What are the responsibilities and job description for the Global Document Management Specialist position at GForce Life Sciences?
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's 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
- Pay Range - up to 40hr
