Clinical Trials Associate – Global CRO (US/Canada)

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

Job summary

Worldwide Clinical Trials is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are performed timely and accurately.

You will arrange and track system access, maintain document quality on project portals, assist with preparation and shipment of regulatory materials, and maintain the trial master file. Strong English, attention to detail, and MS Office proficiency are essential.

Qualifications

• Degree level qualification or equivalent experience.
• Minimum of one year’s experience in a related role.
• Excellent written and verbal English.
• Proficient in MS Office applications (Outlook, Word, Excel and PowerPoint).

Responsibilities

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

Skills

MS Office

Attention to detail

Organizational skills

English proficiency

Multitasking

Education

Degree or equivalent experience

Job description

Worldwide Clinical Trials is seeking a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are performed timely and accurately.

You will arrange and track system access, maintain document quality on project portals, assist with preparation and shipment of regulatory materials, and maintain the trial master file. Strong English, attention to detail, and MS Office proficiency are essential.