Pharma, Clinical Research & Healthcare Jobs in India
517 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 108 jobs
Medical Director, Patient Safety Physician
AstraZeneca
Bengaluru5+ Years · HybridTodayAstraZeneca's Medical Director, Patient Safety Physician role places a medically qualified safety leader at the centre of benefit-risk decision-making for high-impact therapies spanning late-stage development through post-marketing. Based in Bengaluru, the position owns the clinical safety strategy for assigned programmes, defining identified and potential risks, setting safety go/no-go criteria, and shaping risk-minimisation approaches that ultimately influence labelling and regulatory outcomes. Because AstraZeneca's pipeline stretches across oncology, cardiovascular, respiratory and rare disease, this is a rare opportunity to work on genuinely transformative medicines while collaborating with regulators, QPPVs and external partners. For physicians seeking to move beyond bedside practice into strategic pharmacovigilance leadership, it offers exceptional visibility, cross-cultural exposure and durable long-term career capital.
Associate Global Development Scientist Director I
AstraZeneca
Bangalore5+ Years · HybridYesterdayAstraZeneca is recruiting a senior clinical development scientist for its Bangalore site. The role supports late-phase clinical programmes across protocol work, data and safety review, publications and regulatory documents in a hybrid team setting.
Senior Manager - Publications Delivery Lead - Scientific Publications (GBS BBU)
AstraZeneca
Bengaluru5+ Years · HybridYesterdayAstraZeneca is recruiting a Publications Delivery Lead to set up and run a multi-tier scientific publications team staffed by content authors, visual designers and iEnvision specialists. The role pairs people leadership with operational governance, covering SOPs, delivery metrics, quality control and global collaborator management.
Analyst Graphic Designer I – Medical Publications
AstraZeneca
Bengaluru2-5 Years · HybridYesterdayAstraZeneca 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.
Statistical Science Director
AstraZeneca
Bengaluru5+ Years · Hybrid5 days agoAstraZeneca is hiring a Statistical Science Director in Bengaluru to lead statistical strategy across global medicine development, from early discovery through registration. The role owns statistical content for study designs, protocols, analysis plans and submissions, and represents statistical strategy at internal governance forums.
Principal Tech Engineer – Site Serialisation Systems
Gsk
Bengaluru5+ Years · Onsite5 days agoGSK is recruiting a Principal Tech Engineer to lead technical work on site serialisation systems within its PIMMS Manufacturing Track & Trace product. The position is hands-on, spanning solution design, validation, implementation and the resolution of complex integration failures across multiple manufacturing sites.
Director - SN Risk & Compliance Manager
Gsk
Bengaluru5+ Years · Onsite9 days agoGSK is hiring a Director - SN Risk & Compliance Manager in Bengaluru to hold the risk and compliance position of the ServiceNow and enterprise tools platform across its operational life. The role runs risk and compliance assessments on platform change, verifies control attestation before release, and maintains qualification and release evidence.
Senior Clinical Programmer II
AstraZeneca
Bengaluru5+ Years · Hybrid15 days agoAt AstraZeneca, the Senior Clinical Programmer II role sits within the Biometrics and Clinical Data Sciences function, powering the data-driven oversight of global trials in cardiovascular, renal, metabolic, respiratory, and immunology. This position is pivotal to turning complex clinical data into validated listings, dashboards, and actionable insights that accelerate trial decisions, improve data quality, and support regulatory submission readiness. The programmer partners with data management, clinical operations, biometrics, and study teams to build scalable programming solutions using SAS, Python, R, SQL, Power BI, and Spotfire. As an individual contributor and mentor, you will shape enterprise standards, reduce cycle times, and ensure inspection-ready outputs. This is a compelling career opportunity for an experienced clinical programmer who wants to blend deep technical mastery with patient-focused drug development at a top global pharmaceutical company.
Director, Patient Safety
AstraZeneca
Bengaluru5+ Years · Hybrid23 days agoAt AstraZeneca, the Director-Patient Safety role in Bangalore is a strategic leadership position within Global Patient Safety. It directly influences how innovative medicines progress from early development through lifecycle management while protecting patients and maintaining regulatory trust. This opportunity matters because patient safety is central to benefit-risk decision-making, signal evaluation, and inspection readiness across AstraZeneca's oncology, respiratory, cardiovascular, and specialty pipelines. The director will lead a regional group, connect safety enablement with cross-functional partners, and shape safety strategy in a global environment. For experienced pharmacovigilance professionals, this is a compelling chance to combine scientific rigor, people leadership, digital innovation, and external regulatory engagement. It offers high visibility, responsibility for compliance and process improvement, and the ability to accelerate safe access to transformative therapies worldwide.
