EMPREGO CLINICAL TRIAL MANAGER REGULATORY

clinical trial manager clinical trial managers are an integral part of clinical trial delivery, working alongside clinical teams to improve patients’ lives by bringing...

clinical trial manager clinical trial managers are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing...

We are looking for a clinical trial leader (ctl) to join our a-team (office*/remote)... requests appropriate clinical operations staffing, workload and resources...

Develop annual regulatory budget for philippines filings/variations/registrations/license renewals and department needs... strong ability to assimilate information...

• awareness of applicable clinical research regulatory requirements, i... essential functions • assist clinical research associates (cras) and regulatory and start-up...

Local trial manager – sponsor dedicated... clinical project management services provide local management of a clinical trial (s) in a country level...

Local trial manager - sponsor dedicated... clinical project management services provide local management of a clinical trial (s) in a country level...

Possess basic knowledge of global/regional/national country requirements and regulatory affairs procedures for clinical trial authorization, licensing, and lifecycle...

Involvement in processes that influence clinical trial operational performance... …our commitment to diversity in clinical trials, clinical research, and advancing...

Day to day responsibilities will include: verifying and/or correcting research study information on source documents; researching queries and variances; providing...

Accurate input of trial data into the electronic data capture (edc) system and tracking visits and procedures completed against budget in the clinical trial management...

#li-nrj #li-onsite iqvia is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare...

At least 3 years relevant experience in a scientific or clinical environment... in-depth knowledge of clinical systems, procedures, and corporate standards strong...

• 1-3 years clinical research experience working in the site activation / regulatory and start up department in brazil... • prepare site regulatory documents, reviewing...

You will ensure adherence to good clinical practices (gcp), evolving regulatory requirements, and company working procedures... ensuring all trial essential documents...