Overview

• Salary

  60,000 THB ~ 120,000 THB

• Industry

  Medical

• Job Description

  【Job Summary】
  - Responsible for setting up, coordinating and supervising clinical studies (trials) with medicines, medical nutrition or medical devices
  - Develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials.
  
  【Responsibilities】
  - Creating and writing trial protocols, and presenting these to the steering committee.
  - Identifying, evaluating, and establishing trial sites, and closing sites down on completion of the trial.
  - Training site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
  - Liaise with the ethics committee regarding the rights, safety, and well-being of trial subjects.
  - Ordering, tracking, and managing IP and trial materials.
  - Overseeing and documenting IP dispensing inventory, and reconciliation.
  - Protecting subjects’ confidentiality, updating their information, and verifying IP have been dispensed and administered according to protocol.
  - Conducting regular site visits, coordinating project meetings, and writing visit reports.
  - Implementing action plans for sites not meeting expectations.
  - Liaising with regulatory authorities.
  - Ensuring compliance with SOPs and local regulations, and ICH and GCP guidelines.
  - Other tasks and responsibilities as needed.