Clinical Research Compliance Analyst
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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.
- Bachelor’s Degree - Working knowledge of the federal regulations governing human subjects research.
License/Certification/Registration Requirements:
Physical Demands:
- CIP or CCRP (or equivalent certification) preferred.
Physical Demands:
- Physical ability and perceptive acuity to perform functions.