Job Description
1.Maintaining the source documents, CRFs, Investigator Site File and other study relateddocuments according to ICH-GCP guidelines
2.Completing the eCRF
3.Maintenance of Investigational Product according to the specific temperature.
4.Preparing for site qualification visits, initiation visits, monitoring visits and site close out visits.
5.Organizing ethics committee meetings
6.Completing the review forms and submitting all study related documents to EC
7.Coordinating with the local labs, central labs
8.Assistance in Safety Reporting within the required timelines.
9.Assistance in patient selection and recruitment
10.Assistance in Informed Consent Process
Interested candidates are requested to send across their resumes to the mail id info@clinovex.com or you can also contact us at this number: 8891000510
2.Completing the eCRF
3.Maintenance of Investigational Product according to the specific temperature.
4.Preparing for site qualification visits, initiation visits, monitoring visits and site close out visits.
5.Organizing ethics committee meetings
6.Completing the review forms and submitting all study related documents to EC
7.Coordinating with the local labs, central labs
8.Assistance in Safety Reporting within the required timelines.
9.Assistance in patient selection and recruitment
10.Assistance in Informed Consent Process
Interested candidates are requested to send across their resumes to the mail id info@clinovex.com or you can also contact us at this number: 8891000510
Salary: INR 50,000 - 1,00,000 P.A
Education:
UG - B.Tech/B.E. - Bio-Chemistry/Bio-Technology, Diploma - Other Specialization
Candidates who have completed PG Diploma Course in Clinical Research are preferred.
Candidates who have completed PG Diploma Course in Clinical Research are preferred.
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