepatologists and institutional stakeholders. As GSK advances specialty medicines and vaccines across respiratory, immunology, oncology, HIV and infectious diseases, hepatology remains a critical therapy area where medical evidence, real-world insights and compliant scientific engagement shape brand strategy and patient outcomes. This position offers a rare blend of clinical science, strategic influence and cross-functional leadership, ideal for a physician seeking to deepen therapeutic expertise, build KOL networks and influence the standard of care in liver disease across India.
Clinical Data Team Lead
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid25 SeptLead clinical data management activities for clinical research studies, coordinating data management teams, clients, project leads, documentation, training, metrics and study deliverables.
Kit Production Assistant III
Labcorp
Bangalore2-5 Years · Onsite24 SeptSupport clinical research kit inventory operations by maintaining project and site-level Kit Material Supply systems, processing work orders, resolving kit-supply issues, supporting investigator sites, and ensuring accurate documentation and timely service delivery.
Medical Data Reviewer
ICON
Bangalore2-5 Years · Remote23 SeptProvide expert medical oversight of clinical trial data, ensuring accuracy, consistency, and patient safety in a sponsor-dedicated model.
Clinical Data Coordinator II (CDC II)
ICON
Bangalore2-5 Years · Hybrid23 SeptDeliver high-quality clinical data management tasks, maintaining eCRFs, data validation specifications, and supporting study metrics.
Clinical Trial Manager
Astellas
Bangalore2-5 Years · Hybrid22 SeptClinical Trial Manager responsible for planning, setting up, and executing assigned clinical trials while coordinating cross-functional teams, vendors, investigators, sites, budgets, timelines, and trial deliverables in compliance with GCP, ICH, SOPs, and regulatory requirements.
Centralized Monitoring Analyst (Level I & II)
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid21 SeptCentralized Monitoring Analyst role supporting clinical trials through analysis of operational and patient data, identification of trends and risks, documentation of findings and centralized monitoring activities.
Manager, RA Publishing & Submissions
Astellas
Bangalore2-5 Years · Onsite19 SeptManager-level Regulatory Affairs Publishing & Submissions role focused on global regulatory submissions, publishing operations, submission standards, quality control and regulatory operations.
Safety Surveillance Adviser I
Novo Nordisk Global Business Services (GBS)
Bangalore2-5 Years · Onsite19 SeptSafety Surveillance Adviser I supporting Global Patient Safety activities across the lifecycle of Novo Nordisk medicines, including safety surveillance, signal and aggregate management, safety labelling, regulatory safety reporting, and cross-functional safety communication.
Senior CDA/ Clin Data Assoc II
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid18 SeptSenior Clinical Data Associate role supporting clinical data cleaning, database activities, query management, data review, study-specific processes, reporting, and training within a global clinical research organization.
Pharmacovigilance Reporting Associate
ICON
Bangalore2-5 Years · Hybrid17 SeptPrepare and review accurate, timely pharmacovigilance safety reports for clinical trials and post-marketing activities while ensuring regulatory compliance and effective cross-functional collaboration.
Safety Surveillance Adviser I
Novo Nordisk
Bangalore2-5 Years · Onsite16 SeptSafety Surveillance Adviser role within Global Patient Safety, supporting product safety surveillance, safety labelling, aggregate reporting, risk management and proactive safety communication across the medicine lifecycle.
CDC II
ICON
Bangalore2-5 Years · Hybrid13 SeptSupport clinical data management activities for clinical trials by maintaining eCRFs and validation specifications, reconciling clinical and third-party data, monitoring study metrics and resolving data issues. The role contributes to high-quality clinical data delivery within a global clinical research organisation.
Senior CDA/ Clin Data Assoc II
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid13 SeptPerform clinical data management and data cleaning activities for clinical trials while ensuring compliance with GCP, SOPs and client requirements, with responsibility for specialized processes and support to junior staff.
PK Medical Writer
ICON
Bangalore2-5 Years · Remote12 SeptDevelop and deliver high-quality Clinical Pharmacology & Pharmacometrics documents, including population PK/PD plans and reports, CSRs, protocols, and regulatory clinical documents. The role supports clinical research projects through scientific writing, document coordination, quality control, and cross-functional collaboration.
Clinical Trial Specialist
Astellas
Bangalore2-5 Years · Hybrid12 SeptSupport the end-to-end operational delivery of assigned clinical trials at Astellas, working with Clinical Trial Leads, Clinical Trial Managers, sites, CROs, vendors, and global cross-functional teams. The role focuses on quality, compliance, accurate trial execution, and operational excellence.