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...
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Veeda Lifesciences-Sūrat-
Experience Required:
• Experience in Phase 1 to 4 Clinical Trials Europe and India
• Industry experience of 15 to 20 years
Preferred Skills:
• Experience in QMS and ISMS in Clinical Research Organizations and/or pharmaceutical companies...
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Concept Medical-Sūrat-jmmst.com-
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...
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ProductLife Group-Sūrat-
Education & Experience
• Doctor or pharmacist by training
• Minimum 4 years experience working for service providers performing QC of case
• Minimum 3 years of experience in processing Clinical Trial cases.
• SafetyEasy/ Argus database experience
Profile...
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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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Safeguard Global Recruiting-Sūrat-
of project management principles, methodologies, and processes
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
• At least 2 years’ experience working in clinical trials.
• Demonstrable experience in the management or coordination of clinical trials...
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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...
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Safeguard Global Recruiting-Sūrat-
and implementation of project management methodologies and processes.
Responsibilities
3. 5 years industry experience including at least 1 year in Project Management roles in clinical trials within a CRO, pharmaceutical or biotech setting.
Good knowledge of the drug...
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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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Advanced Clinical-Sūrat-
programming experience or related analytic tool in pharmaceutical development or CRO environment preferred, but not required
• Good knowledge of medical terminology and conduct and analysis of clinical trials
• Knowledge of relevant industry data standards...
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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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United HR Solutions-Sūrat-mncjobsindia.com-
Ensure clinical investigations comply with ISO 14155 2020 and ICH-GCP guidelines Oversee regulatory submissions and study approvals in alignment with the New Drugs and Clinical Trials Rules NDCTR 2019 Coordinate biocompatibility evaluations...
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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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Advanced Clinical-Sūrat-
services for assigned clinical trials. This includes acting as the lead programmer for assigned clinical trials. Responsibilities Exceed expectations and responsibilities of a Senior Statistical Programmer Understand and implement CDISC and other regulatory...
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Safeguard Global Recruiting-Sūrat-
Management roles in clinical trials within a CRO, pharmaceutical or biotech setting'
• Good knowledge of the drug development process, associated regulatory and ICH GCP guidelines and their application to clinical trials.
• Detailed and proactive approach...
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