Intern, Clinical Data Management and Biostatistics

About The Role

Jumpstart your career in clinical research with this hands-on Data Management and Biostatistics internship! You’ll dive into the full clinical data lifecycle, from data collection to database lock, working side-by-side with experienced Clinical Data Management and Biostatistics teams. Gain real-world experience with industry-leading tools like Veeva EDC, CDB workflows, and JReview, and see how high-quality data drives critical decisions.

This is your chance to build practical skills, make a tangible impact, and prepare for a successful career in Clinical Data Management or Biostatistics. Let’s talk about some of the key responsibilities of the role: Gain hands-on experience in clinical data management, reviewing clinical trial data in Veeva EDC and tracking issues in CDB Perform data checks, listing reviews, and reconcile external data to identify trends, inconsistencies, and outliers Support biostatistics activities by reviewing tables, listings, and figures, and exploring data for insights Work with industry-leading tools and systems, including Veeva EDC, CDB, JReview, Microsoft Excel, SAS or R, and gain introductory exposure to CDISC standards (SDTM/ADaM) Work closely with the Clinical Development and Clinical Operations teams through active participation in data review meetings, and project discussions Build practical, real-world skills that prepare you for a career in Clinical Data Management or Biostatistics Factors for Success: Current enrolment in an undergraduate or graduate program majoring in Biostatistics, Statistics, Data Science, Epidemiology, Public Health, or a related field Strong attention to detail and interest in clinical data quality Basic understanding of statistics and data analysis concepts Proficiency in Microsoft Excel Strong organizational, written, and verbal communication skills Ability to work independently and collaboratively in a team environment Familiarity with clinical research, healthcare data, and Good Clinical Practice (GCP) Prior exposure to Veeva EDC, JReview, or clinical data review tools preferred but not required Basic knowledge of CDISC standards (SDTM/ADaM) preferred but not required A Few Other Details Worth Mentioning: The position will be based in our beautiful Irvine office, complete with a courtyard, table tennis, snacks and drinks, and occasional catered meals.

We provide a hybrid work environment. We are passionate about our culture! Our Tarsans live our values of commitment to patients, empowerment to champion innovation, and teamwork to amplify impact. Your ten-week summer internship at Tarsus will consist of a variety of activities to enhance your experience such as lunch and learns, development opportunities, offsite volunteering, company-wide social events, and more!

This position reports directly to our Assoc Dir, Clinical Data Mgmt The expected hourly pay for this position is $26/hour for an undergraduate student and $45/hr for a graduate student. #LI-HybridTarsus Pharmaceuticals, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Tarsus Pharmaceuticals is a biopharmaceutical company specializing in developing novel treatments for patients with rare and serious inflammatory eye diseases. The company is dedicated to advancing innovative therapies that address significant unmet medical needs in ophthalmology.