HYDERABAD · FULLTIME
Analyst

Globaldata
Hyderabad · onsite · Posted 2d ago
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₹7.0L - ₹11.0L PA4–9 yrsfulltimeHyderabad
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Section · 01
About this role
Roles and Responsibilities :
- Conduct literature reviews to identify relevant patents, protocols, and clinical trial data related to pharmaceutical products.
- Analyze complex scientific information from various sources such as PubMed, Google Scholar, and industry publications.
- Develop comprehensive reports summarizing findings and providing recommendations for product development based on patent analysis.
- Collaborate with cross-functional teams including researchers, engineers, and regulatory affairs specialists to ensure compliance with T&C requirements.
Job Requirements :
- Master's degree in Pharmacy (M.Pharm), M. Tech., PHd Inc., or equivalent qualification.
- 4-9 years of experience in a similar role within the pharmaceutical industry.
- Strong understanding of clinical trials, patents, protocols, and regulatory guidelines governing pharmaceutical products.
- Excellent analytical skills with ability to interpret complex scientific data.
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Section · 02
Skills
Gene EditingNucleic AcidPostdocAsoPhDclinical trialsprotocolsPatentstMpharmLiterature ReviewCARmtechcell therapypubmedAntibody Engineering
Section · Company
About GlobalData

Globaldata
Analytics & KPO
2.0k+
employees
1984
42 years old
Hyderabad / Secunderabad, Telangana
India
₹7L – ₹11L PA
This role
About
GlobalData provides unique data, expert analysis & innovative solutions to companies in the world's largest industries
Industries
Analytics & KPOConsulting
Employee ratings
1,042 reviews
3.3/ 5
Culture
3.4
Career growth
2.6
Work-life
3.5
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