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  • Active Jobs Found
    (Last Updated: Jul 23, 2026)
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Staff Nurse

Vikram Hospital

Full time
  • 1+ years
  • Not Disclosed
  • Bengaluru, Karnataka, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 1+ years
  • Not Disclosed
  • Bengaluru, Karnataka, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesExplains the four stages in the Nursing Process and demonstrates an understanding of the beginning nurse role in the health service. Plans and performs Nursing Care by using the Nursing process.Observes patient’s condition and take suitable action accordingly and/or report changes to the Head Nurse and/or to the physician.Converts and calculates dosages. Assisting Doctors for various surgical and medical diagnostic procedures by using aseptic technique. Knows the correct method of collecting and sending specimens to laboratory for diagnostic tests. Assisting with diagnostic tests/ biopsies, lumbar punctures, etc.Demonstrates correct technique of checking and recording Vital signs.Assisting with therapeutic procedures such as Venipunctures, I.V. therapies, transfusion etc.Carry out the procedures of Admission, Transfer, Discharge and Death of patient as per hospital policy. Attends/ Takes rounds with the Doctors and carries the orders accordingly.Can define asepsis and aseptic technique and uses sterile technique when require.Correctly calculates the infusion rate for Infusions and demonstrates the ability to solve intravenous infusion problems. Calculate ml per hr, drops per minute and correctly uses intravenous safety devices.

  • Nurse

Bio Chemist

G. Kuppuswamy Naidu Memorial Hospital

Full time
  • 2+ years
  • Not Disclosed
  • Greater Noida Uttar Pradesh, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 2+ years
  • Not Disclosed
  • Greater Noida Uttar Pradesh, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

Qualification & Experience                        Experience 2 to 5 years ExperienceQualifications M.Sc. Bio ChemistryKey Skillshigh analytical accuracy, proficiency in operating automated lab equipment, deep knowledge of clinical pathology, and strong communication skills          

  • Others
  • Communication

Zonal Manager

Alembic Pharmaceuticals

Full time
  • 2+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 2+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesEnsure and assist to manage achievement of month on month sales targets and market beating growth on product-wise / value-wise primary and secondary sales, territory profitability, increase / maintain brand market shares through effective planning of resources, distribution management, customer relation management / key opinion leader engagement initiatives and control on expenses. Implementation of company’s’ promotional strategies and inputs and ensure desired outcomes are achieved. Prepare the budget and align the resource plan to meet the business objectives of the Company (territory) and ensure optimal deployment to ensure profitability of the assigned territory. Develop and execute market intelligence plan to obtain feedback on market conditions and impact of promotional strategy on movement of company’s products as well as that of competitors. Develop relationship with key customer and ensure effective follow up for desired outcomes.

  • clinical research
  • Operations
  • hospital management

Senior Manager

Alembic Pharmaceuticals

Full time
  • 3+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 3+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesQuarterly Investor Communication: Lead the preparation of quarterly investor presentations and press releases. Ensure financials, disclosures, and messaging are accurate, consistent, and fully compliant with regulatory requirements Pre-Quarter Analysis & Consensus Tracking: Support the preparation of pre-quarter Investor/ Analyst FAQs and maintain pre and post-results consensus tracking Competitive Intelligence & Insights: Develop comprehensive competitor deep-dive dashboards and presentations. Deliver both quantitative analysis and qualitative insights to support management decision-making Investor Engagement Support: Support execution of roadshows, conferences, and investor meetings through preparation of presentations and FAQs. Maintain consistent engagement with key stakeholders across the investor ecosystem Investor & Analyst Interface: Ensure timely, accurate, and well-articulated responses aligned with company messaging for analyst/ investor queries Shareholding Analysis & Engagement Strategy: Monitor weekly shareholding patterns and identify key trends. Use insights to structure targeted investor engagement strategies aimed at optimizing shareholder mix and value Investor Feedback & Market Perception Tracking: Capture and synthesize feedback from investors and analysts post interactions. Highlight perception gaps, key concerns, and valuation drivers, and feed insights into internal strategy and communication planning Investor Benchmarking: Conduct periodic benchmarking against peers on shareholding profile, analyst coverage, and valuation positioning. Identify gaps and recommend actions to strengthen investor positioning Data management & Tracking: Maintain investor database, analyst coverage tracker, and IR calendar. Ensure timely updates to IR website and disclosures. Build robust internal trackers for investor interactions and follow-ups

