TRABAJO CLINICAL SITE SPECIALIST MEDICAL BARCELONA, BARCELONA

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

Serve as the medical expert for clinical study team... engage with clinical investigators on clinical studies to enable quality clinical execution, analyze and interpret...

• early oncology clinical delivery... • understanding of early phase clinical delivery... we are seeking a director study leader rtsm specialist in early oncology...

clinical input to (s)nda/(s)bla)...   the global development medical director plays a critical role in the medical monitoring of a clinical study ensuring safety...

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

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

The senior medical director will provide medical and scientific input to preclinical and clinical stage assets focused on immunology / rheumatology / inflammatory...

• demonstrates medical leadership by contributing to key medical and scientific events, advisory boards, and rwe generation... • relevant therapeutic and clinical...

• proactively collaborates with the site & study operations (sso) clinical project managers (cpm) and cra managers as well as medical science liaisons, clinical...

Prior experience in medical affairs, with a focus on field medical roles... practical knowledge of clinician-facing medical affairs functions...

Provides matrix management of functional area representatives to cross functional clinical study teams... the associate director study leader, early oncology clinical...

Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates... lead the preparation of country specific agreements, confidentiality...

• oversee the clinical trial insurance process; track approvals, revisions and renewals of certificates... • lead the preparation of country specific agreements...

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...

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...

Participate in internal/external clinical evaluations, validation and verification... ensure successful implementation of all products at clinical sites...