Clinical Trials Jobs in Sūrat
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Search Results - Clinical Trials Jobs in Sūrat
Concept Medical-Sūrat
Clinical Trial Associate
The Clinical Trial Associate provides administrative support to the clinical research teams in the full spectrum of the research activities such as pre-clinical research, study start-up, study management and site closure...
Advanced Clinical-Sūrat
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...
Concept Medical-Sūrat
Clinical Trial AssociateThe Clinical Trial Associate provides administrative support to the clinical research teams in the full spectrum of the research activities such as pre-clinical research, study start-up, study management and site closure...
Cytel-Sūrat
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...
Micro Crispr Pvt. Ltd.-Sūrat
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...
Trigent Software - Professional Services-Sūrat
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...
Advanced Clinical-Sūrat
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...
CloudLabs Inc-Sūrat
industry leading training.
Opportunity to work remotely is available.
Experience Required: Medidata Rave, Custom Function Expert, Clinical Data Management.
Minimum 2-3 years of relevant experience as Medidata Rave EDC programmer and strong experienced...
Tech Observer-Sūrat
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...
Cytel-Sūrat
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...
Michael Page-Sūrat
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 -
Simelabs - Digital, AI/ML, Automation, Robotics, Gen AI.-Sūrat
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 Observer-Mumbai, 236 km from Sūrat
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...
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...
Cytel-Delhi, 940 km from Sūrat
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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