Title:  Publications Coordinator (PC)

Date:  Feb 6, 2025
Location: 

NJ, US

Jan 2024

Publication Coordinator

 

Responsibilities and key activities include but are not limited to:

 

Publication Process Support (including in Phoenix)

  • Support product publication teams with data entry and record updates in Phoenix and Papers
  • Create new Document records in Phoenix as needed or take ownership of converted Documents within 24 hours of creation
  • Coordinate with writers and subject matter experts to ensure timely circulation and delivery of publication materials
  • Proactively manage individual publication timelines and drive adherence to key milestones, including regular follow-ups with stakeholders and maintenance of document milestones in Phoenix
  • Participate in publication strategy and writer meetings to maintain currency of publication records 
  • Schedule and conduct publication status meetings with SMEs, writers, SAPMs, and GPPLs, as needed
  • Ensure accurate, consistent metadata in Phoenix; perform data cleanup as needed
  • Maintain an up-to-date knowledge of SOP, best practices, product team dynamics, and other outlined processes 
  • Ensure publication compliance and adherence to the Publications SOP
  • Document author eligibility in accordance with the Publications SOP and ICMJE criteria
  • Proactively request letters of agreement (LOAs) for new authors and send follow-up reminders as needed
  • Route all full-scope publications for author review and final author approval and ensure author responses are appropriately documented in Phoenix
  • Perform required compliance checks and route all full-scope and FPR-only publications for Final Publication Review (FPR), ensuring that the appropriate reviewers and assigned and all reviewer feedback is appropriately documented in Phoenix
  • Escalate potential compliance issues and exceptions as identified 
  • Assist with manuscript/abstract submission upon request
  • Ensure final versions of all GP3 publication, along with appropriate metadata, are appropriately archived in Papers
  • Maintain QRGs and reference documents as they relate to PC activities

 

Basic Qualifications

  • Bachelor's degree and 2 years of professional experience

OR

  • Associate’s degree and 5 years of professional experience

OR

  • High school diploma I GED and 7 years of professional experience

 

Preferred Qualifications

  • Experience in the pharmaceutical, biotechnology, or other healthcare-related field.
  • Ability to work with a diverse group of stakeholders across multiple time zones in a timely and professional manner.
  • Demonstration of strong attention to detail.
  • Strong ability to work independently but also as part of cooperative team.
  • Excellent verbal and written communication skills; strong interpersonal skills.
  • Demonstrated time management and decision-making skills with the ability to triage and prioritize time-sensitive tasks.
  • Strong organizational, problem-solving, and multi-tasking abilities.
  • Quick and proactive learner.
  • Proficient experience with project management tools, methodologies, and practices.
  • Experience organizing and coordinating multiple projects with many variables and managing shifting timelines.
  • Experience with MSOffice, Excel, SharePoint, and Webex.
  • Previous editorial experience a plus.
  • Ability to be flexible and adapt to changing timelines.
  • Ability to think creatively and take initiative.