Client is a growing pharmaceutical company located in with a product on the market and several late stage small molecule drug candidates in clinical development.  Position requires approx 40-60% travel and will be based regionally OR at company’s corporate office in Houston.  Regional candidates must reside in or near large cities with major airports.

Regional CRA - Primary responsibilities will be monitoring and management of study site activities: including communication of study priorities, providing directions and training to research staff, interfacing with investigators and their staff, reviewing study documentation and the review and collection of patient data

Requirements:

• BS/BA Degree or equivalent in a scientific, clinical or health-related discipline


• 3+ years experience clinical research/CRA experience, preferably in a regional role


• Ability to evaluate and analyze clinical data, assist in drafting or preparing study specific documents, coordinate activities of associates and investigators to ensure compliance with protocol and overall clinical objectives, and compliance with applicable regulatory requirements

To be considered for this opportunity, please send a MS Word Version of your CV to christy@albrecht-assoc.com along with your contact information and a good time to reach you.