Clinical Trials Jobs in Sūrat
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Search Results - Clinical Trials Jobs in Sūrat
Signant Health-Sūrat
About Signant Health
At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational...
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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...
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Veeda Lifesciences-Sūrat
regulatory requirements.Essential documents review for clinical trials (including phase trials and patient based multisite BA/BE studies) in compliance with ICH-GCP, Indian GCP, internal procedures, protocol and applicable regulatory requirements,QA review...
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SIRO-Sūrat
Key Accountabilities:
• Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process
• Create edit check specifications and program or modify checks at study level within EDC
• Setup different...
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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...
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Veeda Lifesciences-Sūrat
regulatory requirements.
• Essential documents review for clinical trials (including phase trials and patient based multisite BA/BE studies) in compliance with ICH-GCP, Indian GCP, internal procedures, protocol and applicable regulatory requirements,
• QA...
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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...
Read more
Veeda Lifesciences-Sūrat
regulatory requirements.
• Essential documents review for clinical trials (including phase trials and patient based multisite BA/BE studies) in compliance with ICH-GCP, Indian GCP, internal procedures, protocol and applicable regulatory requirements,
• QA...
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princeps technologies-Sūrat
Job Title: Senior Statistical Programmer (Oncology)
Location: Canada/IN
Employment Type: Full-Time
Experience: 8+
Overview
We are seeking an experienced Senior Statistical Programmer with strong Oncology clinical trial experience to support end...
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Advanced Clinical-Sūrat
and experience.
Training: N/A
Certification: N/A
Experience:
• Minimum 4 years professional experience working with clinical trial documentation and a minimum 2 years of experience in a leadership/people management capacity, or equivalent.
• Advanced...
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Valos Srl-Sūrat
Responsibilities
• Create ADAM and TFLs for clinical studies
• Apply advanced statistical methodologies to clinical trials and RWE studies
• Contribute to the development of Statistical Analysis Plans (SAPs) and study reports
• Collaborate closely with cross...
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Biotech Healthcare-Sūrat
marketing collaterals for both traditional and digital promotional campaigns.
• Provide ongoing support to distributors participating in Product Management Systems (PMS), aiding in Key Opinion Leader (KOL) development.
• Coordinate with the clinical trial...
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Biotech Healthcare-Sūrat
marketing collaterals for both traditional and digital promotional campaigns.
• Provide ongoing support to distributors participating in Product Management Systems (PMS), aiding in Key Opinion Leader (KOL) development.
• Coordinate with the clinical trial...
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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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Ephicacy-Delhi, 940 km from Sūrat
thereby keeping abreast with the current regulations.Good understanding of Clinical trial domain.Proactive with communication and adaptable in approach while working independentlyAbility to mentor/guide junior programmers and successfully taking care...
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