Clinical Trials Jobs in Rājahmundry
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Search Results - Clinical Trials Jobs in Rājahmundry
Planet PharmaRājahmundry
SUMMARY
We are seeking a Senior Clinical Trials Feasibility Data Scientist with strong expertise in clinical analytics, machine learning, and AI-driven workflows.
In this role, you will design and deliver intelligent analytics solutions...
Hvantage Technologies Inc USARājahmundry
Clinical Payments Specialist with a minimum of 3+ years of experience in international accounting and clinical trial financial systems. A critical requirement for this role is advanced proficiency in Medidata CTMS, specifically regarding budget...
Trigent Software - Professional ServicesRājahmundry
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...
CytelRājahmundry
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...
EphicacyRājahmundry
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...
TalentHawkRājahmundry
experience in global data protection frameworks within the life sciences sector, particularly relating to clinical trial data, patient safety data, and pharmacovigilance systems.
Key Responsibilities
• Provide Data Protection Officer (DPO) expertise across...
EphicacyRājahmundry
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...
IQVIARājahmundry
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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