Clinical Trials Jobs in Nellore
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Search Results - Clinical Trials Jobs in Nellore
Trigent Software - Professional ServicesNellore
validating, and maintaining statistical programs to support clinical trials and data analysis.
Key Responsibilities
Develop and maintain statistical programming deliverables using R and/or SAS.
Perform data manipulation, analysis, and reporting using R...
vueverse.Nellore
and presentation skills
Preferred Skills
• Experience interacting with KOLs / HCPs (scientific exchange)
• Exposure to clinical trials / publications / medical content
• Understanding of compliance and regulatory frameworks...
CytelNellore
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
Our values
We...
IQVIA IndiaNellore
and oversight of centralized monitoring activities to ensure subject safety, data integrity, regulatory compliance, and delivery of clinical trial objectives as per sponsor and contract requirements. The role partners with clinical, project, analytics, quality...
CytelNellore
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...
Insight GlobalNellore
and PowerPoint
What We're Looking For
• 3–5 years of experience working with data in pharma, biotech, or clinical research
• Hands-on experience with CTMS platforms
• Familiarity with external clinical datasets and clinical trial inclusion/exclusion criteria...
EphicacyNellore
EU, WHO, and ANVISA thereby keeping abreast with the current regulations.
• Good understanding of Clinical trial domain.
• Proactive with communication and adaptable in approach while working independently
• Ability to mentor/guide junior programmers...
SIRONellore
Protocol, SAP, Mock Shells, LOT, Analysis plan etc. Hands on experience of development and review of study specific tables, listings and figures for various phases of clinical trials and across TA’s.
SAS Programming
Expertise in Base and Advance SAS...
EphicacyNellore
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-solving skills
• Excellent communication...
IQVIANellore
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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