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Sr/Regulatory Affairs Specialist - FSP - EMEA

Role overview

Qualifications

  • Bachelor's degree/previous experience comparable to 2+ years
  • Good English language (written and oral) communication skills
  • Good attention to detail and quality as well as editorial/proofreading skills
  • Good interpersonal skills to work effectively in a team environment

Responsibilities

  • Review country essential documents for completeness, accuracy, and quality as defined by the Essential Document Compliance (RDC) checklist.
  • Review site essential documents for completeness, accuracy, and quality as defined by the Essential Document Compliance (RDC) checklist.
  • Notify EDP Submitter via email of review outcome detailing requested revisions and/or corrected documents when deficiencies are noted.
  • Track EDP review details in the applicable data tracking system.

Key facts

  • Remote from: EMEA
  • Full time
  • Senior (5-10 years)
  • Regulatory Affairs Specialist
  • English

Hard skills

Other skills

  • Detail Oriented
  • Critical Thinking
  • Social Skills
  • Computer Literacy
  • Microsoft Word
  • Microsoft Excel
  • Microsoft PowerPoint
  • Communication
  • Teamwork
  • Organizational Skills
  • Time Management
  • Planning

About the company

Thermo Fisher Scientific logo

Thermo Fisher Scientific

Biotechnology

About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.

Company details

IndustryBiotechnology
Company size10001

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Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Regulatory Affairs Specialist – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to serve as the lead over several countries/projects in providing innovative solutions, including regulatory expertise and client interface. As a Regulatory Affairs Specialist, you will beresponsible for the review and approval of country- and site-level essential documents required for site activation. The documents required for each study site and country are documented in a study-specific Essential Document Compliance (EDC) Review Checklist. Once final study documents are available, the Regulatory Affairs Specialist reviews all required essential regulatory documentation for completeness, accuracy and quality, ensuring that documentation meets applicable regulatory and study requirements and supports timely site activation.

What You’ll Do:

  • Review country essential documents for completeness, accuracy, and quality as defined by the Essential Document Compliance (RDC) checklist. 

  • Review site essential documents for completeness, accuracy, and quality as defined by the Essential Document Compliance (RDC) checklist. 

  • Notifies EDP Submitter via email of review outcome detailing requested revisions and/or corrected documents when deficiencies are noted. 

  • Review revised packs to ensure deficiencies were resolved and communicate review outcome to the SSU Specialist. 

  • Tracks EDP review details in the applicable data tracking system. 

  • Maintain knowledge and understanding of SOPs, client SOPs/directives, and current regulatory guidelines. 



Education and Experience Requirements:

  • Good English language (written and oral) communication skills as well as local language where applicable 

  • Good attention to detail and quality as well as editorial/proofreading skills 

  • Good interpersonal skills to work effectively in a team environment 

  • Good computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies 

  • Basic organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects 

  • Good negotiation skills 

  • Capable of working independently with direction and exercising independent judgment 

  • Bachelor's degree/previous experience comparable to 2+ years 

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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