TRABAJO REGULATORY AFFAIRS MANAGER CLINICAL BARCELONA, BARCELONA

Desirable requirements basic understanding of clinical trials methodology... at morgan philips, we are looking for a knowledgeable clinical data manager to join...

Locally main contact are the clinical operations manager 3 and 4, study manager and study lead monitors...   value added: the clinical project support specialist...

What you’ll do the global clinical operations program director (gpd) is a core global role within the haematology  r&d clinical operations function...

The csa collaborates closely with the project manager country operations (pmco) and other local study team members in com such as study start up (ssu) manager...

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

 drive the necessary processes to ensure 100% compliance with all regulatory requirements and be a key support for internal and external audits and inspections...

Create collaborative relationships with other functional areas and internal stakeholders including, but not limited to, global medical affairs operations, sales...

We are seeking a dynamic and experienced  product manager  to join our team and lead the product management of our cutting-edge electronic medical records (emr)...

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...

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

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

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...

Deliver clinical sessions and presentations on  disease state, drugs, clinical studies and other scientific topics to diverse audiences, including kols, hcps, and...

Working in collaboration with the obu medical excellence teams, global medical affairs leaders, and field medical leaders to provide strategic direction, implement...

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...