Clinical Research Compliance Analyst

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Compliance/Quality
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18001655 Requisition #
Thanks for your interest in the Clinical Research Compliance Analyst position. Unfortunately this position has been closed but you can search our 101 open jobs by clicking here.
Experience:
  • 2-3 years experience in a healthcare or research setting, with preferred clinical research or IRB experience
  • Excellent writing skills are needed to generate clear, precise, detailed and grammatically correct technical letters, memos, and reports. 
  • Exceptional analytical ability is necessary in order to apply knowledge of federal regulations and institutional policy to research proposals. 
  • Superior organizational skills and attention to accuracy are required in order to effectively and efficiently manage multiple priorities and a high volume workload. 
  • Strong interpersonal and communication skills with a capacity to work well with multiple constituencies of various educational and social backgrounds. 
  • Proficient in the use of multimedia hardware and software applications, including the use of Windows, database, spreadsheet and word processing. 
  • Must be motivated and have the ability to work under pressure to meet deadlines. 
  • Must know when to refer issues to Supervisor and have the ability to make accurate and appropriate independent judgments, but be able to accept direct supervision. 
  • Ability to meet production within established time and quality standards is required. 
Educational Requirements:
  • Bachelor’s Degree - Working knowledge of the federal regulations governing human subjects research.
License/Certification/Registration Requirements:
  • CIP or CCRP (or equivalent certification) preferred.

Physical Demands:
  • Physical ability and perceptive acuity to perform functions.


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