Clinical Trial Coordinator

Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global...

According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. - Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. - Ensures allocated tasks are performed on time, within budget and to a...

**Clinical Trial Coordinator (CTC Shipment)** Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The Clinical Trial Coordinator, CTC Shipment, supports clinical supply & non-clinical supply management and ensures...

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...

Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system. Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads. Supports the maintenance of study specific documentation and systems including but not...

**Job Description**: Under the oversight of the line-manager, this role is responsible for comprehensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

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...

**Responsibilities**: - Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist (iCRS), Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines. -...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

**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...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

Clinical supply and Non-clinical supply management (mainly focus on import and export activities), in collaboration with other country roles. Update clinical trial databases, report and trackers as required. Ensure collaboration and distribution of study tools and documents. Prepare documents and correspondence. Collate, distribute/ship, and archive clinical...

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...

**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...

Excellent technical/IT skills. Able to understand the impact of technology on studies and to use and develop computer skills while making appropriate use of systems/software. Knowledge of relevant operational procedures, systems and quality guidelines regarding clinical studies. Able to work independently as well as in a team. Professional attitude with good...

This position is responsible for project management of the assigned studies, accountable for performance for assigned protocols, leads local study teams to high performance on trains in the protocol other local roles, closely collaborates with and supports CRAs as protocol expert etc. **WHAT YOU WILL DO** **Key Responsibilities**: - Main Point of Contact...

Main Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT). **Responsible for project management of the assigned studies**: pro-actively plans, drives and tracks execution and performance of deliverables/timelines/results to meet country commitments from feasibility and site selection, recruitment,...

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...