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Clinical Trials Jobs in Kochi

1 - 8 of 8
1 - 8 of 8
Search Results - Clinical Trials Jobs in Kochi
TWO95 International, Inc-Kochi-
and reporting in clinical trials  •  Proficient in SAS and R for statistical modelling, efficacy analysis, and data interpretation  •  Ability to collaborate closely with programming and clinical teams in an agile setup....
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CloudLabs Inc-Kochi-
strategic initiatives supporting the Global Clinical IT team. In this role, the individual will be a technical developer to support business initiatives within Medidata Rave suites of applications. This individual should have demonstrated prior experience...
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Cytel-Kochi-
that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials. Responsibilities As a Principal Statistical Programmer, your...
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Infodesk-Kochi-
with pharmaceutical content such as clinical trials, compounds, indications, and related subject matter is important to our collective success. Scope of Work: Attention to detail involving relevance, grammar, context and instructions. Adhere to journalistic standards...
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princeps technologies-Kochi-
requires strong technical proficiency, autonomy, and the ability to collaborate effectively within cross-functional and global teams. Core Responsibilities  •  Program, validate, and maintain clinical trial datasets and outputs using SAS and R.  •  Lead...
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Ephicacy-Kochi-
survival)  •  Familiarity with data visualization techniques and tools in R  •  Experience with clinical trial data and familiarity with CDISC ADaM and SDTM standards  •  Knowledge in Industry R packages like ADMIRAL and OAK  •  Strong analytical and problem...
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SUN PHARMA-Kochi-
experience in processing clinical trial data in the biotechnology, pharmaceutical, CRO or health care related industry.  •  Oncology Therapeutic area preferred.  •  Strong SAS programming skills in a clinical data environment with excellent analytical skills...
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IQVIA-Kochi-
review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary  •  Compose, edit and medically review...
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