400,000 - 500,000 INR 
Full Time
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Skills
"CRA" "Report Writing" "Clinical Research Associate" "Protocol Writing" "SOPs" "GCP guidelines"- Experience
- 3 to 5 Years
- Industry
- Pharma / Biotech / Life Science
- Functional Area
- Other
Job Description
- 1. Responsible for overall conduct of the BE study from literature search to clinical study report writing.
- 2. Ensure that the study conduct and data handling comply with Protocol.
- 3. Developing,writing, implementing and maintaining standard operating procedure
Desired Candidate Profile
- 1. Ensure conduct of the study as per the standards laid down in the SOPs.
- 2. Ensure timely conduct of clinical trials and comply with GCP guidelines, SOPs and applicable regulatory.
- Company
- Konnect HR Executive Search Firm
- Location
- Konnect HR Executive Search Firm
Kalwa (W) - Website
- http://konnecthr.com/
- View Jobs By This Company
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