Clinical Trials Jobs in Vijāpura
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Search Results - Clinical Trials Jobs in Vijāpura
Triomics-Vijāpura
About Triomics:
Triomics helps oncology organizations scale clinical research and high-quality data creation without scaling headcount. Our AI platform - powered by OncoLLM™- automates the operational work behind trial screening, eligibility...
Syneos Health-Vijāpura
preferably in a clinical trial environment.
• Excellent written and verbal communication skills.
• Ability to read, write, speak and understand English.
Email your CV on:...
Qinecsa Solutions-Vijāpura
Registration
Experience: 1 - 3 years in Pharmacovigilance
Primary Responsibilities
As a medical reviewer
• Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports
• Determine...
NEXTGEN MEDWORKS-Vijāpura
business across India.
The ideal candidate must have strong exposure to government and private healthcare sectors.
This role requires a combination of sales leadership, clinical support capability, and relationship management within the ENT segment.
Key...
IQVIA-Vijāpura
Hands-on experience in developing and reviewing Data Validation Listings.
• Good understanding of clinical trial data and programming standards.
• Working knowledge of SAS Macros and SQL.
• Strong analytical, problem-solving, and communication skills...
Veramed-Vijāpura
review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author and review simple and complex dataset standards
• Perform data checks and data exploration (e.g. using frequencies, histograms)
• Complete and review CDISC Validation tool...
IQVIA India-Vijāpura
Requires minimum of 6-7 years or more
• Experience in clinical research field preferred.
• Experience level may vary based on customer specific requirements.
• Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical...
Veramed-Vijāpura
listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.
Technical:
• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author and review...
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