Thermo Fisher Scientific

Thermo Fisher Scientific

Posted via Workday

SSU

Posted Sep 3, 2026

Role at a glance

Salary
Not Disclosed
Location
Shanghai, China
Work arrangement
On-site
Employment
Full-time
Experience
Proven experience in regulatory submission processes.

Spotted an issue?

We’ll check it against the original posting.

Log in to report

Role Summary

AI-generated

Coordinates country-level regulatory and ethical submissions and related site start-up activities. The role supports local submission strategy, site activation, and maintenance of trial and study documentation.

What You'll Do

  • Prepare, review, and coordinate local regulatory submissions in alignment with global submission strategies.
  • Provide local regulatory strategy advice and project-specific local SIA services, and serve as a country-level contact for submission...
  • Coordinate site start-up activities with internal departments to align with submission timelines and support site activation targets.
  • Assist start-up CRAs with regulatory compliance review packages and develop country-specific patient information and informed consent...
  • Support grant budget and payment schedule negotiations with sites and coordinate feasibility activities.
  • Maintain trial status information in tracking databases and prepare, set up, and maintain local country study files.

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

Proven experience in regulatory submission processes; organizational and coordination skills; ability to collaborate; communication skills for interacting with investigators and internal clients; attention to detail and determination to deliver flawless results.

Required

  • Proven experience in regulatory submission processes.
  • Outstanding organizational and coordination skills.
  • Ability to work collaboratively in an ambitious and innovative environment.
  • Strong communication skills to interact with investigators and internal clients.
  • Strict attention to detail and determination to deliver flawless results.

Original job description

Content provided by the employer

Work Schedule

Environmental Conditions

Job Description

Job Description

At Thermo Fisher Scientific, you have the chance to contribute to groundbreaking research that positively impacts the world. Our mission is to enable our customers to make the world healthier, cleaner, and safer. We support our teams with the essential resources to reach their career goals while advancing science through research, development, and delivery of transformative therapies. Join us in a role that drives meaningful change and improves health outcomes globally!

Responsibilities

  • Prepare, review, and coordinate local regulatory submissions under mentorship to align with global submission strategies.
  • Provide local regulatory strategy advice (MoH &/or EC) to internal clients.
  • Offer project-specific local SIA services and coordination.
  • Serve as a key contact at the country level for Ethical or Regulatory submission activities.
  • Coordinate with internal departments to ensure site start-up activities align with submission timelines.
  • Achieve PPD’s target cycle times for site activation.
  • Assist start-up CRAs in preparing regulatory compliance review packages.
  • Develop country-specific Patient Information Sheet/Informed Consent form documents.
  • Support grant budget and payment schedule negotiations with sites.
  • Coordinate feasibility activities in accordance with agreed timelines.
  • Enter and maintain trial status information on PPD tracking databases accurately and timely.
  • Ensure local country study files are prepared, set up, and maintained per PPD WPDs or applicable client SOPs.
  • Maintain knowledge of PPD SOPs, Client SOPs/directives, and current regulatory guidelines.

Requirements

  • Proven experience in regulatory submission processes.
  • Outstanding organizational and coordination skills.
  • Ability to work collaboratively in an ambitious and innovative environment.
  • Strong communication skills to interact with investigators and internal clients.
  • Strict attention to detail and determination to deliver flawless results.

Benefits

We offer competitive remuneration, an annual incentive plan bonus, comprehensive healthcare, and a range of employee benefits. Working with Thermo Fisher Scientific means joining an innovative, forward-thinking organization with outstanding career and development prospects. Our exciting company culture stands for integrity, intensity, involvement, and innovation. Join us and be part of a team that values diverse experiences and perspectives!

Thermo Fisher Scientific

About the company

Thermo Fisher Scientific

Large Enterprise

Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.