Job Description

• Participates in the design, administration and monitoring of clinical trials.
• Responsibilities:
• Plans, organizes, performs and monitors daily project protocols.
• Collects, prepares and maintains required research documentation, such as informed consent records, case records, clinical notes and medical reports.
• Reports and assists with the management of protocol deviations, adverse events and other project-related issues.
• Assists with the preparation and delivery of internal and external presentations, conference reports and lectures, and publishing submissions.
• Understanding of the Food and Drug Administration (FDA) rules is beneficial.

• High School diploma equivalency with 2 years of cumulative experience
• OR
• Associate degree/Technical degree
• OR
• 4 years of applicable cumulative job specific experience required.

Preferred skills:

• Bachelors degree, experience with statistical analysis, attention to detail, adaptability, dependability, communication and interpersonal skills are preferred.
• Critical thinking skills required.

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