Senior Medical Writer
Parexel
Bangalore5+ Years · Remote7 OctParexel is hiring a Senior Medical Writer for its India-Bengaluru-Remote team. The role focuses on clinical trial disclosure and transparency, with responsibilities spanning regulatory document writing, disclosure submissions, client guidance, project management, and mentoring.
Quality Specialist (QMS, Documentation)
Merck
Bangalore5+ Years · Onsite4 OctQuality Assurance Specialist responsible for maintaining the Quality Management System, leading quality activities, ensuring regulatory compliance, and strengthening product and process quality within Merck's Life Science division in India.
Expert - Regulatory Labelling Operations
Merck KGaA
Bangalore5+ Years · Onsite3 OctThe Expert - Regulatory Labelling Operations role focuses on global labeling operational excellence, process optimization, compliance tracking and continuous improvement within Regulatory Quality Safety (RQS).
Assistant Manager, Clinical Data Management
Teva Pharmaceuticals
Bangalore5+ Years · Onsite2 OctLeads and supports Clinical Data Management delivery with subject matter expertise, study oversight, quality control and process improvement. The role combines technical CDM expertise with resource coordination, mentoring, standards development and audit support.
Senior Analyst – Clinical Study Data & CRO Performance Management
Gsk
Bengaluru5+ Years · Hybrid1 OctThis Senior Analyst – SD Performance role sits within GSK's Data Science and Clinical Systems function in Bengaluru, the engine room behind the company's global vaccine and specialty medicine trials. The position owns the strategic, contractual and performance-management layer of GSK's clinical outsourcing model, ensuring preferred CRO partners delivering data management and clinical systems work to benchmark quality, cost and timeline standards. Because GSK's R&D pipeline spans respiratory, immunology and inflammation, oncology, HIV and infectious diseases, reliable CRO performance directly protects trial integrity and submission timelines. For professionals with clinical research or clinical systems experience, this is a rare chance to move from hands-on execution into strategic service-delivery leadership inside a top-tier global biopharma, with visibility across global stakeholders and genuine scope to shape how GSK manages its external data-science ecosystem.
Assistant Clinical Project Manager
Clario
Bangalore0-2 Years · Remote1 OctSupport clinical project managers with study administration, financial tracking, cross-functional coordination, Salesforce configuration and clinical research operations while ensuring quality, compliance and timely delivery.
Medical Writing Specialist
Novo Nordisk
Bangalore5+ Years · Onsite1 OctSenior medical writing specialist role responsible for leading clinical reporting deliverables, setting direction for complex medical writing work, coordinating global stakeholders, and driving quality and process improvements across clinical development programmes.
Manager - Legal
Motherhood Hospitals
Bangalore5+ Years · Onsite1 OctLead all aspects of corporate legal operations, contract drafting, litigation management, and stakeholder advisory.
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.
GPV Professional, Case Processing
Teva Pharmaceuticals
Bangalore0-2 Years · Onsite30 SeptSupport global pharmacovigilance case processing by accurately processing adverse events, maintaining high-quality safety data, performing medical coding and data verification, managing follow-ups, and meeting regulatory and operational timelines.
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.
Patient Care Coordinator
HCG (Healthcare Global Enterprises Ltd.)
Bangalore0-2 Years · Onsite30 SeptDrive patient experience management and feedback analytics across hospital chains to ensure high NPS and operational excellence.
Associate Director, Real World Data Statistics
AstraZeneca
Bengaluru5+ Years · Hybrid29 SeptAlexion, AstraZeneca's rare disease unit, is expanding its epidemiology and real-world evidence capability in Bangalore with an Associate Director I/II, Real World Data Statistics. This individual-contributor leadership role sits at the intersection of advanced biostatistics and regulatory science, converting disease registry, natural history, EMR and claims data into evidence robust enough to withstand FDA, EMA and other health authority scrutiny. The position matters because rare disease programmes depend on external data to characterise small, dispersed patient populations, support label expansions and satisfy post-market commitments. For an experienced statistician it offers unusual scope: methodological innovation in missingness, linkage and confounding control, direct exposure to health authority interactions, and mentorship of a growing RWD statistics function within a biotech-paced, patient-centred environment backed by AstraZeneca's global scale.
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.