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Clinical Research Data Entry Intern - Remote US

Sarah Cannon Research Institute

5h ago

0Data-entryTN, USjobspy_indeed
remoteindeed

Job Description

**It’s More Than a Career, It’s a Mission.** Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community\-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission\-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day. **Our Mission** People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting\-edge research, SCRI is redefining cancer care around the world. Our **Sarah Cannon Research Institute** is adding several detail\-oriented, curious, and motivated **Data Entry Interns** to our team for 8\-week internships this summer. This is a great opportunity to gain hands\-on experience in clinical research operations while contributing to work that ultimately impacts patient care. **The internships are remote, US\-based for approximately 8\-weeks beginning in 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. ### **What You’ll Do:** * Accurately enter and update clinical and operational data into internal systems and databases * Review data for completeness, accuracy, and consistency, identifying and resolving discrepancies * Assist with organizing, maintaining, and digitizing research documentation and records * Support data validation and quality control processes in compliance with research protocols * Generate basic reports or summaries to support team insights and decision\-making * Maintain strict 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 ### **What You Bring:** * Currently pursuing or recently completed a degree in Life Sciences, Health Administration, Business, or a related field * Strong attention to detail and a commitment to producing high\-quality, accurate work * Basic proficiency in Microsoft Excel, Google Sheets, or similar tools * Strong organizational skills and the ability to manage multiple tasks effectively * Interest in clinical research, healthcare, or data management * Clear communication skills and a collaborative mindset ### **Nice to Have:** * Previous experience in an administrative, research, or data entry role (academic or professional) * Familiarity with clinical research processes