Why study Molecular, Cellular and Biochemical Pharmacology : Applied Pharmacology & Drug Toxicology?

Master's in Pharmacology students gain an educational foundation in Pharmacology plus a behind-the-scenes look into the FDA drug approval process including nonclinical & clinical safety assessments and regulatory guidance. MS students also have the unique advantage to network with experts currently working in the field through special lectures and networking events. Graduates of our program are prepared for employment in the biopharmaceutical and biotech industries, contract research organizations (CROs), government (FDA), or continuing education in medical (MD/DO) or graduate (Ph.D.) school.

Admission Requirements

  • Undergraduate degree in life sciences or a STEM discipline (GPA 3.0 or higher)
  • Unofficial Transcript(s)
  • Submission of proof of English language proficiency for non-native English speakers (For those submitting a TOEFL score, a minimum 90 iBT or equivalent is required)
  • Reference letters (minimum 2)

Women and underrepresented minority students are encouraged to apply. Scholarship opportunities are available for underrepresented students.  

Previous biomedical research experience is helpful but not required for admission.

Due to the diversity of our students’ interests, our program works diligently to introduce them to new experiences in drug safety while providing a solid foundation in pharmacology. About half of our students use our program as a gap year experience, preparing for advanced academic training in the life sciences (MD, PhD, DMD, PharmD, DVM), with our remaining graduates employed in academia or with contract research organizations associated with the pharmaceutical industry.

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The MS in Pharmacology program provides students with a special emphasis in nonclinical drug development. This research area applies pharmacologic and toxicologic principles to investigate new chemical and biological therapies for safety before they are administered to humans. It is a necessary component of the FDA drug approval process, which aims to evaluate a new drug’s capacity to cause adverse effects at therapeutic doses (Safety Pharmacology) and/or harm at high doses (Drug Toxicology). These two equal, but distinct, aims (Safety Pharmacology and Drug Toxicology) are vital for protecting the public against harmful new drugs. 

Explore unique opportunities, faculty, and resources available in Pharmacology and Systems Physiology

The University of Cincinnati and all regional campuses are accredited by the Higher Learning Commission.

Contact Information

Dr. Katie Hobbing
231 Albert Sabin Way MSB 4203
Cincinnati, OH 45267-0576
(513) 558-4159
katie.hobbing@uc.edu

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Program Code: 26MAS-MCBP-MS-MCBP-SP