Direct message the job poster from GForce Life Sciences
Riley O'Connor
Executive Recruiter at GForce Life Sciences
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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