Aurion Biotech→
Clinical Operations Intern, Documentation & Process Improvement
InternshipHybrid
Location
Boston, Massachusetts or Dallas/Fort Worth, Texas Candidates Only
Salary
$46k–$52k/yr
Experience
Not specified
Posted
3 weeks ago
Skills
microsoft officeclinical trial terminologyclinical practice (gcp)clinical researchbiotechnologypharmaceutical developmentcultural agilitypassion for science
Job Description
Summary: Aurion Biotech is a clinical-stage biotechnology company dedicated to restoring vision to millions of patients through innovative regenerative therapies. They are seeking a motivated and detail-oriented Summer Intern to support their Clinical Operations team, providing hands-on exposure to the operational execution of clinical trials and assisting with clinical trial documentation and study tracking.
Responsibilities:
- Create company specific templates and template language for technical documentation such as protocol template, ICF template, site operations manuals, etc. to streamline documentation processes going forward
- Supporting operational excellence projects, including quality reviews of Trial Master File (TMF) across all programs, tracking, and analysis of monitoring metrics
- Participate in internal Clinical Operations and cross-functional meetings; assist with agenda preparation, note-taking, and follow-up on action items
- Help maintain and organize study files, trackers, and shared workspaces (e.g., SharePoint or internal systems)
- Support quality and inspection-readiness activities by ensuring documentation is complete and filed appropriately under supervision
- Conduct data checks, reconciliations, or administrative reviews as assigned by Clinical Operations leadership
- Performs other duties as assigned
Required Qualifications:
- Currently enrolled junior (will begin senior year in fall 2026) in an undergraduate degree program in life sciences, public health, nursing, biomedical sciences, or a related field
- Strong organizational skills with attention to detail
- Ability to manage multiple tasks and meet deadlines in a fast-paced environment
- Proficiency with Microsoft Office (Word, Excel, PowerPoint); comfort working in shared document systems
- Interest in clinical research, biotechnology, or pharmaceutical development
- Strong interpersonal and communication skills, both written and verbal
- Ability to work effectively in a team environment and across global teams and vendors
- Excellent written, verbal, and interpersonal communication skills; ability to communicate with impact across diverse internal and external stakeholders
- Demonstrated cultural agility, integrity, and a passion for advancing transformative science
- A strong alignment with, and commitment to, Aurion Biotech's mission, vision, and core values
Preferred Qualifications:
- Familiarity with clinical trial terminology or GCP concepts preferred (coursework acceptable; not required)
Required Skills: Microsoft Office, Clinical trial terminology, Clinical Practice (GCP), Clinical research, Biotechnology, Pharmaceutical development, Cultural agility, Passion for science
Benefits: Full health insurance to full-time employees and their families, 401(k) matching, EAP, FSA, Generous PTO, Paid parking, Subsidized commuter passes, In-office catered lunches, Team events, Community projects
Benefits
Full health insurance to full-time employees and their families
401(k) matching
EAP
FSA
Generous PTO
Paid parking
Subsidized commuter passes
In-office catered lunches
Team events
Community projects