Job Details
Responsibilities:
Develop and maintain client relationships and highlight opportunities for increased service support to the respective lead.
Good understanding and participation in regulatory processes providing high-level Regulatory Informatics & Operations support in dossier Modules 1 to 5 for all applicable document types and Health Authority regions. Supporting pre-publishing, dossier compilation, dossier publishing and post-publishing activities.
Good understanding and participation in regulatory processes providing high-level Regulatory Informatics & Operations support for informatics related Health Authority initiatives
Good understanding and working knowledge of US and EU eCTD submissions across all submission types.
Veeva Tool knowledge is preferred.
to be able to work in CET/US shift timezone.
Qualification:
B.Pharm or other Science degree, M.Pharm preferred
Experience:
Minimum 3 years of experience
Skills & Knowledge:
Submission publishing (mandatory) US Publishing experience
Veeva tool experience (preferred) Veeva Publishing experience
Flexibility:
Must be open to working in shifts if required
Schedule
Full time
Affiliated Companies
Affiliated Companies: PharmaLex India Private Limited
Equal Employment Prospect
Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.
The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consiste