Document and Analytics Specialist - SSP
Princeton, NJ
About the Job
12 months to start contract
Princeton, NJ
Pharma domain
Role Requirement
Document management and control:
Analytics:
Qualifications
Required:
Preferred:
Princeton, NJ
Pharma domain
Role Requirement
Document management and control:
- Create document numbers in the Veeva Vault system and route documents for approval
- Manage document development (concept-publication) by logging activities in the MS Teams project tracking spreadsheet.
- Meet with authors (as needed) to facilitate updates and scale the updates into Inkling,
- Create and maintain support docs for corporate policies and SOPs, such as forms, spreadsheets, and .pdfs.
- Adhere to all project timelines and commitments.
Analytics:
- Create and manage reports for business owners and leadership using the Tableau platform.
- Support the development and execution of the analytics strategy related to Otsuka documentation. This includes providing data driven insights and recommendations.
Qualifications
Required:
- 2 years + experience creating and maintaining digital documents in Inkling (or other CMS)
- 3 years of professional experience in Pharma or other regulated environment
- 1 + years of experience using Tableau, Power BI or other analytics platform to interpret data and create reports
- Strong project management and follow-through skills
- Ability to juggle multiple projects and priorities simultaneously and work with all levels of management
- Excellent communication skills; needs to be able to collaborate with various stakeholders at all levels of mgmt
Preferred:
- Ability to create and maintain support documents such as MS Word forms, spreadsheets, and .pdfs
- Experience working in the MS Teams environment
- An understanding of the steps involved with the lifecycle of a document such as moving a document from concept through publication (concept, creation, approvals, build, publication, and documentation)
Source : SSP