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Publications Lead

Dawar Consulting

ApplySave Job
  • Date Posted

    Yesterday

    New!
  • Remote Work Level

    100% Remote

  • Location

    Remote, US Nationalicon-usa.png

  • Salary

    $81 - $81 HOURLY

  • Benefits

    Health/Medical Insurance Paid Sick Leave Paid Vacation

  • Categories

    Healthcare,  Pharmaceutical,  Publishing,  Product Manager,  Project Manager,  Research,  Writing

  • Job Type

    Freelance

  • Career Level

    Manager

  • Travel Required

    No Specification

  • Education Level

    Ph.D., MD

About the Role

Title: Publications Lead (100% Remote)

Location: San Mateo, California, 94404, United States

Job Information

  • Job Opening ID3468
  • Job TypeLong-Term Contract
  • LocationFoster City, CA
  • IndustryPharma
  • CitySan Mateo
  • State/ProvinceCalifornia
  • CountryUnited States
  • Zip/Postal Code94404
  • Number of Positions1
  • Work ExperienceAny

Department: Pharma

Job Description:

Our client, a world leader in biotechnology and life sciences, is looking for a “Publications Lead (100% Remote)”.

 

Job Duration: Long Term Contract (Possibility of Extension)

Pay Rate: $81/hr on W2

 

Company Benefits: Medical, Paid Sick leave(as per state policy)

 

Responsible for leading and executing scientific publication activities across cell therapy programs within a pharmaceutical or biotechnology organization. Manages end-to-end publication development, including manuscripts, abstracts, posters, and presentations, while ensuring scientific quality, compliance, and timely delivery.

 

Key Responsibilities

  • Lead publication planning and execution across manuscripts, abstracts, posters, and presentations.
  • Manage publications from initial planning through submission and post-publication activities.
  • Coordinate with Medical Affairs, Clinical, HEOR, investigators, authors, and external experts.
  • Oversee medical writing agencies, review deliverables, and manage timelines and risks.
  • Maintain publication trackers, calendars, and documentation.
  • Ensure compliance with ICMJE, GPP, and internal publication policies.
  • Support multiple therapeutic programs and take ownership of ongoing projects with minimal onboarding.

 

Required Qualifications

  • Advanced degree in Life Sciences: PhD, PharmD, MD, or MSc.
  • 5–7+ years of medical publications experience within pharma or biotech.
  • Strong knowledge of ICMJE and GPP publication guidelines.
  • Experience managing publication projects, external vendors, and cross-functional stakeholders.
  • Excellent project management, prioritization, communication, and attention to detail.

 

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