Manager, Clinical Data Scientist, Cdis (Tamil Nadu)

Job Description

ROLE SUMMARY As part of the Clinical Data Sciences CDS group an integral delivery unit within the Clinical Development Operations CD O organization the Clinical Data Scientist CDS is responsible for timely and high-quality data management deliverables supporting the Pfizer portfolio The CDS delivers asset level information strategies and services for optimal use and reuse of internal and external information that will advance research development and commercialization of the Pfizer portfolio and further precision medicine The CDS designs develops and maintains key data management deliverables used to collect review monitor and ensure the integrity of clinical data applies standards data review and query management and is accountable for quality study data set release and consistency in asset submission data ROLE RESPONSIBILITIESServe as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDS activities including selection and application of data acquisition standards Data Management Plan selection of quality risk indicators third party study data due diligence Serve as a technical resource to the study teams for DM and RBM standards tools data provisioning and reporting Partners with Research Business Units external DM service providers and internal CDS staff to deliver high quality data management for all studies as assigned Proactively drives quality and efficiency to meet timeline and milestones for data management ensuring scientific and operational excellence in support of strategic imperatives and in collaboration with the cross functional study team s Ensure work carried out by or on behalf of CDS is in accordance with applicable SOPs and working practices Participates and ensures quality database design including documentation testing and implementation of clinical data collection tools both CRF and non-CRF using an electronic data capture EDC system and or other data collection systems Ensure the required study specific CDS documents in the Trial Master File TMF are of high quality and are filed contemporaneously Ensure operational excellence in collaboration with partners for application of standards data acquisition proactive data review and data integrity monitoring data cleaning e-data processing data access and visualization and database release Work Location Assignment Hybrid Pfizer is an equal chance employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates Medical ROLE SUMMARY As part of the Clinical Data Sciences CDS group an integral delivery unit within the Clinical Development Operations CD O organization the Clinical Data Scientist CDS is responsible for timely and high-quality data management deliverables supporting the Pfizer portfolio The CDS delivers asset level information strategies and services for optimal use and reuse of internal and external information that will advance research development and commercialization of the Pfizer portfolio and further precision medicine The CDS designs develops and maintains key data management deliverables used to collect review monitor and ensure the integrity of clinical data applies standards data review and query management and is accountable for quality study data set release and consistency in asset submission data ROLE RESPONSIBILITIESServe as Clinical Data Scientist and Trial Lead for one or more clinical trials assuming responsibility for all CDS activities including selection and application of data acquisition standards Data Management Plan selection of quality risk indicators third party study data due diligence Serve as a technical resource to the study teams for DM and RBM standards tools data provisioning and reporting Partners with Research Business Units external DM service providers and internal CDS staff to deliver high quality data management for all studies as assigned Proactively drives quality and efficiency to meet timeline and milestones for data management ensuring scientific and operational excellence in support of strategic imperatives and in collaboration with the cross functional study team s Ensure work carried out by or on behalf of CDS is in accordance with applicable SOPs and working practices Participates and ensures quality database design including documentation testing and implementation of clinical data collection tools both CRF and non-CRF using an electronic data capture EDC system and or other data collection systems Ensure the required study specific CDS documents in the Trial Master File TMF are of high quality and are filed contemporaneously Ensure operational excellence in collaboration with partners for application of standards data acquisition proactive data review and data integrity monitoring data cleaning e-data processing data access and visualization and database release Work Location Assignment Hybrid Pfizer is an equal chance employer and complies with all applicable equal e

Keyskills :
Clinical Data ManagementClinical TrialsQuery ManagementElectronic Data CaptureData Acquisition StandardsData Management PlanQuality Risk IndicatorsData ReviewData Set Release