Intern - Clinical Research (Hybrid/Lexington, MA)

Partner Therapeutics • Lexington, MA

11h • $20 • Hybrid

About The Position

Partner Therapeutics (PTx) is a commercial biopharmaceutical company committed to improving the lives of patients with cancer and other serious diseases. Our dedicated team brings a rigorous approach to science, establishes deep partnerships with medical and scientific communities, and works tirelessly to expand potential treatment options and address unmet medical needs.
POSITION SUMMARY
We are seeking a highly motivated Summer Intern to join our Clinical organization for an office‑based internship. This role is ideal for students interested in drug development, clinical trial execution, and the integration of scientific insights into clinical strategy. The intern will collaborate closely with Clinical Development, Clinical Operations, and Translational Science teams to support ongoing clinical programs and cross‑functional initiatives. During the internship you will gain:
Hands-on exposure to the operational and strategic aspects of clinical research
Insight into how clinical trials are designed, executed, and analyzed
Experience working with multidisciplinary teams across Clinical Development, Clinical Operations, and Translational Science
Mentorship from industry experts and the opportunity to develop professional skills relevant to careers in biotech and pharma
The internship is structured as a hybrid role, with a minimum requirement of two on‑site days per week at our Lexington office to support collaboration with clinical and cross‑functional teams. This intern ship is funded through MassBio, therefore, to be eligible for this internship, you must be enrolled in a four-year accredited college in the state of Massachusetts, or you must be a resident of Massachusetts, enrolled in a college in or out of state.

Requirements

• Strong interest in clinical research, drug development, and the biopharmaceutical industry.
• Excellent organizational skills with high attention to detail.
• Strong written and verbal communication abilities.
• Ability to work collaboratively in a cross-functional, fast‑paced environment as well as independently.
• Proficient with Microsoft Office applications (Word, Excel, PowerPoint); experience with project tracking tools is a plus.
• Fluent command of spoken and written English.
• Currently pursuing a Bachelor’s or Master’s degree in Life Sciences, Public Health, Biomedical Engineering, Neuroscience, Pharmacy, or a related field, with at least two years of undergraduate coursework completed.

Nice To Haves

• Knowledge of HIPAA and ICH GCP and regulations regarding clinical research.
• At least three years of undergraduate coursework completed.

Responsibilities

• Assist Clinical Development teams in preparing and reviewing study-related documents, including clinical study data, clinical study reports, and meeting materials.
• Support Clinical Operations with tracking study activities, organizing trial master file documentation, and maintaining operational dashboards or trackers.
• Translational Scientists with data summaries, literature reviews, and preparation of materials that integrate biomarker and clinical insights.
• Participate in cross-functional team meetings and support follow-up actions, including note-taking, summarizing key decisions, and documenting next steps.
• Contribute to competitive intelligence research and landscape assessments to support strategic clinical planning.
• Present a capstone project at the end of the internship summarizing key learnings and contributions.

What This Job Offers

• Career Level: Intern