Vagas na beBeeRegulatory em Brasil

Job Title: Regulatory Affairs Specialist · We are seeking a skilled and experienced regulatory affairs specialist to oversee local submissions for observational studies across Brazil, Argentina, and Chile. · ...

Key Job Responsibilities · The role of a Regulatory Affairs Specialist is critical to ensure quality, consistency and timeline adherence across multiple locations. · Gather relevant documentation for local submissions; · Evaluate compliance with international clinical trial regul ...

Regulatory Affairs Manager · The Regulatory Affairs Specialist will provide centralized oversight and execution of local submissions across three countries to ensure quality, consistency, and timeline adherence. · <ol style= ...

Regulatory Compliance Specialist Job Description · The role provides centralized oversight and execution of local submissions across multiple markets to ensure quality, consistency, and timeline adherence. · Manage regulatory submissions and site start-up activities ensuring comp ...

Regulatory Affairs Specialist Role · Are you a seasoned professional in Regulatory Affairs seeking a new challenge? Do you have expertise in medical device classification and regulatory compliance? · <ol style= ...

Regulatory Affairs Expert · We are seeking a highly skilled Regulatory Affairs expert to lead our medical device regulatory activities. This role will involve ensuring compliance with European regulations and working closely with cross-functional teams. · ...

Freelance Regulatory Specialist · We are seeking a freelance regulatory specialist to oversee local submissions across three countries, ensuring quality, consistency and timeline adherence. · Manage regulatory submissions and site start-up activities. · Ensure compliance with int ...

We are seeking a regulatory affairs professional to manage the submission process for observational studies in Latin America. · Key Responsibilities: · Oversee the planning and execution of site start-up activities · Ease compliance with international clinical trial regulations t ...

Regulatory Affairs Career Opportunity · This is a key role for someone with experience in medical device regulatory affairs, ideally working with Class IIa and IIb devices. · About the Role · The primary focus of this position is to lead Regulatory Affairs activities for medical ...

Upsilon Global is seeking a freelance regulatory and start-up specialist with solid experience in Ethics Committee submissions for observational studies. The role will provide centralized oversight and execution of local submissions to ensure quality, consistency, and timeline ad ...

Job Title: · Regulatory Affairs Specialist · Freelance Regulatory & Study Start-Up Opportunity in LATAM · The role will provide centralized oversight and execution of local submissions across the three countries to ensure quality, consistency and timeline adherence. · [Start Date ...

Job Opportunity: · We are seeking a highly skilled freelance regulatory specialist to manage submissions and site start-up activities across three countries in LATAM. This role will provide centralized oversight and execution of local submissions, ensuring quality, consistency, a ...

Upsilon Global are seeking a freelance regulatory specialist to oversee local submissions in LATAM, specifically Chile, Argentina and Brazil. · The role will provide centralized oversight and execution of local submissions across the three countries to ensure quality, consistency ...

Freelance Regulatory & Study Start-Up Specialist · The role of this position is to provide centralized oversight and execution of local submissions across multiple countries, ensuring quality, consistency and timeline adherence. · Manage regulatory submissions and site start-up a ...

Seeking a Regulatory Affairs Specialist to provide centralized oversight and execution of local submissions across three countries in LATAM. · About this role · <ul style= ...

We are seeking a highly skilled regulatory specialist to oversee the execution of local submissions across Chile, Argentina and Brazil. · The role will provide centralized management and coordination of regulatory activities to ensure quality, consistency and timeline adherence. ...

Regulatory Affairs Specialist Position · This role involves overseeing and executing local submissions for observational studies in infectious diseases across key regions. · Spearhead regulatory submissions, including site start-up activities. · Evaluate compliance with regulator ...

Job Description: · As a Regulatory Affairs Specialist, you will lead activities for medical devices ensuring compliance with EU regulations. This role involves acting as an expert in Class IIa and Class IIb devices. · Key Responsibilities: · Coordinate the preparation, review, ma ...

Regulatory Compliance Expert · The primary objective of this role is to oversee regulatory activities for medical devices, ensuring seamless alignment with European regulations (EU MDR – Regulation (EU) 2017/745). This encompasses acting as an authority on medical device classifi ...

Regulatory Affairs Professional Role · This role focuses on ensuring adherence to European regulations, particularly the EU MDR. You will lead regulatory affairs activities for medical devices. · Responsibilities: · Demonstrate expertise in leading projects related to EU MDR and ...