Clinical Trials Jobs in Vadodara
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Search Results - Clinical Trials Jobs in Vadodara
Concept MedicalVadodara
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...
Veeda LifesciencesVadodara
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...
ProductLife GroupVadodara
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...
Veeda LifesciencesVadodara
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 with previous...
CHETAN MEDITECH PRIVATE LIMITEDVadodara
to provide recommendations on clinical trial strategy. The ideal candidate will bring in-depth knowledge of international medical device clinical research expertise, robust scientific writing capabilities, and demonstrated experience in end-to-end clinical...
Advanced ClinicalVadodara
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...
Safeguard Global RecruitingVadodara
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...
Advanced ClinicalVadodara
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...
CytelVadodara
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...
Safeguard Global RecruitingVadodara
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...
United HR SolutionsVadodaramncjobsindia.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...
Advanced ClinicalVadodara
programming services for assigned clinical trials. This includes acting as the lead programmer for assigned clinical trials.
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Responsibilities
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• Exceed expectations and responsibilities of a Senior Statistical Programmer
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• Understand...
Safeguard Global RecruitingVadodara
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...
Advanced ClinicalVadodara
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...
Teamware SolutionsVadodara
/ statistical programming experience within pharmaceutical clinical development - Supporting regulatory filings (e.g. NDA, BLA, MAA)
• Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory...
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