Clinical Director for Pharmaceutical Projects

23 hours ago


Gainesville, Florida, United States Maxis Clinical Sciences Full time

Job Summary

This is a highly specialized role that involves providing medical oversight of clinical trials, ensuring compliance with regulatory requirements and company SOPs. The ideal candidate will have extensive experience in treating patients in the specialty or sub-specialty associated with their training.

Key Responsibilities:

  • Manages all medical aspects of contracted tasks across the pharmaceutical product life-cycle.
  • Provides medical consultation to team members and answers study-related medical questions.
  • Monitors safety variables and discusses medical concerns with principal investigators and clients.
  • Performs data review as specified in the client contract and data validation manual.
  • Manages signal detection activities and medically reviews adverse event and serious adverse event data.

Requirements:

  • MD or equivalent required.
  • Candidates should have at least one of the following: clinical experience in treating patients in the specialty or sub-specialty associated with the applicants training (comparable to 3 years); suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 3-5 years) in the industry; direct experience in safety/Pharmacovigilance (comparable to 3 years).
  • In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Benefits:

  • Competitive salary: $150,000 - $200,000 per annum.
  • Opportunity to work on high-profile clinical trials.
  • Collaborative and dynamic work environment.
  • Professional development opportunities.


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