Would you like to join and contribute to a successful and growing multi-national organization in the heart of Europe and one of the world’s leading regions of the pharmaceutical industry?

• Leading regulatory activities on assigned projects
• Develop and lead regulatory strategy
• Ensuring regulatory compliance of assigned projects
• Independent preparation of regulatory dossiers
• Interactions with Health Authorities
• Interactions with client contact persons
• Coaching junior team members

What we do

For more than 27 years, Veristat has built a reputation as global experts in clinical development.

• 760+ Rare Disease Clinical Trials supported
• 160+ Marketing Applications supported
• In 2022 we supported 8 marketing application that received regulatory approval
• Learn more about our core values here!

What we offer

• The estimated hiring range for this role is 120K – 150K CHF plus applicable bonus. This hiring range is specific to Switzerland and will vary for other regions based upon local market data.  Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.
• Benefits vary by location and may include:
  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for

• Master/PhD in Pharmacy, Life Sciences or equivalent
• Minimum of 8 years regulatory affairs experience in in consulting or pharmaceutical industry
• Experience with early development projects, including PIPs, ODDs, authority meetings and MAAs under the centralized procedure
• Global regulatory experience is a plus
• Excellent communication skills
• Fluent in English; German

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.