IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
Post : Consultant
Job Description
Clinical coding and clinical support for site identification and optimization
Clinical coding and clinical support for site identification and optimization
Responsibilities:
• Identify right set of ICD diagnosis and procedure codes/NDC based on trial protocol
• Identify/rank clinical sites based on research on drug usage - posology
• conversion of data to patient equivalents and DoT
• Desk research on epidemiology
• Identify potential clinical investigators based PUBMED analytics/social media/patient load/conferences
• Identify right set of ICD diagnosis and procedure codes/NDC based on trial protocol
• Identify/rank clinical sites based on research on drug usage - posology
• conversion of data to patient equivalents and DoT
• Desk research on epidemiology
• Identify potential clinical investigators based PUBMED analytics/social media/patient load/conferences
Candidate Profile
• MBBS/B.Pharm/M.Pharm,Graduate/PG in Biotechnology, Graduate/PG in other lifesciences and Paraclinical fields
• Clinical coding experience is a must
• Ability to synthesize information from the validated sources for assessing the (given) market by unmet needs, current treatment trends, key analogues for prototyping, market sizing, emerging algorithms and impact analysis
• Good understanding of clinical trial mapping activities with respect to the therapy area knowledge, patient segments, biomarkers, protocol designs, endpoints and dosing/strengths used for evaluation
• Secondary research capabilities
• Background in dealing with pharma data
• Strong written and oral communication
• Ability to convert analysis to visual format in excel/power pointAdditional Information
Qualification : MBBS/B.Pharm/M.Pharm• MBBS/B.Pharm/M.Pharm,Graduate/PG in Biotechnology, Graduate/PG in other lifesciences and Paraclinical fields
• Clinical coding experience is a must
• Ability to synthesize information from the validated sources for assessing the (given) market by unmet needs, current treatment trends, key analogues for prototyping, market sizing, emerging algorithms and impact analysis
• Good understanding of clinical trial mapping activities with respect to the therapy area knowledge, patient segments, biomarkers, protocol designs, endpoints and dosing/strengths used for evaluation
• Secondary research capabilities
• Background in dealing with pharma data
• Strong written and oral communication
• Ability to convert analysis to visual format in excel/power pointAdditional Information
Location : Bangalore
Industry Type: Pharma/ Healthcare/ Clinical research
Functional Area: Consultant
End Date : 25th September, 2018
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