CHINOIN Private Co, Ltd Posted October 21, 2026

Regulatory Project Coordinator Supporting Trainee

Budapest, Hungary Part time
Notify me about similar jobs

CHINOIN Private Co, Ltd is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Location: Budapest – Sanofi Budapest HUB, Váci Greens

About the job

Looking to launch your career at the cutting edge of healthcare? Join Sanofi for a chance to develop with mentoring and guidance from inspirational leaders while helping to make an impact on the lives of countless people worldwide.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main responsibilities:

Deliver key start and follow-up of submissions, initial/HA Request for Supplementary Information as per plan/requests for Sanofi products including EU and US submissions

Coordination of administrative and regulatory activities in Veeva Vault RIM system, monitor and follow-up the team's KPI dashboard, tracking systems

Applying simplification of the end-to-end processes and retrieve information from regulatory database and regional regulations

Maintenance and improvements of the current regulatory repositories already in place

Participate to the preparation and update of quality document, processes, tool enhancement and training materials pertaining to role

Monitor KPI’s by running reports, collating data and report as per oversight and governance process

About you

Experience:

BSc or MSc university studies in Life Sciences (active student status for minimum 12 months) in Hungary

25 -hour availability/week

 Soft and technical skills:

Strong interest in EU and US regulatory affairs, any basic academic exposure to regulatory frameworks is a plus

Willingness to learn how electronic systems and regulatory databases are used in pharmaceutical environments

Curiosity about regulatory dossiers and their structure (e.g., eCTD format)

Attention to detail and ability to support tracking of regulatory activities in internal systems

Openness to working in a cross-functional and multicultural team setting

Strong organizational skills and eagerness to support activities requiring planning and coordination

Ability to collaborate in a highly matrixed, fast-paced environment

 Languages: Strong written and verbal communication skills in English

Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Budapest, Hungary
Employment type
Part time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 589 comparable Regulatory Affairs roles across 114 biopharma companies.

589Comparable roles tracked
544Currently active
114Companies hiring similar roles
53Countries represented

Salary context

157 of 589 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $75,038 – $380,750 (median $186,375)

Where these roles are based

Top locations among the 589 comparable roles

United States236
India47
Japan34
United Kingdom33
Poland27
Ireland20

+ 47 more countries

Seniority mix

456 of 589 peers have a known seniority level

Manager181
Director73
Senior59
Associate Director55
Intern/Fellow/Postdoc25
Senior Director23
Principal17
Associate13
Executive/VP10

Therapeutic area mix

44 of 589 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology14
Immunology10
Rare Disease6
Dermatology & Aesthetics5
Vaccines & Infectious Disease3
Neuroscience3
Cardiovascular / CVRM2
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

25%similar
Lilly Shanghai, Shanghai, China Associate Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie Maidenhead, ENGLAND Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie Mettawa, IL Associate Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

Open in 3 locations

North Chicago, United StatesFlorham Park, United StatesWaltham, United States
25%similar
AbbVie Associate Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

Open in 2 locations

Irvine, United StatesNorth Chicago, United States

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Regulatory Affairs job in Hungary, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

25%
Regulatory Affairs Associate Director
Lilly · Shanghai, Shanghai, China · Associate Director
Function Therapeutic area Seniority Country
25%
Director, RA Global Regulatory Strategy
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
25%
Director, RA Global Regulatory Strategy
AbbVie · Florham Park, NJ · Director
Function Therapeutic area Seniority Country
25%
Associate Director, Regulatory Affairs US & Canada Strategy Lead – Facial Aesthetics - Device
AbbVie · North Chicago, IL · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.