Submission Readiness Document Manager

Posted 3 Hours Ago
Be an Early Applicant
Grania, Barcelos, Braga, PRT
In-Office
46K-86K Annually
Mid level
Biotech • Pharmaceutical
The Role
Ensure clinical documents are submission-ready and compliant with regulatory requirements. Oversee technical editing/formatting, implement templates and processes, manage vendors, resolve operational issues, support audits/inspections, and drive continuous improvements across global teams.
Summary Generated by Built In

Salary Range:

€46,300.00 - €86,100.00

Job Description Summary

Job Title: Submission Readiness Document Manager
#LI-Hybrid
Primary Location: Barcelona, Spain
Relocation Support: This role is based in Barcelona Gran Via, Spain. Novartis is unable to offer relocation support: please only apply if accessible.
Ready to play a critical role in delivering life-changing medicines to patients worldwide? As a Submission Readiness Document Manager, you will ensure that clinical documents are technically compliant, and submission-ready—enabling timely and accurate regulatory submissions. You’ll collaborate across global teams, drive process improvements to enhance clinical document management systems, processes and standards at Novartis. This role offers a unique opportunity to shape how clinical documents support regulatory success while strengthening operational excellence across a fast-paced, global environment.

Job Description

Key Responsibilities
  • Manage submission-readiness of clinical documents, ensuring compliance with regulatory requirements and quality standards
  • Oversee technical editorial and formatting of clinical documents for regulatory submissions
  • Ensure clinical documentation meets Health Authority guidelines, Good Clinical Practice, and Novartis procedures
  • Support implementation of submission readiness strategies and standardized document templates
  • Collaborate with cross-functional teams to deliver high-quality documents within timelines
  • Monitor vendor performance, track service metrics, and drive continuous improvement initiatives
  • Act as escalation point for submission readiness issues and resolve operational challenges
  • Identify risks, trends, and gaps in submission processes and implement appropriate mitigations
  • Serve as Subject Matter Expert for submission readiness processes, tools, and training materials
  • Support audits and inspections, including root cause analysis and corrective and preventive actions
Essential Requirements
  • Bachelor’s degree in life sciences, healthcare, pharmacy, or information management
  • Proven experience in clinical development, clinical operations, or a similar environment (3–5 years)
  • Strong expertise in clinical document management processes and regulatory requirements
  • Advanced knowledge of documentation best practices, including data integrity and good documentation principles
  • Experience working with document management systems and strong understanding of system structures and functionality
  • Ability to manage projects in a global, cross-functional environment
  • Strong organizational, tracking, and communication skills
  • High level of independence with the ability to manage complex priorities effectively
 

Benefits & Rewards 

 

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. 

  

Expected Annual Base Salary Range for role: 46,300 to 86,100 EURO

  

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. 

  

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. 

  

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. 

  

Read our brochure to learn more about our global total rewards offering: 

  

https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf 

  

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process. 

 

Commitment to Diversity and Inclusion / EEO paragraph 

Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve. 


 

Skills Desired

Budget Management, Clinical Trials, Process Improvements, Project Planning, Vendor Management, Waterfall Model

Skills Required

  • Bachelor's degree in life sciences, healthcare, pharmacy, or information management
  • Proven experience in clinical development, clinical operations, or similar environment (3-5 years)
  • Strong expertise in clinical document management processes and regulatory requirements
  • Advanced knowledge of documentation best practices, including data integrity and good documentation principles
  • Experience working with document management systems and strong understanding of system structures and functionality
  • Ability to manage projects in a global, cross-functional environment
  • Strong organizational, tracking, and communication skills
  • High level of independence with the ability to manage complex priorities effectively
  • Budget Management
  • Clinical Trials
  • Process Improvements
  • Project Planning
  • Vendor Management
  • Waterfall Model

Novartis Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Novartis and has not been reviewed or approved by Novartis.

  • Healthcare Strength Pay and benefits are described as a strong overall package, supported by medical, dental, and vision insurance alongside FSAs/HSAs and disability and life coverage. Mental-health support is reinforced through an employee assistance program with psychological support and a network of mental health first aiders.
  • Retirement Support Retirement support is positioned as a standout element, with an automatic company contribution plus dollar-for-dollar matching in the 401(k). Additional retirement funding is described through an age-based defined contribution program and access to an employee share purchase plan discount.
  • Parental & Family Support Family-related benefits are framed as robust, including a global minimum of paid parental leave for new parents following birth or adoption. Added supports include domestic partner coverage, dependent-care resources, and benefits such as adoption assistance and child/elder care options.

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The Company
HQ: Basel
110,000 Employees
Year Founded: 1996

What We Do

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.

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