INTERNSHIP DETAILS

Intern- Clinical Research Assistant

CompanyQuantum Leap Healthcare
LocationSan Francisco
Work ModeOn Site
PostedJuly 29, 2026
Internship Information
Core Responsibilities
The intern will assist the clinical monitoring team with lab specimen reconciliation, regulatory document filing, and site contact list updates. They will also collaborate with cross-functional teams to support various platform trials.
Internship Type
full time
Company Size
Not specified
Visa Sponsorship
No
Language
English
Working Hours
40 hours
Apply Now →

You'll be redirected to
the company's application page

About The Company

No description available for this Company.

About the Role


SUMMARY AND DETAILS OF POSITION


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.


Principal Responsibilities


  • Assist with reconciliation of lab specimens and corresponding CRFs.
  • Assists with regulatory document collection, reconciliation and filing into the TMF.
  • Assists 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.


Required Education and Experience


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


Disclaimer: This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.


Key Skills
Clinical ResearchRegulatory Document CollectionLab Specimen ReconciliationTime ManagementCritical ThinkingMicrosoft WordMicrosoft ExcelMicrosoft AccessData ReconciliationTMF FilingOncology Knowledge
Categories
Science & ResearchHealthcareAdministrative