Clinical Trial Management Post Master's Certificate Postgraduate Programme By Temple University |TopUniversities
Subject Ranking

# 351-400QS Subject Rankings

Main Subject Area

Pharmacy and PharmacologyMain Subject Area

Programme overview

Main Subject

Pharmacy and Pharmacology

Degree

Other

Study Level

Masters

Study Mode

On Campus

Students have the option to complete a post-master’s curriculum in clinical trial management in Temple’s School of Pharmacy, offered through the school’s RA and QA graduate program. 


This post-master’s certificate requires the completion of coursework focusing on the tools and information needed to understand how clinical trials must be designed and overseen in the pharmaceutical industry, including writing protocols and consent forms, delving into the requirements of good clinical practices, and managing budgets and data. To apply for this 15-credit program, applicants must hold a master’s degree in a pharmacy-related field and a bachelor of science degree in biochemistry, biology, chemistry, physics or a health-related discipline.


Learning Objectives


Upon completion of the post-master’s certificate, students will understand the


  • basis for new drug discovery;
  • design and implementation of the clinical protocol, its conduct and effective monitoring strategies;
  • auditing of data to ensure the integrity of the trial;
  • bioethics of clinical research;
  • protection of the human research subject;
  • informed consent form and process; and
  • role and responsibilities of the key personnel—the IRB, sponsor, monitor, CRO and the clinical investigator.

Programme overview

Main Subject

Pharmacy and Pharmacology

Degree

Other

Study Level

Masters

Study Mode

On Campus

Students have the option to complete a post-master’s curriculum in clinical trial management in Temple’s School of Pharmacy, offered through the school’s RA and QA graduate program. 


This post-master’s certificate requires the completion of coursework focusing on the tools and information needed to understand how clinical trials must be designed and overseen in the pharmaceutical industry, including writing protocols and consent forms, delving into the requirements of good clinical practices, and managing budgets and data. To apply for this 15-credit program, applicants must hold a master’s degree in a pharmacy-related field and a bachelor of science degree in biochemistry, biology, chemistry, physics or a health-related discipline.


Learning Objectives


Upon completion of the post-master’s certificate, students will understand the


  • basis for new drug discovery;
  • design and implementation of the clinical protocol, its conduct and effective monitoring strategies;
  • auditing of data to ensure the integrity of the trial;
  • bioethics of clinical research;
  • protection of the human research subject;
  • informed consent form and process; and
  • role and responsibilities of the key personnel—the IRB, sponsor, monitor, CRO and the clinical investigator.

Admission Requirements

Jan
Aug

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