Clinical Trials Associate: Impactful Study Coordination

Worldwide Clinical Trials Holdings, Inc.; North Carolina; Hybrid; USD 23,000 - 46,000; Full time

Job summary

Worldwide Clinical Trials, a global midsize CRO, is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects are performed timely and accurately.

You will arrange system access for project team members, maintain project documentation on portals, assist with shipment of trial materials, and maintain QA logs with strong attention to detail and quality.

Qualifications

• Bachelor's degree or equivalent experience required.
• Minimum of one year's experience in a related role.
• Excellent written and verbal English; fluency in the local language.

Responsibilities

• Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.).
• Maintain and quality audit to ensure latest revisions of documents are on project portals.
• Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File.
• Maintain version and quality control of project documentation and submit to trial master file.
• Assist with tracking and maintenance of project-related information, including site medical QA logs.

Skills

MS Office proficiency

Attention to detail

Organizational skills

Problem solving

Multitasking

Education

Bachelor's degree or equivalent experience

Tools

MS Office Suite

Job description

Worldwide Clinical Trials, a global midsize CRO, is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects are performed timely and accurately.

You will arrange system access for project team members, maintain project documentation on portals, assist with shipment of trial materials, and maintain QA logs with strong attention to detail and quality.