Intern, Clinical Pharmacology

Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers.

Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission.

Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust.

By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.

Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients.

Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients.

It’s our work, our passion, and our legacy.

We invite you to join us.  

Hybrid

Employee Value Proposition:

This internship offers a unique opportunity for a motivated college student to gain hands-on experience in clinical pharmacology by contributing to clinical/translational research projects within a dynamic and collaborative environment.

We are committed to providing a valuable learning experience and mentorship to support the intern's professional development and growth.

Position Summary:

We are seeking a motivated and enthusiastic college student to join our Clinical Pharmacology team as an intern.

This internship offers valuable hands-on experience in the field of pharmaceutical research and development, specifically focusing on clinical pharmacology.

The intern will work closely with our team of professionals to support various aspects of clinical pharmacology including clinical/translational research projects.

Performance Objectives:


* Participate in literature review and research to support clinical/translational research projects.


* Collect, organize, and analyze pharmacokinetic (PK) and pharmacodynamic (PD) data from clinical trials.


* Apply critical thinking to integrate what has been published in the literature with PK and PD data from clinical trials to provide study team with dose optimization guidance.


* Contribute to the preparation of presentations and scientific publications.


* Attend team meetings, training sessions, and other departmental activities as required.


* Adhere to all relevant regulatory guidelines, protocols, and standard operating procedures (SOPs) to ensure compliance with industry standards.

Education/Certification Requirements:   


* Currently enrolled in a Bachelor's or Master's degree program in a relevant scientific field (e.g., pharmacology, pharmacy, biochemistry, biology, or related discipline).

Knowledge, Skills, and Abilities:


* Strong academic background with coursework in pharmacology, pharmacokinetics (PK), bioch...