Clinical Trials Assistant 1

**Overview**: **Role: Clinical Trial Manager** **Location: Thailand, home-based** As a Clinical Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. - You will be partnering with one of the world’s premier Biopharmaceutical companies. Working across a vast...

Track (e.g. essential documents) and report (e.g. Safety Reports). Update clinical trial databases (CTMS) and trackers. Ensure collation and distribution of study tools and documents. Clinical supply & non-clinical supply management, in collaboration with other country roles. Manage Labeling requirements and coordinate/sign translation change request, in...

**Trial and site administration**: - Clinical supply & non-clinical supply management (mainly focus on import and export), in collaboration with other country roles. - Update clinical trial databases, report and trackers as required - Ensure collation and distribution of study tools aFnd documents. **Document management**: - Prepare documents and...

The Clinical Trial Educator (CTE) group is looking to appoint a **Clinical Trial Educator **in** IQVIA Thailand**. As our specialist CTE, you will be able to accelerate patient enrollment, improve site performance and help streamline studies in ways no other team member can. You’ll often be your sites’ go-to person for information, advice and problem...

IQVIA Thailand is currently looking to hire a motivated, creative, and enthusiastic clinical trials professional to join our team as a Clinical Trials Educator (CTE) on a 12-months fixed term contract. As our specialist CTE, you will be able to accelerate patient enrolment, improve site performance and help streamline studies in ways no other team member...

**About the Department** Novo Nordisk is a global healthcare company with more than 95 years of innovation and leadership in diabetes care. This heritage has given us experience and capabilities that also enable us to help people defeat obesity, haemophilia, growth disorders and other serious chronic diseases. Headquartered in Denmark, Novo Nordisk employs...

**Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. **Essential Functions** - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in...

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol and...

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol and...

**THE OPPORTUNITY** The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, Merck policies and procedures, quality standards and adverse event reporting requirements internally and...