Post COVID , during back to office it will be required to move to Client location Bridgewater, NJ. As he/she needs to work with customer closely. But for now this is fine to continue from present location as in next 6 months or so , it will be work from home only.
1. Fair knowledge on Regulatory Affairs ( Submission Content Planning) business process
2. Strong hands on experience on Veeva Configuration and Architecting the solution
3. Ability to configure and build new Veeva Configuration modules
4. Understand the existing Veeva Configuration / code and update as per the requirement changes.
5. Knowledge of Veeva RIM modules like Document Management, Registration Management, xEVMPD , Dossier Management , Application , Submission etc are required.
6. Knowledge on other Vault like Vault eTMF, Vault Promomats etc is good to have but not mandatory.
7. Experience in Veeva SDK Code development ( Good to Have)
8. Excellent communication kills
9. Ability to work on extra hours on need basis.
10. Good team player and a great team leader Need to lead the team technical and derive the solution. Deliver customer requirements on time with proper quality standard.
11. Knowledge of writing Functional Specification, Design Specification, Test Scripts is must.
12. Knowledge of Service Now, JIRA and HP ALM is added advantage
13. Other than Regulatory domain knowledge, having knowledge on Clinical Domain adds extra mileage.
14. Good to have – experience in working in Agile methodology.