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 1–20 of 20 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.
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.
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.
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.
AWS DevOps Engineer
Infosys Limited
Bangalore2-5 Years · Hybrid19 SeptJoin Infosys Limited as an AWS DevOps Engineer to aid consulting teams in designing, deploying, and supporting cloud solutions.
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.
Senior Application Software Engineer
Oracle
Bangalore2-5 Years · Hybrid13 SeptDesign and develop backend services and customer-facing features for a next-generation customer support ticketing platform.
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.
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.
KOL Engagement Specialist
Astellas
Bangalore2-5 Years · Hybrid11 SeptSupport compliant engagement with healthcare professionals and key external experts across congresses, events, funding, and grants while enabling efficient Medical Affairs operations.