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Clinical Study Portfolio and Publication Manager

Job in South San Francisco, San Mateo County, California, 94083, USA
Listing for: Veracyte
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Healthcare Administration, Healthcare Management
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the Veracyte way its about how we work together, guided by our values, to give clinicians the insights they need to help patients make life‑changing decisions.

Our Values:

  • We Seek A Better Way
    :
    We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care
  • We Make It Happen
    :
    We act with urgency, commit to quality, and bring fun to our hard work
  • We Are Stronger Together
    :
    We collaborate openly, seek to understand, and celebrate our wins
  • We Care Deeply
    :
    We embrace our differences, do the right thing, and encourage each other
The Position:

Responsible for maintaining metrics and data across the clinical trial portfolio while coordinating and tracking scientific publications. This role combines data management with publication process oversight to support clinical and medical affairs.

Responsibilities:
  • Develops and maintains comprehensive metrics tracking systems for clinical trial portfolio data
  • Monitors and coordinates scientific publication activities from initiation through submission and publication
  • Manages manuscript submission process, ensuring compliance with journal requirements and internal guidelines
  • Creates and updates trial data dashboards to provide real‑time visibility into portfolio performance
  • Supports authors and research teams throughout the manuscript development process, including timeline management and resource coordination
  • Performs quality control checks to ensure data accuracy and consistency across the clinical trial portfolio
  • Establishes and maintains effective communication channels between clinical teams, medical affairs, and other stakeholders
  • Generates regular progress reports and analytics to inform strategic decision‑making and track portfolio performance
  • Implements and maintains publication tracking systems to monitor status, deadlines, and deliverables
  • Coordinates with internal teams to gather necessary data and documentation for publication submissions
  • Identifies and resolves data discrepancies across portfolio documentation
  • Provides regular updates to leadership on portfolio metrics and publication status
Publication Coordination:
  • Track status of scientific publications from inception to completion
  • Coordinate manuscript reviews and submission processes as needed
  • Maintain publication planning timeline
  • Monitor publication deadlines and deliverables
  • Maintain master schedule of conferences and submission deadlines
Administrative:
  • Organize and maintain documentation
  • Schedule and coordinate publication‑related meetings
  • Prepare status updates for leadership
  • Maintain publication tracking databases
  • Support manuscript development process
Who You Are:

Required Qualifications:
  • Bachelor's degree in life sciences, healthcare, or related field
  • 6–7 years experience in clinical research or publications
  • Strong data analysis and management skills
  • Proficiency in MS Office and data visualization tools
  • Experience with Veeva Vault Clinical Trial Management System
  • Excellent organizational and communication skills
Preferred Qualifications:
  • Advanced degree in relevant field
  • Experience with publication management software
  • Knowledge of medical publishing requirements
  • Understanding of clinical research processes
  • Project management certification
  • Experience with data analytics tools
Skills:
  • Attention to detail
  • Strong analytical abilities
  • Project management
  • Time management
  • Communication
  • Problem‑solving
  • Database management
  • Statistical analysis

This role requires a combination of analytical skills and coordination abilities to effectively manage both data and publication workflows.

#LI‑Hybrid

The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to years of experience, skillset, geographic location, industry, education, etc. Base pay is one part of the Total Package that is…

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