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 trial’s inspection readiness.
- 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 high-quality 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 study-specific 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 opportunity employer and complies with all applicable equal employment chance legislation in each jurisdiction in which it operates.

Medical

📌 Manager, Clinical Data Scientist (Chennai)
🏢 Pfizer
📍 Chennai