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Regulatory Affairs Consultant

extra holidays - extra parental leave - fully flexible
Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

More than 6 years in Clinical Trial Regulatory, Experience leading global regulatory projects, Knowledge of EU-CTR 536/2014 preferred, Project management knowledge, Proficiency in local language.

Key responsabilities:

  • Support global strategies and ensure compliance
  • Coordinate submission of Core dossiers
  • Manage flow of information and problem-solving
  • Review technical documents for regulatory compliance
  • Interface with project teams and regulators
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Parexel Pharmaceuticals XLarge http://www.parexel.com/
10001 Employees
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

We are currently recruiting for two Regulatory Affairs Consultant / Leads roles, one located in Mexico and the other located multi-country (Argentina o Peru or Brazil). As Regulatory Affairs Consultant / Leads, these individuals will play a pivotal role in supporting our global strategies and ensuring compliance with local regulations in their respective regions.

Skills and experience:

  • More than 06 years in the Clinical Trial Regulatory Area.
  • Having experience in leading projects at the global regulatory level.
  • Having experience leading the regulatory team and coordinating the compilation of the Core dossiers to be submitted by the SMEs to several countries worldwide from end to end.
  • Experience in Central America countries will be value, but it's not mandatory.
  • Knowledge of EU-CTR 536/2014 (ideal).
  • Coordinate and manage the flow of information, track project progress, and identify and solve problems in a team-oriented environment.
  • Reviews of critical key technical documents (e.g. clinical trial protocols and reports, study drug labels, and other clinical trial-related technical documentation) to ensure regulatory compliance for clinical trial applications, consistency with other key documents and ease of review.
  • Interface with the project team and the regulatory authorities on regulatory and technical matters, as appropriate.
  • Support the sponsor for the development of optimized clinical trial submission strategies.
  • Project management knowledge.
  • Advanced written and Speaking English.
  • Client-focused approach to work.
  • Results orientation.
  • Teamwork and collaboration skills Consulting skills.
  • Excellent interpersonal and intercultural communication skills, both written and verbal.
  • Critical thinking and problem-solving skills.
  • Proficiency in the local language.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
EnglishEnglish
Check out the description to know which languages are mandatory.

Other Skills

  • Problem Solving
  • Teamwork
  • Consulting
  • Interpersonal Communications
  • Critical Thinking

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