TRABAJO CLINICAL ASSOCIATE II SITE BARCELONA, BARCELONA

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

Re-trains site personnel as appropriate • conducts continuous site monitoring activities (onsite and remote)... • performs site initiation visit, ensures site personnel...

site training plan, site monitoring plan, cross functional data review plan, ip release plan etc... this is what you will do: assist the cpls for the planning, implementation...

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

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

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

Present results of data gathering and analysis activities undertake therapeutic training, as necessary, and keep abreast of developments in clinical research train...

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 (s)nda/(s)bla)... possesses detailed knowledge of good clinical practice (gcp) and other regulations governing clinical research...