GForce Life Sciences

Document Management Specialist

GForce Life Sciences New Jersey, United States

Direct message the job poster from GForce Life Sciences

Riley O'Connor

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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