Clinical Trials Jobs in Jūnāgadh
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Search Results - Clinical Trials Jobs in Jūnāgadh
vueverse.Jūnāgadh
business and account expansion across Biostatistics, Statistical Programming, and Data & Analytics services supporting global clinical trials and regulatory submissions.
Core Responsibilities
• Drive new business acquisition for Clinical Biometrics...
Micro Crispr Pvt. Ltd.Jūnāgadh
Medical Oversight
• Provide ongoing medical monitoring of assigned clinical trials, including real-time safety review of adverse events (AEs) and serious adverse events (SAEs).
• Evaluate safety signals, trends, and laboratory/ECG abnormalities...
SIROJūnāgadh
Create eCRF specifications, design, develop and validate clinical trial setup process
• Create edit check specifications and setup edit checks at trial level
• Implement UAT scripts to test the setup of the clinical study
• Setup different...
Micro Crispr Pvt. Ltd.Jūnāgadh
Medical OversightProvide ongoing medical monitoring of assigned clinical trials, including real-time safety review of adverse events (AEs) and serious adverse events (SAEs).Evaluate safety signals, trends, and laboratory/ECG abnormalities to ensure...
Advanced ClinicalJūnāgadh
The Principal Statistical Programmer (“Programmer”) will have experience in all required areas of a Senior Statistical Programmer. The Principal Statistical Programmer is responsible for providing statistical programming services for assigned clinical trials...
CytelJūnāgadh
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...
Tech ObserverJūnāgadh
documentation (e.g. data validation guidelines).
Review and interpret Report and Analysis Plans and provide comments for assigned projects.
Develop and review SAS programs and output for the management of clinical trial data, the tabulation of data...
IQVIA IndiaJūnāgadh
Role : Principal Statistical Programmer
Skill : SDTM, Adam, TLF, Clinical Trials
Mode : Hybrid/Remote
Experience : 9-14 years
Educational Qualification: Bachelor's Degree Statistics, Computer Science or related field Req
Job Overview...
Michael PageJūnāgadhappcast.io
documentation, and respond to regulatory queries for clinical trials or product approval.
Technology Transfer & Collaboration
• Coordinate tech transfer from lab to pilot and commercial scale in collaboration with Manufacturing, QA/QC, and Engineering teams...
CytelJūnāgadh
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...
DAVA OncologyIndia
to: clinical trial research and communications, drug or trial publication research and review, and oncology conference meeting reviews. Candidates with previous experience in the oncology therapeutic area are highly desirable.
Responsibilities:
• Conduct...
Simelabs - Digital, AI/ML, Automation, Robotics, Gen AI.Jūnāgadh
Key Responsibilities
• Develop, validate, and maintain ADaM datasets, TLFs, and other analytical outputs for clinical trials.
• Support Oncology studies by ensuring accuracy, consistency, and regulatory compliance in all programming deliverables...
Tech ObserverMumbai, 371 km from Jūnāgadh
and Local Regulatory Guidelines for study specific deliverables (including but not limited to; Clinical Trial Management System, Study Equipment's, Travel Arrangements, Couriers, etc.) in delegated projects.
• Develop study management plans and generate...
SourcebaeJūnāgadh
effort; sleep/disordered breathing)
Nonlinear, Statistical, and Adaptive Signal Analysis
Multichannel, Spatial, and Connectivity Signal Analysis
Machine Learning and Data‑Driven Biomedical Signal Analysis
Clinical Monitoring, Wearable, and Translational...
CytelDelhi, 1045 km from Jūnāgadh
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 valuesWe...
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