TRABAJO REGULATORY AFFAIRS MANAGER CLINICAL BARCELONA, BARCELONA

This role is the key account manager for the regulatory eu marketing company (eumc) thereby managing and coordinating all eu regulatory affairs cp-related matters...

The global study manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance... support the study team in the implementation...

More than 10 years of regulatory affairs experience experience in global regulatory strategy and submissions that have progressed through to registration...

• direct the study team in the implementation of audits and regulatory inspections... • oversee the clinical trial insurance process; track approvals, revisions...

Communication with regulatory authorities... plan, create, analise and/or review medical devices clinical investigation documents... if you love to take new challenges...

The rid will work closely with therapeutic area (ta) vp, executive regulatory science directors, global regulatory leaders (grls) and regulatory affairs directors...

Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... understanding of scientific and clinical...

The clinical research medical advisor is a global clinical development role with medical responsibility for the clinical trial process...

The associate director study leader, early oncology clinical is responsible for the delivery of clinical studies including quality, timelines, budgets, resources...

• extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities in clinical study management processes and clinical/drug...

clinical development... • at least 5 years’ experience mainly in a clinical safety department or closely related areas e... • support the management and oversight...

You will be responsible for supporting business relationships with defined stakeholder groups in development, regulatory and safety and for the delivery of risk...

A good understanding of global regulatory requirements for clinical trials and document management and/or experience with clinical trial management systems and patient...

• knowledge of clinical trials - knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements, i...

Quality:  ensure awareness and compliance with applicable standard operating procedures to meet, comply and champion all quality and regulatory commitments of boston...

Description: is the leader of the project team and responsible for collaboration with assigned team in meeting client deliverables as outlined in the contract responsible...

The manufacturing project manager contributes to the execution of the regional manufacturing strategy by managing a broad variety of projects within and across the...

clinical input to (s)nda/(s)bla)... implement clinical r&d policies, sops and related directives... prepare various official and regulatory documents for regulatory...