
Devendra Kumar Rajora
With a robust 15-year background in Clinical Research, I bring extensive experience as an accomplished Clinical Project Management... | Delhi, Delhi, India
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Devendra Kumar Rajora’s Location Delhi, Delhi, India
Devendra Kumar Rajora’s Expertise With a robust 15-year background in Clinical Research, I bring extensive experience as an accomplished Clinical Project Management professional. I possess a comprehensive understanding of the entire clinical development lifecycle, including initiation, planning, execution, monitoring, and close-out phases, with hands-on experience in managing both Global and Regional clinical studies, including medical device studies. I excel in leading clinical studies across all phases, from Phase 1 to Phase 4 for drug development, as well as Pre & post marketing studies for medical devices, encompassing registries, RWE, and PMCF studies. My expertise ensures precision in execution and impeccable data delivery while adhering strictly to regulatory standards such as ICH-GCP, FDA, EU CTD/CTR, MHRA, ISO 141455, SOP, Protocol, and other pertinent guidelines. I have successfully overseen Global Clinical Studies spanning APAC, EMEA & US regions, demonstrating adept management and leadership skills. As the primary operational contact for clinical studies, I have demonstrated expertise in overseeing critical aspects such as site evaluation, initiation, and close-out visits, managing study timelines, facilitating effective communication, and contributing to SOP development. Additionally, my skill set covers Project Management, Clinical Operations, Line Management, Vendor Coordination, AOP Planning, effective leadership, and seamless collaboration with Business Units. My skills also include collaborating with CROs and vendors, providing valuable input into study protocols and reports, and adeptly identifying and addressing operational challenges. I am strongly committed to ensuring regulatory compliance and supporting colleague training initiatives. 5 years of Line Management experience for assigning, directing work, appraising performance & guiding for professional development of team. Extensive experience of end-to-end process of creation, set-up & maintenance activities of TMF & Document Management. Acting as SME & technology expert for eTMF inspection readiness for study team by delivering various KPI reports to achieve compliance. Areas of Expertise: • Project Management • Clinical Operations • Delivery Management • Line Management • Process Improvement • Financial Analysis & Budget Forecasting • Team Development • Driving New Initiatives
Devendra Kumar Rajora’s Current Industry Novartis
Devendra
Kumar Rajora’s Prior Industry
Gvk Bio
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Siro Clinpharm
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Clinirx Research
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Quintiles
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Medtronic
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Novartis
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Work Experience

Novartis
Strategy & Operations Manager
Fri Sep 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed May 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time)
Medtronic
Clinical Research
Mon Oct 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Aug 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Quintiles
Sr.Centralized Monitoring Lead
Mon Dec 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Oct 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Clinirx Research
Senior CRA
Sat Sep 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Nov 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Siro Clinpharm
CRA
Mon Aug 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Oct 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Gvk Bio
CRA
Wed Oct 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jul 01 2011 00:00:00 GMT+0000 (Coordinated Universal Time)