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Clinical Trials Jobs in Nadiād

1 - 7 of 7
1 - 7 of 7
Search Results - Clinical Trials Jobs in Nadiād
apartmentTech ObserverplaceNadiādevent_available
Responsible for coordinating and performing (if applicable) the collection, distribution and storage/ archival of data/ study material/ study supply generated (for assigned studies) during clinical research trials. Responsible to ensure...
apartmentVeeda LifesciencesplaceNadiādevent_available
Preferred Skills:  •  Experience in QMS and ISMS in Clinical Research Organizations and/or pharmaceutical companies with previous experience in system audits and/or inspections by certification bodies  •  Experience in Phase 1 to 4 Clinical Trials...
apartmentClinoGenesis Research InstituteplaceNadiādevent_available
in coordinating clinical trial activities, including organizing study documents, communicating with research teams, and maintaining accurate trial records. Daily responsibilities include supporting informed consent processes under supervision, helping ensure...
apartmentMS CLINICAL RESEARCHplaceNadiādevent_available
Job Description: Data Monitoring & eCRF Design Specialist Role Overview The Data Monitoring & eCRF Design Specialist will be responsible for designing, managing, and monitoring clinical trial data systems to ensure accuracy, completeness...
apartmentClinoGenesis Research InstituteplaceNadiādevent_available
documents. GCP Compliance: Ensure all trial activities follow Good Clinical Practice guidelines. Audit Support: Assist the team during monitoring visits and site audits. Education Qualification: B.Sc / M.Sc in Life Sciences (Microbiology, Biotechnology...
apartmentMS CLINICAL RESEARCHplaceAnand, 18 km from Nadiādevent_available
Job Description: Data Monitoring & eCRF Design Specialist Role Overview The Data Monitoring & eCRF Design Specialist will be responsible for designing, managing, and monitoring clinical trial data systems to ensure accuracy, completeness...
apartmentTech ObserverplaceAnand, 18 km from Nadiādevent_available
Responsible for coordinating and performing (if applicable) the collection, distribution and storage/ archival of data/ study material/ study supply generated (for assigned studies) during clinical research trials. Responsible to ensure...

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