Job Description:
Responsible for the production, quality and functionality of specific content sets. Participates in specialist interpretation in the form of research, analysis, and writing to support the development and maintenance of clinical trial information in all media, and ensures that published information contains premium content.
Responsible for the production, quality and functionality of specific content sets. Participates in specialist interpretation in the form of research, analysis, and writing to support the development and maintenance of clinical trial information in all media, and ensures that published information contains premium content.
Roles & Responsibilities:
• Responsible for the curation & analysis of clinical trials content from various sources such as trial registries, press releases, scientific meetings, conferences, etc.
• Maintain good quality standards
• Content analysis from scientific posters and abstracts.
• Able to write abstracts
• Responsible for the curation & analysis of clinical trials content from various sources such as trial registries, press releases, scientific meetings, conferences, etc.
• Maintain good quality standards
• Content analysis from scientific posters and abstracts.
• Able to write abstracts
Interview Rounds:
1st round: Written test (Technical - Topics mentioned above)
2nd round: Interview discussion (Technical)
1st round: Written test (Technical - Topics mentioned above)
2nd round: Interview discussion (Technical)
Additional Information
Experience: 1 - 3 years
Location: Chennai, Hyderabad
Educational Qualification: M.Pharm / M.Sc Chemistry, Biochemistry
Functional Area : Analyst
End Date : 30th November, 2018
Experience: 1 - 3 years
Location: Chennai, Hyderabad
Educational Qualification: M.Pharm / M.Sc Chemistry, Biochemistry
Functional Area : Analyst
End Date : 30th November, 2018
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