Chennai

Bachelors degree in nursing, Life Sciences, Biomedical Engineering, or related field. Clinical background in nephrology or dialysis is highly desirable

To effectively review visit reports as per Protocol and ICON and Sponsor SOPs and to ensure the quality of reports are of the highest standards , errors are minimized and that issues are escalated as appropriate

Conduct laboratory trials and formulation/process evaluation. Support aseptic processing and sterile manufacturing development. Evaluate formulation parameters and excipient compatibility.

Create and maintain detailed data management plans and documentation, ensuring compliance with industry standards and regulatory requirements.

relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions

Bachelor Degree in Pharmacy Allopathic OR Doctor of Pharmacy from a Central or State Government recognized University invited for working at central government, railways, RRB

Ph.D. degree holders are eligible to apply within five years of completion of Ph.D.  2. Age limit: Maximum 32 years by the date of joining. Relaxation of 5 years for SC/ST and women candidates, and 3 years for OBC-NCL candidates. 

Execution of CMC strategies for Pfizer Global Supply (PGS) initiated prioritized post approval changesglobally in collaboration with the CMC GRS.

Preparing and submitting comprehensive safety reports, including periodic safety update reports and individual case safety reports in compliance with regulatory standards.