As part of the Clinical Data and Information Sciences CDIS group an integral delivery unit within the Clinical Development Operations CD O organization the Clinical Data Scientist is responsible for representing CDIS at the study team level The Clinical Data Scientistis accountable for the coordination of all CDIS deliverables associated with a clinical trial as well as adherence to data standards and the quality of the study data sets The Clinical Data Scientist provides leadership direction and oversight to Data Managers working on the clinical trial and is accountable for the trials inspection readiness Serve as Clinical Data Scientist for one or more clinical trials assuming responsibility for all CDIS activities including selection and application of data acquisition standards Data Management Plan selection of quality risk indicators third party study data due diligence As a member of the Core Study Team drive operational excellence in collaboration with crossfunctional partners through the application of CDIS best practices at the study level serve as technical resource on how to best collect process consume and report clinical trial data They are accountable for the quality and timeliness of all CDIS deliverables in support of the clinical trial They partner with Research Business Units external data service providers and internal CDIS staff to deliver highquality data management for all studies as assigned Proactively drives quality and efficiency to meet study asset timelines milestones ensuring scientific and operational excellence in support of strategic imperatives and in collaboration with the cross functional study team Ensure work carried out by on behalf of CDIS is in accordance with applicable SOPs and work practices accountable for assuring adherence to regulations standards GCDMPs ALCOA principles by the team they are coordinating Ensure the required studyspecific CDIS documents in the Trial Master File TMF are of high quality and are filed contemporaneously Work with Asset Leads to establish strategy timelines and adequate resourcing of the study Provide leadership direction and oversight to the CDIS resources working on the clinical trial s Work Location Assignment On Premise Pfizer is an equal prospect employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates To learn more about acceptable and prohibited uses of AI during the recruitment process please review our candidate AIuse guidelines available on Pfizer Careers Medical

📌 Clinical Data Scientist Manager Clinical Data and Information Sciences (Chennai)
🏢 Pfizer
📍 Chennai