TRABAJO CLINICAL REGULATORY MANAGER BARCELONA, BARCELONA

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

The position will involve conducting mechanistic pbpk using clinical data to support the clinical development of drug candidates across therapy areas...

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

Training / strong knowledge on good clinical practices... experience: 2-3 years of experience in a clinical research management... extensive knowledge of all steps...

This is what you will do: assist the cpls for the planning, implementation, execution and compliance of operational plans for clinical study/program with multiple...

You will need to have: 2 years of clinical research experience or course-work equivalent in clinical research... serving as a content manager for study-specific...

We want to be the clinical research organisation that delivers excellence to our clients and to patients at every touch-point... y ou will be adding value through...

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

clinical input to nda/bla)... prepare and provide input to clinical study reports (csrs) and clinical portions of regulatory documents (e...

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

Engage with clinical investigators on clinical studies to enable quality clinical execution, analyze and interpret clinical data, and collaborate with the broader...

Accountable for the clinical strategy and clinical execution of a portfolio of pre-clinical and clinical stage therapies... the candidate will lead all regulatory...

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...

As regulatory professionals working on oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life-changing treatments...

Please, check out our recruitment policy the role   we are seeking an enthusiastic project manager to join our team...   interview: preselected candidates will...

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