Role OverviewAssists the Clinical Research Coordinator and the principal investigator with administering activities to facilitate clinical research, which may include working with an affiliate or collaborating research sites.
What You Will Do
Assists with the creation and completion of study related documents, completes regulatory submissions, acts as a secondary liaison with sponsors, and completes case report forms.
Why It Might Be a Fit
Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor. Must have knowledge of Microsoft Office and electronic case report form systems.
Requirements
- High school diploma or general education degree (GED); or two to four years related experience and/or training; or equivalent combination of education and experience.
- Clinical research certification preferred
- Ability to demonstrate competence in oral and written communication
- Bilingual (English/Spanish) required
- Must be organized, attentive to detail, and possess a positive, friendly, and professional demeanor
- Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
- Medical knowledge, including medical terminology
- Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals
- Ability to write routine reports and correspondence
- Ability to speak effectively before groups of customers or employees of the organization
- Must have knowledge of Microsoft Office Word, Microsoft Excel, Internet Explorer, Google Chrome, Mozilla Firefox, web-based enterprise solutions, and Electronic Case Report Form systems
Benefits
- 401k
- Medical, dental, vision, long term disability, short term disability, FSA, and life insurance
- 3 weeks of paid time off
- 14 paid company holidays
- Scrub voucher (specific positions apply)
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