Arun Kuna Email & Phone Number | Overseeing the case handling, triage and processing of clinical trial and spontaneous postmarketing events. Assisting in the management and analysis of safety data with a particular emphasis on support to clinical development teams, and helps define the pharmacovigilance needs of clinical development teams, advising and providing guidance to clinical development teams on safety matters. Take part in the review and input in investigator brochure content, expert reports, and pooled study data. Review and evaluate individual adverse events/reactions. Perform initial assessments of cases, review and modify case narrative. Participation in the reconciliation between the Clinical Trial Database and the pharmacovigilance database to ensure quick and complete data validation. Assist with trial end activities in preparation for clinical study report. Provide input in the review of the safety aspects of study protocols and reports. Case approval for non-serious, non-reportable cases after data entry is complete. Case unblinding at trial termination. Specialties: Drug Safety and Epidemiology Pre-Clinical and Clinical Pharmacology (Cardiovascular research) Clinical Pharmacokinetics and Pharmacodynamics

Arun Kuna

Overseeing the case handling, triage and processing of clinical trial and spontaneous postmarketing...
Thane, Maharashtra, India

*50 free lookup(s) per month.

Arun Kuna’s Email akuna@labcorp.com

Arun Kuna’s Phone Numbers

Get ARUN’s Phone Number (For Free)

Social Media

Arun Kuna’s Location Thane, Maharashtra, India

Arun Kuna’s Current Industry Labcorp Drug Development

Arun Kuna’s Prior Industry Covance | Novo Nordisk | Quintilesims

Find accurate emails & phone numbers for over 700M professionals.

Asst Manager(Ic), Safety Sciences

2018-05-01 00:00:00 - Present

Senior Drug Safety Associate Pv Dss-Apac

2015-04-01 00:00:00 - 2018-04-01 00:00:00

Drug Safety Professional

2014-01-01 00:00:00 - 2015-03-01 00:00:00

Senior Drug Safety Associate

2012-10-01 00:00:00 - 2013-12-01 00:00:00

No Skills Available

No Languages Available

Arun Kuna is a Overseeing the case handling, triage and processing of clinical trial and spontaneous postmarketing events. Assisting in the management and analysis of safety data with a particular emphasis on support to clinical development teams, and helps define the pharmacovigilance needs of clinical development teams, advising and providing guidance to clinical development teams on safety matters. Take part in the review and input in investigator brochure content, expert reports, and pooled study data. Review and evaluate individual adverse events/reactions. Perform initial assessments of cases, review and modify case narrative. Participation in the reconciliation between the Clinical Trial Database and the pharmacovigilance database to ensure quick and complete data validation. Assist with trial end activities in preparation for clinical study report. Provide input in the review of the safety aspects of study protocols and reports. Case approval for non-serious, non-reportable cases after data entry is complete. Case unblinding at trial termination. Specialties: Drug Safety and Epidemiology Pre-Clinical and Clinical Pharmacology (Cardiovascular research) Clinical Pharmacokinetics and Pharmacodynamics