  • Operations
  • hospital management
  • Inspection

Medical Representative

Alembic Pharmaceuticals

Full time
  • 3+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 3+ years
  • Not Disclosed
  • Mumbai, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesCarrying out effective field work to achieve and surpass the assigned budget by generation of prescriptions through medical professionals (HCPs). Carrying out the effective RCPA and entering the correct information in the system and prepare / set objective (Pre Call Planning) for every Doctor call. Demonstrate and promote products to HCPs (doctors and pharmacists) as per the guidelines provided by the division to generate maximum prescriptions. Ensure regular customer conversion, no prescriber loss by following the division strategy by building effective relationship. Ensure the sufficient availability of the products at the pharmacists to honor the Doctor prescription and do the required number of POBs as per the division norms. Create / update the effective Doctor / Chemist list as per the division guidelines. Ensure the success of new launches by implementing the strategies suggested by the division. Managing distribution channel members such as Stocki

  • Operations
  • hospital management
  • Inspection

Chemicals Research Senior Analyst

Accenture

Full time
  • 2+ years
  • Not Disclosed
  • Gurugram, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 2+ years
  • Not Disclosed
  • Gurugram, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesAssisting and supporting the development of thought-provoking insights through market analysis and in-depth review of trends. Drawing on both traditional and innovative data sources and research methodologies to explore key questions. Analyzing large datasets and interpreting results using statistical techniques and data visualization tools Updating our proprietary in-house models and provides results to the practice when needed. Developing research insights and compelling business narratives alongside research leads. Presenting key findings in a structured and concise manner (with focus on insights).

  • clinical research
  • Operations
  • Clinical Trial
  • Inspection

Chemicals Research Specialist

Accenture

Full time
  • 5+ years
  • Not Disclosed
  • Gurugram, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 5+ years
  • Not Disclosed
  • Gurugram, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

Responsibilities Assisting and supporting the development of thought-provoking insights through market analysis and in-depth review of trends. Drawing on both traditional and innovative data sources and research methodologies to explore key questions. Analyzing large datasets and interpreting results using statistical techniques and data visualization tools Updating our proprietary in-house models and provides results to the practice when needed. Developing research insights and compelling business narratives alongside research leads. Presenting key findings in a structured and concise manner (with focus on insights). “Hard” skills: Ability to use techniques such as secondary research, company and market analysis, strategic analysis frameworks, interview-based research and financial analysis. Strong analytical skills and a proven ability to make sense out of data, with ability to analyze, visualize, and interpret Able to learn and embrace new sources, tools, and skills, including alternative modes of research delivery/data visualization tools (e.g., Power BI, Qlik etc.). Compiling reports/analysis with clear storyline and results. A basic understanding of the role of digital / technology in disrupting chemical markets Able to write in a clear, concise, and compelling way Strong PowerPoint, Excel, and Word skills “Soft” skills: Strong interest in the Chemical industry and Technology Intellectual curiosity and desire to learn more and grow Problem solver approach to work Proven ability to work independently, collaboratively, and virtually - in a global, multi-cultural, multi-time zone team Ability to present research findings to team and Accenture executives Strong communications skills and good interpersonal skills Strong professional qualities: client focus, decisiveness, integrity, resilience to stress against stretch goals and deadlines Ability to work on multiple engagement. Qualification & Experience A bachelor’s degree, preferably in a science or engineering. A PG degree in business, such as business (MBA), economics or equivalent is a plus. Work Experience: 5-7 years of business experience, preferably in a consulting environment, think tank, financial institution, or other 3rd party business research organization or demonstrated equivalent skill."

  • clinical research
  • Operations
  • Clinical Trial
  • Inspection
  • 8+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 8+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesAnalyze industry and company data using research and visualization tools. Work with senior researchers to update internal models and produce client-ready outputs. Work with research leads and client teams to shape viewpoints, answer strategic questions, and contribute to publications or internal briefings. Craft clear and compelling research outputs (slides, visualizations, written summaries) for Accenture leadership and clients. Develop case studies, conduct surveys, and perform secondary data analysis. Comfortable with expert interviews. Leverage generative AI to enhance ways of working, identify novel insights, and deliver outputs in non-traditional ways “Hard” skills: Understanding of the Life Sciences (pharmaceutical) industry and its key challenges Experience applying a range of research methodologies, including secondary research, market and company profiling, strategic frameworks, and financial analysis. Strong analytical skills with the ability to make sense out of data, visualize, and interpret findings Comfortable using Generative AI tools (e.g., ChatGPT, Claude, Copilot) to enhance research and content creation. Business knowledge on the application of AI (including machine learning, deep learning, natural language processing, large language models (LLMs), generative AI, agentic AI, etc.) and related emerging topics in AI, Data, Automation, Analytics. Qualification & ExperienceA bachelor’s degree, preferably in business or STEM. A postgraduate degree in business or STEM, such as an MBA, MS, PhD., or equivalent is a plus. Work Experience: 8-10 years of experience, preferably in a consulting environment, think tank, financial institution, pharmaceutical/biotech company, CRO/CDMO or other business research organization or have demonstrated equivalent skill elsewhere

