EMPREGO CLINICAL TRIAL MANAGER REGULATORY

Req • knowledge of clinical trials - knowledge of clinical trial conduct in addition to skill in applying applicable clinical research regulatory requirements i...

As a clinical trial manager at icon, you will lead global clinical trials, interpret complex medical data, and contribute to the development of groundbreaking treatments...

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

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

Purpose: the clinical trial assistant supports the local trial manager (ltm) and/or site manager (sm) to ensure optimal management of all documents with logistical...

Regional clinical study senior manager - spanish is a plus... as required, supports planning and execution of the clinical study report in collaboration with global...

Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst...

Supports start-up team in regulatory submissions... may review and track of local regulatory documents... clinical trial coord - performs department, internal, country...

Directs development team strategy and deliverables overseeing the development strategy, clinical development plan and clinical protocols in india...

The senior, site manager will partner with the local trial manager (ltm), clinical trial assistant (cta) and tdl (trial delivery leader) to ensure overall site management...

Ecrts, iss, ise, bimo, p21 checks) and providing support for regulatory questions; lead and organize study level programming and oversight activities for analysis...

• input visit data into clinical trial management system (ctms) to track patient visits and procedures completed against the study budget...

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

Basic knowledge of clinical trials... accurate input of trial data into the electronic data capture (edc) system and tracking visits and procedures completed against...

• inform team members of completion of regulatory contractual... iqvia is a leading global provider of clinical research services, commercial insights and healthcare...

• inform team members of completion of regulatory contractual... anvisa (moh) - initial deec submission, substantial protocol amendments, faec update (anvisa clinical...