Regulatory Affairs Consultant

Há 5 dias


Sao Paulo, Brasil Parexel Tempo inteiro

timely performance of work within a project scope to the quality expectations of PC and the client. When serving as a Project Lead or Work Stream Lead, a consultant secures the work of the entire team or work stream is delivered on time and that it meets client’s and PC’s quality.

**Skills and knowledge**:
Regulatory Affairs Consultant should have solid local expertise in submitting Clinical Trials to Health Authority in Brazil.
This role will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in Brazil. Also, will coordinate and manage flow of information, track project progress, and identify and solve problems in a team-oriented environment.

Good communication and leadership skills as well as team player attitude is needed to be successful in this position. Detail orientation and flexibility will be highly appreciated as well.



  • Sao Paulo, Brasil Parexel Tempo inteiro

    **Skills and knowledge**: Regulatory Affairs Consultant should have solid local expertise in submitting Clinical Trials to Health Authority in Brazil. This role will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in Brazil. Also, will coordinate and manage flow of information, track...


  • São Paulo, São Paulo, Brasil Parexel Tempo inteiro

    **Skills and knowledge**:Regulatory Affairs Consultant should have solid local expertise in submitting Clinical Trials to Health Authority in Brazil.This role will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in Brazil. Also, will coordinate and manage flow of information, track project...


  • São Paulo, São Paulo, Brasil Parexel Tempo inteiro

    timely performance of work within a project scope to the quality expectations of PC and the client. When serving as a Project Lead or Work Stream Lead, a consultant secures the work of the entire team or work stream is delivered on time and that it meets client's and PC's quality.**Skills and knowledge**:Regulatory Affairs Consultant should have solid local...


  • São Paulo, São Paulo, Brasil beBeeRegulatoryAffairs Tempo inteiro US$60.000 - US$95.000

    Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with all relevant laws and regulations.About the RoleThe successful candidate will have a strong background in regulatory affairs, with experience in...


  • São Paulo, São Paulo, Brasil beBeeregulatory Tempo inteiro R$80.000 - R$120.000

    Regulatory Affairs SpecialistThe position supports the Brazil Regulatory Affairs group to prepare submission and registration documents for new or existing product offerings.Key Responsibilities:Regulatory affairs support.Documentation management.Database maintenance.Submission preparation.This role requires strong organizational skills, attention to detail,...


  • São Paulo, São Paulo, Brasil beBeeRegulatoryAffairs Tempo inteiro R$60.000 - R$90.000

    About Regulatory Affairs RolesWe are seeking an experienced professional to fill a key regulatory affairs position in São Paulo, Brazil.Job Responsibilities:Assess regulatory requirements for clients' products in Brazil and ensure compliance.Prepare and submit regulatory submissions to Brazilian regulatory authorities.Provide guidance on regulatory...


  • São Paulo, São Paulo, Brasil beBeeregulatory Tempo inteiro R$40.000 - R$80.000

    We are currently seeking a skilled Regulatory Affairs Specialist to support the development and approval of our pharmaceutical products. This is an exciting opportunity for someone with experience in regulatory affairs and a strong knowledge of local regulations.Key responsibilities will include ensuring compliance with all relevant regulations,...


  • São Paulo, São Paulo, Brasil beBeeProfessional Tempo inteiro R$80.000 - R$120.000

    Regulatory Affairs ProfessionalWe are seeking a skilled Regulatory Affairs professional to fill this challenging role in Brazil.

  • Regulatory Affairs Expert

    2 semanas atrás


    São Paulo, São Paulo, Brasil beBeeCompliance Tempo inteiro US$150.000 - US$200.000

    Regulatory Affairs Expertise in BiopharmaceuticalsWe are seeking a skilled Regulatory Affairs Associate Director to lead our biopharmaceutical regulation process, ensuring seamless compliance with target country legislation and efficient execution.This role will play a pivotal part in supporting our global strategy on regulatory matters, fostering...


  • Sao Paulo, Brasil Serviap Group Tempo inteiro

    Responsible for planning and implementing the strategy for medical devices registration activities for clients - Support in responding to RFPs for regional regulatory projects - Responsible for planning, executing, and coordinating all regulatory activities including major lifecycle maintenance and customer’s market expansion activities - Able to manage...