TRABAJO CLINICAL SITE TRIALS CONTRACT BARCELONA, BARCELONA

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

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

It is a bridge between study site operations (sso) clinical trials and medical affairs, aligning technical, operations & strategy... summary clinical research medical...

Msc in clinical trials monitoring... advanced knowledge of gcps and clinical trials legislation... breast cancer clinical trials experience will be an asset...

contract and inventory management: establish and maintain an inventory of r&d & clinical platform components, including their corresponding contracts and...

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical...

• support activities associated with company-sponsored site quality audits and regulatory authority inspections... • provide administrative support to global study...

Icon plc is a world-leading healthcare intelligence and clinical research organization... as a dmpm, you will manage a global team of clinical data management resources...

€¢ *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 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... join us in our exciting journey!! we currently require a motivated, creative and enthusiastic...

' this role is working in our core clinical site management function... join us in our exciting journey!! we currently require a motivated, creative and enthusiastic...

Responsible for driving standardization within smm in conduct of feasibility, site selection, operational projections and processes... maintains awareness of marketplace...

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

The role • to review and negotiate clinical site investigator contracts and budgets... study start up associate / contract specialist at icon, it’s our people...

The role: • to review and negotiate clinical site investigator contracts and budgets... icon plc is a world-leading healthcare intelligence and clinical research...

Analyse data from routine information systems, national-level surveys and clinical trials to contribute to genomic surveillance activities in mozambique and quantify...