TRABAJO REGULATORY AFFAIRS LEAD STUDY MADRID, MADRID

Colaborar con el regulatory affairs manager y con el regulatory affairs head, aportando la información necesaria para realizar el seguimiento del presupuesto asociado...

Reports study progress/update to the global study associate director/ global study team including smm lead... collaborates with local medical affairs team...

· regulatory compliance (change control, post-approval activities, etc... )· interactions with key business partners and regulatory authorities· launch or supply...

Participate in or lead projects to maximize team effectiveness i... experience with health care, business national/ regional legislative and executive branch regulatory...

In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; e... as a subject matter expert, the medical strategy lead will...

Biology, chemistry, biochemistry, pharmacology) with a minimum of 10 years of experience in biocides regulatory affairs...    lead cross-geographical forums to facilitate...

At least 8 years experience working in public policy and government affairs... your role will focus on understanding local regulatory landscapes and driving impactful...

Everyday blends operational focus, regulatory problem-solving, and cross-functional coordination... you’ll gain exposure to various therapeutic areas and clinical...

Implementation of study amendment-and changes in study related processes)... as required, manages the local study supply... drive study compliance by maintaining...

Provide legal advice in close coordination with the senior lead counsel italy-iberia for strategic issues... plan and deliver training programs, including on align...

Able to lead taskforces and provide innovative input... • develop integrated study management plans with the core project team... • manage risk (positive and negative)...

Able to lead taskforces and provide innovative input... • lead the study management team including providing updates to all trial team members on deliverable status...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

•    in-depth knowledge of european pricing mechanisms and regulatory frameworks (e...     •    establish and maintain strong relationships with external stakeholders...

As a core clinical trial team (ctt) member, you'll lead critical aspects of global studies and collaborate across functions to drive success...

Compliance & regulatory affairs  design and oversee the company’s compliance framework, policies, and internal controls... this includes building and leading...

Advise on regulatory interactions, support successful management of regulatory examinations and requests; conduct regulatory horizon scanning...