Regional CRA

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This will be a fully independent home based position  (multiple positions on the west coast, east coast, mid-west and/or south). 

NOTE: This position requires the candidate to have a MINIMUM of 2 years regional monitoring experience in Phase I through IV studies and at least 3 years in the pharmaceutical industry.  If you do NOT meet the minimum requirements, do NOT apply.


This position will be responsible/ accountable for the identification, selection, set-up, monitoring and close down of investigational trial sites in one or more programs.

This person will be completely accountable for the site management and data quality of each site for which they are responsible. They must be able to operate a home based office and be fully functional as a home based monitor/site manager. This would include generating correspondence and reports without administrative help, making one's own travel arrangements, general clerical duties associated with managing a home based office and the ability to anticipate, trouble shoot and resolve various types of problems and issues independently and without peer support. This person will also be expected to develop a rapport with potential investigators, representing many different medical specialties to facilitate the placement of future research studies at institutions and medical centers.

Full Requirements:
  Bachelor Degree or above.  MINIMUM of 2 years regional monitoring experience in Phase I through IV studies and at least 3 years in the pharmaceutical industry. This candidate will be based in their home office and will be required to travel regionally to monitor Phase I through IV studies.  Strong computer literacy (MS Word, MS Excel, MS PowerPoint and MS Outlook (Email and Calendar).

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