Clinical Trial Coordinator

Not Interested
Bookmark
Report This Job

profile Job Location:

Taipei City - Taiwan

profile Monthly Salary: Not Disclosed
Posted on: 6 days ago
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

About the Role

Join Thermo Fisher Scientific Inc. where you will become part of an experienced and hardworking team in Taiwan! As part of a world-class organization you will work to ensure the flawless execution of clinical studies and contribute to groundbreaking scientific advancements. This is an outstanding opportunity to collaborate with dedicated professionals and achieve ambitious goals together.

Key Responsibilities

  • Maintain up-to-date participating centers information including all contact details.
  • Prepare Investigator and Sponsor files (electronic and/or paper) with essential documents for the initiation of sites participating in clinical studies.
  • Provide administrative assistance for the preparation gathering review monitoring and filing of all documentation needed for regulatory and/or ethics committee submissions.
  • Support the execution of Confidentiality Agreements Conflict of Interest forms and Data Privacy Notices.
  • Assist with the management of investigator site payments preparation of purchase orders and task orders for services.
  • Coordinate vendor management manage local study materials and ensure the accurate distribution tracking storage and reconciliation of clinical and ancillary supplies.
  • Develop and maintain accurate tracking information related to site and supplier contracts and external costs.
  • Ensure the accuracy of relevant study systems and set up new employees and site staff on relevant systems.
  • Plan and prepare logistics for monthly reports local Investigator meetings and other study-related activities.
  • Engage in local study meetings and support GSK study staff with study-related activities such as coordinating meetings scheduling travel producing minutes and maintaining study documentation.

Qualifications

  • Demonstrated experience providing administrative assistance for clinical studies.
  • Strong organizational skills with a keen attention to detail.
  • Ability to prioritize effectively and communicate with medical staff physicians and scientists.
  • Knowledge of ICH GCP GSK written standards and willingness to continuously learn and adapt to evolving systems and technologies.

Why Thermo Fisher Scientific

Our Mission drives us to help customers create a healthier cleaner and safer world. Joining our team means collaborating with diverse colleagues who share values and dedication to accelerating research. You will address complex scientific challenges and promote technological innovation. This is your chance to define a significant impact and join something outstanding!


Required Experience:

IC

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAbout the RoleJoin Thermo Fisher Scientific Inc. where you will become part of an experienced and hardworking team in Taiwan! As part of a world-class organization you will work to ensure the flawless execution of clinical s...
View more view more

Key Skills

  • CSS
  • Cloud Computing
  • Health Education
  • Actuary
  • Building Electrician

About Company

Company Logo

Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

View Profile View Profile