Document Management Specialist
Document Management Specialist
GForce Life Sciences
New Jersey, United States
See who GForce Life Sciences has hired for this role
Global Document Management Specialist
Our client, a growing, mid-sized pharmaceutical client is seeking a Global Document Management Specialist to manage medical affairs Veeva Vault submissions and approvals.
Responsibilities:
- Manage global medical affairs Veeva Vault (MedComms/PromoMats) submissions and approvals
- Assist with global medical & training slide kit resource development
- Responsible for providing editorial support, ensuring the quality of content, with a focus on accuracy and consistency of slide kits developed by Medical Affairs before Veeva submission for PRC or MRC review.
- Complete the required content annotations, reference checking & tagging in Veeva MedComms/PromoMats
- Ensures all pieces are grammatically and factually correct and comply with AMA style
- Completes required copy editing & formatting of slide kits and medical resources
- Assumes accountability for the accuracy of work
- Complete all resource development/approval tracking & documentation
Education and Experience:
- Master Degree Required
- 1-3 years agency pharma slide kit content development experience is required
- Familiarity working with Veeva PromoMats/MedComms data management & submissions
Term & Start
- 12+ month contract with the possibility to extend
- Remote
- Healthcare benefits available
- 2 weeks to start from offer
-
Seniority level
Associate -
Employment type
Contract -
Job function
Administrative and Quality Assurance -
Industries
Medical Equipment Manufacturing, Biotechnology Research, and Pharmaceutical Manufacturing
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See who you knowFeatured Benefits
Inferred from the description for this job
-
Medical insurance -
Dental insurance -
Vision insurance -
401(k)
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