DIRECTOR SAFETY REGULATORY AFFAIRS jobs in ILLINOIS, United Kingdom

and regulatory requirements. Assess safety of environment and take the initiative to help prevent accidents and promote safety... Director of Clinical Operations to join our new start-up territory! The ideal candidate will be within a 45-minute commute...

Professional Case Management

Director, Medical Affairs will serve as one of the internal medical affairs experts for the USMA function and medical... and scientific input to the pharmacovigilance group (may serve as member of the safety committee) regulatory documents...

Lundbeck

systematically defines quality objectives, both strategic and applicable regulatory requirements. Director, Safety, Regulatory... and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA...

AbbVie

systematically defines quality objectives, both strategic and applicable regulatory requirements. Director, Safety, Regulatory... and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA...

AbbVie

systematically defines quality objectives, both strategic and applicable regulatory requirements. Director, Safety, Regulatory... and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA...

AbbVie

because the work we do matters. Join us! Job Summary The Director, Deputy General Counsel, Regulatory Affairs is responsible... for providing legal opinions on matters related to the regulatory, safety and economic frameworks applicable to CN in the United...

Canadian National Railway

because the work we do matters. Join us! Job Summary The Director, Deputy General Counsel, Regulatory Affairs is responsible... for providing legal opinions on matters related to the regulatory, safety and economic frameworks applicable to CN in the United...

Canadian National Railway

is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides... inspections with safety, RA or MA in scope. The role reports to the Senior Director of Safety, Vigilance and Medical Affairs...

AbbVie

is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides... inspections with safety, RA or MA in scope. The role reports to the Senior Director of Safety, Vigilance and Medical Affairs...

AbbVie

strategically with Global Regulatory Strategy and Safety to maintain an accurate safety profile for assigned products. Provides... of these documents with changing regulatory environments. Mentors and educates cross-functional team members concerning global...

AbbVie

strategically with Global Regulatory Strategy and Safety to maintain an accurate safety profile for assigned products. Provides... of these documents with changing regulatory environments. Mentors and educates cross-functional team members concerning global...

AbbVie

responsibility for routine and ad hoc safety monitoring reports to regulatory agencies. May review, assess and report applicable... (i.e., commercial, clinical operations, discovery, statistics, regulatory, etc…) as they relate to on-going medical affairs projects...

AbbVie

responsibility for routine and ad hoc safety monitoring reports to regulatory agencies. May review, assess and report applicable... (i.e., commercial, clinical operations, discovery, statistics, regulatory, etc…) as they relate to on-going medical affairs projects...

AbbVie

on , , , and . Job Description Purpose: The Associate Medical Director provides specialist medical/scientific strategic and operational input into core... medical affairs activities within their TA inclusive of healthcare professional/provider interactions; generation of clinical...

AbbVie

on , , , and . Job Description Purpose: The Associate Medical Director provides specialist medical/scientific strategic and operational input into core... medical affairs activities within their TA inclusive of healthcare professional/provider interactions; generation of clinical...

AbbVie

to the regulatory authorities. Participation in design and execution of clinical trial safety, product safety and risk... management plans. May also carry responsibility for routine and ad hoc safety monitoring reports to regulatory agencies. May...

AbbVie

regulatory authorities. Participation in design and execution of clinical trial safety, product safety and risk management plans.... May also carry responsibility for routine and ad hoc safety monitoring reports to regulatory agencies. May review, assess...

AbbVie