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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates strong capabilities in clinical research support, data quality assurance, and effective communication within cross-functional teams. Proficient in preparing presentations and literature reviews relevant to oncology compounds and clinical trials.
Highest-signal resume keywords
Clinical Research ExperienceData Quality AssuranceMicrosoft Office ProficiencyOncology KnowledgeCross-Functional Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchData ReviewLiterature ReviewStudy-Progress TrackingClinical Trial ProcessesRegulatory DocumentationOncology TreatmentsTrial Methodologies
Soft Skills
Excellent Written CommunicationExcellent Verbal CommunicationIndependent WorkCollaborative Teamwork
Tools & Technologies
Microsoft WordMicrosoft PowerPointMicrosoft Excel
Industry Keywords
Pharmaceutical IndustryBiotechnology IndustryClinical PharmacyAccredited CollegeMBAMaster'sPharmDPh.D.
About the role
Key responsibilities & impact- Support clinical development of oncology compounds and assist with day-to-day execution of clinical trials, focusing on data quality
- Participate in cross-functional discussions with clinical, statistics, operations, and data management teams
- Prepare literature reviews, slide decks, and study-progress tracking documents
- Perform data review and identify clinical findings to maintain study data quality
- Conduct background research on oncology disease states, treatments, and trial methodologies
- Assist in preparing internal presentations and literature summaries
- Learn about the clinical scientist role through meetings, mentorship, and guided projects
Requirements
What you’ll need- Must be available to work a full-time schedule
- Expected continued enrollment in an accredited college or university following the internship program / co-op
- Student must be located in the United States for the duration of the internship program
- 18 years or older
- Graduated with a bachelor’s degree from an accredited college or university
- Currently enrolled in an MBA, Master’s, PharmD, or Ph.D. program from an accredited college or university
- Completion of the first year of the applicable MBA, Master’s, PharmD, or Ph.D. program before the internship starts
- Preferred degree concentration: Pharmacy
- Excellent written and verbal communication skills
- Ability to work independently and collaboratively within cross-functional teams
- Proficiency in Microsoft Office (Word, PowerPoint, Excel)
- Prior experience in clinical research (coursework, clerkships, projects) and/or clinical pharmacy
- Familiarity with clinical trial processes or regulatory documentation
- Strong interest in pursuing a career in the pharmaceutical or biotechnology industry
- Candidates must be authorized to work in the U.S. for the duration of this program
Benefits
Comp & perks- Competitive benefits
- Collaborative culture
- Professional and personal growth and well-being support
- Executive and social networking events
- Community volunteer projects
- Inclusive culture valuing diversity of thought and experience
- Reasonable accommodation for individuals with disabilities