Regulatory Affairs Associate - CONSULTANT
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
ClinChoice is searching for a Regulatory Affairs Associate Consultant for 12 months Contract with possibility of extension to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Job Title: Regulatory Affairs Associate - CONSULTANT
Location: Mexico; Remote
Responsibilities:
Support planning and project management across Regulatory Affairs, serving as the key liaison with global stakeholders
Leverage data analytics, metrics, and insights to organize regulatory information, demonstrate value, and enable informed decision-making across the business
Collect, review, and upload product, licensed product and license data in databases (e.g., UDI, eligibility, etc.)
Review, execute and drive eligibility releases as per required procedures
Review, track and monitor critical Notified Body mailbox and invoices
On a project/product basis, facilitate change orders for DEC/DoC/DD and other documents in the PLM system(s), and assist with strategy creation, follow-up on local assessments and creation of relevant documentation (e.g., letters to file)
Maintain/update in all relevant databases and sources (e.g., GRID for document self-serve)
On a project basis, monitor, track and execute regulatory operational processes as required
Perform other tasks as required
Minimum Requirements:
Bachelor’s degree (life sciences preferred)
Knowledge of EU MDD/MDR, ISO13485, US FDA QSR
Proven ability to manage and track multiple regulatory projects and timelines
Strong data analytics skills with experience using metrics, dashboards, and reporting to drive decisions and demonstrate value
Proficient in Microsoft Office (e.g., Word, Excel, PowerPoint)
Strong proficiency in written and verbal English communication is required.
Key Words: Regulatory Affairs, data analysis, EU MDD, EU MDR, ISO 13485, US FDA QSR
#LI-PB1 #LI-REMOTE
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Regulatory Affairs Associate - CONSULTANT
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
ClinChoice is searching for a Regulatory Affairs Associate Consultant for 12 months Contract with possibility of extension to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
Job Title: Regulatory Affairs Associate - CONSULTANT
Location: Mexico; Remote
Responsibilities:
Support planning and project management across Regulatory Affairs, serving as the key liaison with global stakeholders
Leverage data analytics, metrics, and insights to organize regulatory information, demonstrate value, and enable informed decision-making across the business
Collect, review, and upload product, licensed product and license data in databases (e.g., UDI, eligibility, etc.)
Review, execute and drive eligibility releases as per required procedures
Review, track and monitor critical Notified Body mailbox and invoices
On a project/product basis, facilitate change orders for DEC/DoC/DD and other documents in the PLM system(s), and assist with strategy creation, follow-up on local assessments and creation of relevant documentation (e.g., letters to file)
Maintain/update in all relevant databases and sources (e.g., GRID for document self-serve)
On a project basis, monitor, track and execute regulatory operational processes as required
Perform other tasks as required
Minimum Requirements:
Bachelor’s degree (life sciences preferred)
Knowledge of EU MDD/MDR, ISO13485, US FDA QSR
Proven ability to manage and track multiple regulatory projects and timelines
Strong data analytics skills with experience using metrics, dashboards, and reporting to drive decisions and demonstrate value
Proficient in Microsoft Office (e.g., Word, Excel, PowerPoint)
Strong proficiency in written and verbal English communication is required.
Key Words: Regulatory Affairs, data analysis, EU MDD, EU MDR, ISO 13485, US FDA QSR
#LI-PB1 #LI-REMOTE