Sr. Research Associate/ Associate Scientist (Clinical Research Physician)
Ahmedabad, Gujarat
Veeda Clinical Research
Job Description
1 Protocol, Informed Consent From (ICF), case report form (CRF) Preparation:
• Coordinate with clinical research personal for of Protocol.
• Coordinate with clinical research personal for preparation of ICF and CRF
2 Ethics submission :
• Coordinate with the investigator for submitting the study related documents (clinical updated) to independent Ethics Committee.
3 Subject Recruitment/ Screening :
• Coordinate with screening team for subject recruitment & screening.
4 Study Related :
• Coordinate with clinical research personal for of Protocol.
• Coordinate with clinical research personal for preparation of ICF and CRF
2 Ethics submission :
• Coordinate with the investigator for submitting the study related documents (clinical updated) to independent Ethics Committee.
3 Subject Recruitment/ Screening :
• Coordinate with screening team for subject recruitment & screening.
4 Study Related :
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