TRABAJO CLINICAL SITE ENGAGEMENT BARCELONA, BARCELONA

Essential skills/experience: relevant clinical or biomedical ph... job title: director clinical scientist, oncology r&d, early clinical location: barcelona, spain...

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

Excellent communication and stakeholder engagement abilities... data transformation: leverage data tools and strategies to transform and enhance r&d and clinical...

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

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

This fill-time (40 hours) role, is planned for 11 months and is to support the site in barcelona in conducting a clinical trial in the field of cardiology...

Msc in clinical trials monitoring... ensure compliance with the protocol, good clinical practices (gcps), and clinical trial regulations... maintain consistent communication...

• support activities associated with company-sponsored site quality audits and regulatory authority inspections... the gsa operates in accordance with the rare disease...

Proven expertise in cmo/cdmo engagement and successful contract negotiations... the ideal candidate will have extensive experience in cmo/cdmo environments, drug...

€¢ *to acquire knowledge of ich gcp, the conduct of clinical trials and governing regulations, relevant icon sops, icon internal tracking systems and client sops...

clinical input to (s)nda/(s)bla)... implement clinical r&d policies, sops and related directives... they share responsibility with clinical operations team members...

clinical input to nda/bla)... accountable for the clinical and scientific leadership and integrity of protocols, clinical study reports and/or components of clinical...

Ensuring site selection process is conducted by identifying potential sites/investigators, performing initial site quality risk assessment, and conducting site qualification...

clinical trial management system)... with clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our...

’ this role is working in our core clinical site management function... next generation clinical development! as a cra you will receive an ipad and use of key developments...

' this role is working in our core clinical site management function... next generation clinical development! as a cra you will receive an ipad and use of key developments...

The ta lead represents sm&m in various cross functional optimisation and engagement workstreams... the role sits within oncology site management and monitoring within...

Responsibility:review and approve analytical documentation, including coa, site master file, sops, and product specifications... take part in certifying investigational...