Exciting opportunity at Chennai Pfizer Regulatory Affairs Operations (CDM) team!
Inviting applications from Regulatory Affairs operations professionals experienced in Data Management
RA Operations Date Management:
To function as Team Lead, CDM Global Regulatory Operations and responsible for managing a team of data management in a focused manner, ensure timely updates in requatory systems, esclations, business process etc… Manage data associates and interface, Collaborate with
functionally responsible roles. Regionally focused data management oversight & workload management
Contribute to evolving data management and serve as a change agents with regional contact. Lase with regional BU strategists, coordinate the ssues of the reports and metrics.
Responsible for develop and enhance the capabilities and capacities of the Single Charinel of Communication (SCC) team throughout the identification and implementation of training and development needs.
Support Regional Cluster Lead as Change Agent and roll out system, tools implementing and adaptation
Technical Skills:
Linderstanding of the concepts around regulatory activities Understanding of regional regulatory requirements. Articulate with analytical and interpersonal skills. Proven aptitude in project management and process redesign. Knowledge of local regulatory environment and how this impacts regulatory strategy and knowledge of drug development practise, rules, regulations and guidelines
Experience: 3-5 Years in People management Data
management. Regulatory information management (RIM) Submission management etc. in Global Regulatory Affairs (Operations)
M.Pharm and or Lifesciences degree plus relevant experience is preferred.
Interested candidates can apply to the role of Team Lead. CDM (4845678) via LinkedIn or send your updated resume to [email protected]
