Impress employers and recruiters.
Choose from hundreds of resume examples.

Impress employers and recruiters.
Choose from hundreds of resume examples.

Target Resume Now

About the Role

The Clinical Research Associate Intern will assist the Clinical Monitoring team in various study related activities across all active platform trials being conducted at QLHC. This position requires the ability to be detailed-oriented, organized, and productive with a keen interest in clinical research space.

Responsibilities

• Assist with reconciliation of lab specimens and corresponding CRFs.
• Assist with regulatory document collection, reconciliation and filing into the TMF.
• Assist with updates of site contact and distribution lists across the assigned portfolio.
• Complete projects and tasks consistent with department objectives.
• Collaborate with cross-functional teams on assigned projects.
• Perform other duties as assigned.
• Contribute to the company culture of being collaborative, respectful, transparent, ethical, efficient, and high-achieving.

Requirements

• General knowledge of oncology or willingness to undergo rigorous and fast learning independently.
• Excellent time management skills.
• Ability to exercise critical thinking skills in selecting methods, techniques, and evaluation criteria.
• Proficient in Microsoft Word, Excel, and Access and the ability to quickly learn other software tools and applications.

Skills

• Detailed-oriented
• Organized
• Productive
• Microsoft Word
• Microsoft Excel
• Microsoft Access

Education Level

• Bachelor of Science degree or candidate for future degree preferably in natural sciences or related field, or related practical experience.