Labcorp is seeking a Clinical Trial Program Manager intern to contribute to product team initiatives that improve the use of protocol and lab documents during clinical trials. The internship will last 12 weeks, and the candidate will be immersed in hands-on work, gain valuable exposure to Labcorp's global business, culture, and leadership, and receive dedicated mentoring connections.
Requirements
- Currently enrolled in a graduate program (Master’s or Ph.D.) in Clinical Research, Public Health, Biomedical Sciences, Pharmacy, Nursing, or a related field.
- Coursework or training in clinical trial design, protocol development, or medical terminology preferred.
- Prior experience writing, reviewing, or interpreting clinical trial protocols (academic, industry, or internship experience acceptable).
- Familiarity with clinical trial lab manuals, including structure and common laboratory procedures.
- Working knowledge of clinical and medical terminology, with ability to translate lay terms into standardized codes using available resources (e.g., ICD10).
- Exposure to clinical data standards (e.g., CDISC, OMOP) or ontology concepts.
- Experience with data entry and documentation in clinical systems preferred.
- Interest or experience in AI/ML applications in clinical research (e.g., creating test cases, generating examples) is desirable.
Benefits
- Medical
- Dental
- Vision
- Life
- STD/LTD
- 401(k)
- Paid Time Off (PTO) or Flexible Time Off (FTO)
- Tuition Reimbursement
- Employee Stock Purchase Plan
