TRABAJO REGULATORY AFFAIRS CLINICAL WRITING BARCELONA, BARCELONA

• represent clinical regulatory writing on cross-functional teams and advocate and train teams in authoring and review best practice... the clinical regulatory writing...

Key member of  the clinical study team...   participating in safety review meeting regarding potential safety events within a given clinical study or ac ross the...

Collaborating in global initiatives to standardize processes within and across countries (collaboration with other local and global csas) assist with local language...

Prepare regulatory documentation and design processes with the quality and regulatory affairs teams to comply with the artificial intelligence regulation and other...

Pre-process process and analyze data from clinical trials including demographic clinical and device usability data... prepare regulatory documentation and design...

Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...

Pharmacovigilance), clinical research, or regulatory affairs solid knowledge in drug safety related processes (incl... supports all clinical trial activity and post...

Conditions: duration:  1 year hours per day:  full time location:  barcelona focus areas:    opportunities across different teams such as research & development...

Pricing centre of excellence collaborate closely with market access & government affairs teams to build evidence that helps optimize pricing and market access on...