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Associate Clinical Scientist  


The Associate Clinical Scientist will serve as a clinical scientist providing pharmacology support and execution of the development, update and maintenance of the TRHC's clinical decision support system (CDSS) of drug-drug interactions based on drug pharmacokinetics properties. The successful candidate will have a working knowledge of clinical pharmacology, drug metabolism, drug transporters, and related pharmacokinetics principles. This person will work in collaboration with other research and clinical scientists in the Precision Pharmacotherapy Research & Development institute for the integration of generated information and of knowledge into the overall program strategies, to improve the efficiency of the TRHC's CDSS, improve our mechanistic understanding and provide scientific rationale. This individual will also work in close collaboration with the TRHC academy to provide advanced training and review educational programs related to the TRHC's CDSS. This is an exciting opportunity to be part of a high-impact clinical pharmacology team and collaborative setting.

TRHC Scientific Precision Pharmacotherapy Research & Development Institute (SPPRDI) is committed to the development of proprietary products, their validation and recognition by the scientific and regulatory communities to optimize medication regimen in order to improve patient outcomes, reduce utilization of various healthcare services, lower healthcare costs, and manage risk.

  • Accountable and responsible for ensuring maintenance and update of drugs into the CDSS.
  • Performs, integrates and interpret PK analysis including pre-clinical and clinical studies.
  • Interpret enzymatic assays, in vitro/ex vivo drug metabolism studies. Integrate metabolism and transporter data to provide mechanistic interpretation into the CDSS.
  • Fully knowledgeable about PK's drugs; to address, identify and resolve scientific issues.
  • Contributes to expert pharmacology input into educational training programs and materials.
  • Complies with all applicable regulations, maintains proper records in accordance with SOPs and policies

Position Requirements


  • PharmD or MD equivalent and PhD from an accredited institution in Clinical pharmacology, Pharmacokinetics, Drug metabolism, or other relevant fields or equivalent experience in related fields.


  • Experience in clinical pharmacology research.
  • Experience in research (post-doctoral formation/fellowship; up to 2 years) would be advantageous.

Specific Skills:

  • An in depth knowledge of drug metabolizing enzymes and transporters would be considered highly beneficial.
  • Demonstrated ability and strong understanding with preclinical and clinical PK data.
  • Demonstrates ability to drive for results independently.
  • Participates in team for ensuring valid methods and in assessing review process.
  • Applicant should be organized, self-motivated and capable of working autonomously and in a collaborative environment.
  • It would be advantageous for the candidate to have knowledge on pharmacogenomics.

Full-Time/Part-Time Full-Time  
Shift -not applicable-  
Position Associate Clinical Scientist  
Post Internal Days 0  
Number of Openings 4  
Location Tabula Rasa, Lake Nona, FL  
About the Organization  
EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.  
Cell None Specified 

HoursPerWk None Specified 

supervisorUID None Specified 

This position is currently accepting applications.

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