  • clinical research
  • Operations
  • Clinical Trial
  • Inspection

Manager, Regulatory Clinical Trials

Takeda Pharmaceutical

Full time
  • 5+ years
  • Not Disclosed
  • Gurgaon, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 5+ years
  • Not Disclosed
  • Gurgaon, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesManage and lead preparation, submission, and tracking of CTAs, substantial/non-substantial amendments, notifications, and other required submissions to Indian Health Authorities (CDSCO) as applicable. Ensure timely, complete, and compliant responses to HA questions/deficiency letters to prevent avoidable approval delays. Drive readiness and coordination for HA meetings/interactions, including SEC briefing preparation, Q&A preparation, and stakeholder alignment. Provide regulatory guidance to study teams on India clinical trial requirements, expectations, and risks; translate requirements into actionable submission plans. Oversee regulatory compliance monitoring during study conduct, including compliance with regulatory commitments and conditions of approval. Closely cordinate with the Global/International Regulatory Clinical Trials team, GDO, India R&D, Medial team and external partners (e.g., CROs) for regulatory afairs stregies on Clinical trials in India. Provide regulatory consultation and guidance to cross-functional study teams on Indian clinical trial requirements, expectations, and risks; translate requirements into actionable submission and mitigation plans. Monitor, analyze, and communicate regulatory intelligence related to Indian regulations, guidance, and evolving HA/SEC expectations; assess impacts on the pipeline and studies, and recommend actions. Support policy advocacy activities by providing technical and regulatory input, supporting position development, and engagement planning (as appropriate) with industry forums/associations and external stakeholders to help shape a favorable clinical trial regulatory environment.Qualification & ExpeirneceBachelor’s degree in Pharmacy, Life Sciences, Medicine, or related field (advanced degree preferred). Minimum 5 years of experience in pharmaceutical industry or CRO for managing regulatory affairs for Clinical trial in India. Demonstrated experience in clinical trial regulatory affairs in India, including CTA submissions and amendments.

  • Operations
  • hospital management
  • Medical Writing

GCM Medical Operations & Governance Lead

Takeda Pharmaceutical

Full time
  • 3+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026
  • 3+ years
  • Not Disclosed
  • Bengaluru, India
  • Post Date: Jun 11, 2026
  • End Date: Aug 11, 2026

ResponsibilitiesLead the centralized Medical Operations & Governance team within the Bengaluru Global Capability Center GCC), delivering SOP & documentation governance, CAPA coordination, vendor management, grant reconciliation, and purchase order management for Medical Affairs Manage a mid-sized team providing operational governance and compliance services across Global Medical Establish and serve as site lead for the Bengaluru Medical GCC, building organizational capabilities, defining operating rhythms, and fostering a high-performance, compliant, and collaborative culture aligned with Global Medical prioritiesSOP & Documentation Governance: Lead end-to-end SOP and documentation governance across Medical activity domains, ensuring lifecycle processes are consistently applied, high-quality standards are maintained, and documentation remains inspection-ready across the Medical Governance Office portfolio and local GCM activities. Establish and continuously evolve Records Information Management (RIM), central documentation storage and archiving, templates, and governance controls — driving standardization, monitoring adherence, and ensuring effective management of deviations and controlled exceptions across Medical execution CAPA Coordination: Own oversight of CAPA processes across the Medical Governance Office, ensuring timely identification, tracking, and resolution of issues; implement governance mechanisms to monitor performance, enforce accountability, and maintain audit readiness Proactively assess CAPA trends and systemic risks, driving escalation where needed and partnering with stakeholders to strengthen root cause resolution and prevent recurrence Vendor Operations & Grant Management: Lead workflow design and lifecycle management of vendor operations and grant management processes in partnership with Procurement, Medical Business Operations, and Medical Governance Office, ensuring performance oversight, contractual compliance, and standardized execution across supplier base Oversee workflows in medical grant and sponsorship validation and reconciliation processes, ensuring alignment between approved terms, deliverables, and financial records; drive consistency and control in accordance with Takeda financial and compliance requirements Contract Operations and Procurement Support: Oversee GCM-based contract operations team, ensuring efficient PO workflows within Business Operations processes, payment integrity, and adherence to financial and operational governance standards Drive coordination with Business Operations, Finance, and Procurement to ensure accurate spend tracking, timely reconciliation, and continuous improvement of process efficiency and transparency Ensure robust vendor onboarding and documentation governance processes are in place, maintaining complete, compliant, and audit-ready operational records

  • Operations
  • hospital management
  • Medical Writing

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