Job Description
Job Description
Internship Session
Summer 2025
Term/duration
College Level/New Grad
- 10 weeks
Start Date
June 9, 2025
End Date
August 15, 2025
Title
Clinical Research Intern
Department
Clinical Research
Reporting Line
Senior Director, Clinical Research
Location
- On-site Program, Scottsdale, Arizona - Headquarters
- Remote from home may be considered after 5 weeks
Application
Apply via online application posting
Education
College Level/New Grad:
- Must be actively enrolled and in good standing with their program
Condition
- Paid internship
- Internship for school credit
- Both (evaluated on a per applicant basis)
Compensation
- Minimum wage of the applicable work state
Benefits
If during an internship, work-related travel is necessary:
- CND reimbursed travel expenses
- Per diem meal stipend
Required Training
Upon their start date, all interns will be required to complete the following training:
- New Hire Security Training
- Semi-Annual Cyber Training
Any interns with access to patient health information will also be required to complete the following training:
- Steri-Safe: Annual HIPAA Staff Training
- Steri-Safe: Advanced HIPAA
Optional Training
Additional training for Clinical Research may include the following, to be completed by the intern on their own time:
- NIDA GCP and CFR
- CITI GCP, Biomedical Research, Responsible Conduct of Research
- NIH OCRECO Intro to the Principles and Practice of Clinical Research
Process
- Online application submitted followed by an interview.
- CND background check to include drug screen for all accepted applicants.
- Completion of CND onboarding documents
Overview
CND Life Sciences is seeking a motivated and detail-oriented intern to join our Clinical Research team. This internship provides hands-on experience in the life sciences industry and is well-suited for students pursuing degrees in life sciences, public health, medicine, or related fields. As a Clinical Research Intern, you will support key initiatives including data entry, data cleaning, data analysis, literature reviews and background research to inform the design, planning and execution of research projects. You will also collaborate with internal stakeholders to assist and support clinical trials. Additional duties may be assigned as seen fit for the growth of the candidate and needs of the project(s).
In this role, you will gain:
- Exposure to cross-functional collaboration and strategy development
- Opportunities to contribute to meaningful patient-centered clinical research projects
- Mentorship from experienced professionals in Clinical Research and related fields
Ideal Candidate Qualifications:
- Strong written and verbal communication skills
- Excellent organizational skills and attention to detail
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook)
- Experience with data entry platforms is a plus
- Ability to work both independently and collaboratively in an on-site, remote or hybrid environment
This is a great opportunity to build foundational experience in a mission-driven, fast-paced life sciences company making an impact in patient care and clinical research.