NextRaiseNextRaiseFind jobs
Sign inSign up free
Jobs
8 days ago
Apply with autofill
Apply with autofill
Thermofisher·8 days ago
8 days ago

Sr/Regulatory Affairs Specialist - FSP - EMEA

Sofia, BulgariaFull-timeRemoteSenior · 5-8 yearsRegulatory Affairs Specialist

Sign up free to see how well your resume matches this role.

Boost your chances at thermofisher

How you compare FREE

?
Your scoreYour score: not yet known
→
27
Top 10%Top 10%: 27 out of 100

Top 10% of NextRaise users, across all roles in this function in Bulgaria.

Must-have skills for this role

  • regulatory affairs
  • essential documents
  • document review
  • edc

PDF or DOCX · no account needed

Apply faster with autofill FREEThe NextRaise extension autofills your application in one click.careers.example.com/applyAutofillingFull namePriya SharmaEmailpriya.sharma@example.comPhone+49 30 1234567LocationBerlGet the extension

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.

What they're looking for

  • 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

Summarised by NextRaise from the employer’s description, which follows in full below.

Full description from employer

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 be responsible 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 

Company

Thermofisher
Sofia, Bulgaria

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from Thermofisher's careers site·first seen 15 Sept 2026·last verified 15 Sept 2026·How we source jobs

Similar jobs

  • Sr/Regulatory Affairs Specialist - FSP - EMEA at Thermo Fisher ScientificSofia, Bulgaria–match not yet calculated
  • Senior Regulatory Compliance Specialist at nexoSofia, Bulgaria–match not yet calculated

Browse more jobs

  • Regulatory Affairs Specialist jobs in United States
  • Regulatory Affairs Specialist jobs in United Kingdom
  • Regulatory Affairs Specialist jobs in India
  • Retail Sales Associate jobs in United States