[Hiring] Clinical Trial Administrator @Fortrea

Role Description

The Clinical Trial Administrator (CTA) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the CTA shall reflect their experience and level of contribution which they can make to the project. The CTA performs study-related tasks as required by the department, including:

• Communicate with project team members regarding study updates.
• Maintain documentation as required by protocols, SOPs, and regulatory standards to ensure timely production of high-quality clinical data.
• Provide systems support and track information related to the status of study activities.
• Assist with general administrative functions as required.

Activities will be conducted in compliance with Company or Sponsor SOPs and regulatory standards and guidelines applicable.

Qualifications

• Diploma – Associate degree or equivalent.
• In lieu of the above requirement, candidates with 1-2 or more years of relevant Clinical Research experience in pharmaceutical or CRO industries may be considered.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• Speaking English and local language.
• Writing/Reading English and local language.

Requirements

• Minimum one (1) year administrative experience or equivalent training.
• Good oral and written communication skills.
• Good organizational and time management skills.
• Computer literacy (Microsoft Office Suite: Word, Excel, PowerPoint).
• Aptitude for handling and proof-reading numerical data, some spreadsheet software competency.
• Good typing skills.
• Good spelling and proof-reading skills.
• Ability to operate standard office equipment (e.g., fax, copier).
• Works efficiently and effectively in a matrix environment.

Benefits

• General Office Environment or Home-based.
• Travel Requirements: 0-20% (Local, Domestic, Regional, Global).