Remote Clinical Data Entry Intern — Research Support

Sarah Cannon Research Institute; United States; Remote; USD 16,740 - 20,088; Part time

Job summary

Sarah Cannon Research Institute is seeking an intern for a remote, US-based position, approximately 8 weeks starting mid-July. Relocation assistance and visa sponsorship are not available.

In this role, you’ll help ensure the accuracy and integrity of critical research data—an essential part of bringing new therapies to life. You’ll enter and update data, review for completeness, organize and digitize records, support QC processes, generate basic reports, and collaborate with cross-functional

Qualifications

• Pursuing or recently completed degree in life sciences, health administration, business, or related field.
• Strong attention to detail and commitment to high-quality work.
• Basic proficiency in Excel, Google Sheets, or similar tools.
• Strong organizational skills and ability to manage multiple tasks.
• Interest in clinical research, healthcare, or data management.
• Clear communication and collaborative mindset.

Responsibilities

• Enter and update clinical and operational data in internal systems and databases.
• Review data for completeness, accuracy, and consistency; identify and resolve discrepancies.
• Organize, maintain, and digitize research documentation and records.
• Support data validation and quality control processes in line with protocols.
• Generate basic reports or summaries to support team insights and decision-making.
• Maintain confidentiality of patient, clinical, and proprietary information.
• Collaborate with cross-functional teams, including clinical and administrative staff, to ensure data integrity.
• Other duties as assigned.

Skills

Detail-oriented

Collaboration

Communication

Education

Life Sciences

Health Administration

Business

Tools

Excel

Google Sheets

Job description

Sarah Cannon Research Institute is seeking an intern for a remote, US-based position, approximately 8 weeks starting mid-July. Relocation assistance and visa sponsorship are not available.

In this role, you’ll help ensure the accuracy and integrity of critical research data—an essential part of bringing new therapies to life. You’ll enter and update data, review for completeness, organize and digitize records, support QC processes, generate basic reports, and collaborate with cross-functional