Opening for Cross Functional Data Analyst Bengaluru/Bangalore @ PPD Pharmaceutical
Key Responsibilities As a Cross Functional Data Liaisons, you will use a combination of tools and analytical techniques to detect, investigate, diagnose, and mitigate risk within clinical trials more efficiently and accurately from a global perspective. You will be in charge of analysing operational and patient clinical trial data to identify and characterize issues and trends that can be indicators of project risk. You will blend an analytic approach with cross-function operational knowledge to evaluate and communicate issues to the appropriate functional team members for further investigation and resolutions. You will serve as an advocate for early risk mitigation and corrective action by reporting and effectively communicating across global business units project data risks. Qualification: BA/BS degree in computer science, statistics, biostatistics, mathematics or related field. 2 years of statistics, programming, clinical trial research, and/or quality principles experience. Must have database management, SAS or PL/SQL programming experience. Prior experience in clinical monitoring, data management or related environment in support of clinical trials Broad working knowledge of the roles, functions and process of conducting clinical trials Broad grasp of medical/therapeutic area knowledge and of medical terminology Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations Ability to effectively review and evaluate operational and clinical trial data Strong analytical and intuitive skills with the ability to shift perspective between detail-oriented and big-picture views
Desired Candidate Profile Education: UG -Any Graduate - Any Specialization, Graduation Not Required
Click here to apply
Key Responsibilities As a Cross Functional Data Liaisons, you will use a combination of tools and analytical techniques to detect, investigate, diagnose, and mitigate risk within clinical trials more efficiently and accurately from a global perspective. You will be in charge of analysing operational and patient clinical trial data to identify and characterize issues and trends that can be indicators of project risk. You will blend an analytic approach with cross-function operational knowledge to evaluate and communicate issues to the appropriate functional team members for further investigation and resolutions. You will serve as an advocate for early risk mitigation and corrective action by reporting and effectively communicating across global business units project data risks. Qualification: BA/BS degree in computer science, statistics, biostatistics, mathematics or related field. 2 years of statistics, programming, clinical trial research, and/or quality principles experience. Must have database management, SAS or PL/SQL programming experience. Prior experience in clinical monitoring, data management or related environment in support of clinical trials Broad working knowledge of the roles, functions and process of conducting clinical trials Broad grasp of medical/therapeutic area knowledge and of medical terminology Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations Ability to effectively review and evaluate operational and clinical trial data Strong analytical and intuitive skills with the ability to shift perspective between detail-oriented and big-picture views
Desired Candidate Profile Education: UG -Any Graduate - Any Specialization, Graduation Not Required
Click here to apply
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