Clinical Trials Jobs in Rājkot
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Search Results - Clinical Trials Jobs in Rājkot
vueverse.-Rājkot
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.-Rājkot
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...
TWO95 International, Inc-Rājkot
R)
• Hands-on experience with statistical analysis 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...
Advanced Clinical-Rājkot
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...
Cytel-Rājkot
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 Observer-Rājkot
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...
Simelabs - Digital, AI/ML, Automation, Robotics, Gen AI.-Rājkot
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...
Michael Page-Rājkot
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...
appcast.io -
Cytel-Rājkot
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...
Trigent Software - Professional Services-Rājkot
We are currently seeking a Statistical Programmer to join our diverse and dynamic team. As a Statistical Programmer, you will play a vital role in the development, validation, and execution of statistical programs to support clinical trial analysis...
Nityo Infotech-Rājkot
development, clinical trials, and commercialisation. Your contributions will play a key role in accelerating our mission to bring life-saving treatments to market more efficiently.
The AI Software Engineer will undertake the design, implementation...
Cytel-Rājkot
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 Oncology-India
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...
Tech Observer-Mumbai, 419 km from Rājkot
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...
Cytel-Delhi, 958 km from Rājkot
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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