Non-Clinical Development Intern
About The Position
Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential. Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you’re ready to join us at the edge of something unstoppable, let’s make a profound impact together for our patients, for your career, for what’s beyond. You can view our latest corporate deck and other presentations here. As the Non-Clinical Development Intern reporting to the Vice-President, Pre-Clinical Pharmacology and Toxicology, you will obtain hands-on experience within a biotechnology environment working alongside our Non-Clinical Development team. This role provides hands on learning on how drugs are developed and how nonclinical studies are designed, conducted, and managed across DMPK, Pharmacology, and Toxicology disciplines to support discovery and development. This position is a 10-week paid summer internship $22/hour working 40 hours a week onsite at our San Francisco facility. The internship dates are June 8 through August 14. Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. Your work will primarily encompass: Supporting the design and protocol development of nonclinical studies Assisting with data and report review Assisting with outsourcing activities and coordination with Contract Research Organizations (CROs) Participating in study management activities, including remote monitoring and tracking timelines and deliverables Summarizing and presenting findings in group meetings Collaborating with cross-functional teams including Medicinal Chemistry and Discovery Biology You will also: Learn the scientific and regulatory rationale for nonclinical studies in oncology drug development Understand how nonclinical studies support clinical development Gain exposure to outsourced and virtual study execution models Build a foundation to further your career development in DMPK, Pharmacology, and Toxicology research and its application to drug discovery and development Ideal Candidate Profile >>> Highly Motivated Student Studying Biology, Pharmacology, Toxicology, or Related Field. A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role.
Requirements
- Currently enrolled in a 4-year undergraduate program or 2026 graduate, required
- Currently a standing junior or senior, required
- Currently majoring in Biology, Pharmacology, Toxicology, Pharmaceutical Sciences, or closely related field of study, required
- Organized and detail-oriented
- Highly self-motivated with a strong desire to learn
- Passion for science
Nice To Haves
- Coursework in pharmacology, toxicology, or related disciplines prior to internship, preferred
- Previous research or internship experience in a scientific setting, preferred
Responsibilities
- Supporting the design and protocol development of nonclinical studies
- Assisting with data and report review
- Assisting with outsourcing activities and coordination with Contract Research Organizations (CROs)
- Participating in study management activities, including remote monitoring and tracking timelines and deliverables
- Summarizing and presenting findings in group meetings
- Collaborating with cross-functional teams including Medicinal Chemistry and Discovery Biology
- Learn the scientific and regulatory rationale for nonclinical studies in oncology drug development
- Understand how nonclinical studies support clinical development
- Gain exposure to outsourced and virtual study execution models
- Build a foundation to further your career development in DMPK, Pharmacology, and Toxicology research and its application to drug discovery and development
Benefits
- We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers.
- A Summary of Benefits is available for all applicants.
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What This Job Offers
Job Type
Full-time
Career Level
Intern
Number of Employees
11-50 employees
