Lab Operations Associate Scientist: Trial Master File & Data

IQVIA; North Carolina; On-site; USD 43,000 - 89,000; Full time

Job summary

IQVIA Laboratories in Durham, NC seeks an Associate Scientist, Laboratory Operations to perform routine laboratory analysis and support documentation and study file delivery. The role collaborates with clinical and regulatory teams to ensure compliant study execution.

Ideal candidates have 3-4 years of administrative support experience and at least 1 year of clinical research experience, with proficiency in Word, Excel and PowerPoint.

Qualifications

• High School Diploma or equivalent required.
• 3-4 years administrative support experience.
• Minimum one year clinical research experience strongly preferred.
• Computer skills including Word, Excel and PowerPoint.
• Knowledge of Good Clinical Practice and ICH guidelines.
• Knowledge of applicable protocol requirements.
• Experience with Trial Master File maintenance and clinical documentation.

Responsibilities

• Perform routine laboratory analysis and testing procedures and document results.
• Support clinical and regulatory teams with documentation and study file maintenance.
• Update and maintain clinical documents and systems, including the Trial Master File.
• Assist with preparation, handling, distribution, filing, and archiving of clinical docs and reports.
• Coordinate tracking of Case Report Forms and clinical data flow.
• Serve as central contact for project communications and documentation.
• Maintain inventory, equipment logs, data compilation, and scheduling support.

Skills

Written and verbal communication

Time management

Organizational skills

Teamwork

Attention to detail

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Education

High School Diploma or equivalent

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

IQVIA Laboratories in Durham, NC seeks an Associate Scientist, Laboratory Operations to perform routine laboratory analysis and support documentation and study file delivery. The role collaborates with clinical and regulatory teams to ensure compliant study execution.

Ideal candidates have 3-4 years of administrative support experience and at least 1 year of clinical research experience, with proficiency in Word, Excel and PowerPoint.