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Showing posts with the label Research Analyst Jobs in Pharma Industry

Business Analyst Healthcare Job 2026 at 1Lattice | Pharma Consulting & Analytics Jobs India

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Business Analyst Healthcare Job 2026 at 1Lattice | Pharma Consulting & Analytics Jobs India  (Business Analyst Healthcare Job 2026) Introduction If you are planning to move into high-growth career paths like pharma consulting, healthcare analytics, or market research, this opportunity can be a strong stepping stone. In 2026, roles that combine data analysis with healthcare knowledge are in high demand, especially in consulting and strategy domains. 1Lattice is hiring for the role of Business Analyst – Healthcare & Lifesciences. This position is ideal for candidates from Pharmacy, Life Sciences, or related backgrounds who want to work in analytics-driven decision-making roles. This job not only offers exposure to real-world healthcare problems but also builds strong foundations in consulting, data analytics, and business strategy. About The Company 1Lattice is a fast-growing consulting and analytics firm that provides research-driven insights and decision-support so...

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"Makrocare Careers 2025 | Regulatory Affairs, CQA, Research & Proposal Analyst Jobs in Hyderabad"

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"Makrocare Hiring in Hyderabad 2025 | Regulatory Affairs, CQA, Research, and Proposal Analyst Jobs" (Makrocare Careers 2025) Makrocare, a leading global Clinical Research Organization (CRO) and regulatory solutions provider, is expanding its workforce in Hyderabad, India . The company is inviting applications from talented professionals in Regulatory Affairs, Clinical Quality Assurance (CQA), Research Analysis, and Proposal Management . If you are a Life Sciences, Pharmacy, or Biotechnology graduate looking for growth in regulatory publishing, submissions, compliance, or clinical research , this is an excellent career opportunity. Available Positions at Makrocare:- 1. Associate – Regulatory Affairs (Publishing): Experience: 1–3 years Location: Hyderabad Responsibilities: Prepare and compile eCTD/aCTD submissions for US/UK/EU/ROW. Conduct quality checks and ensure compliance with global regulatory standards. Collaborate with internal teams and respond to quer...

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