Primary Duties and Responsibilities
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This role is an essential part of our Clinical Trials team, providing hands on administrative and logistical support that keeps our research studies running efficiently and in full regulatory compliance. In this position, you will help maintain the accuracy and integrity of clinical trial operations by transporting study samples, entering and updating study data, scanning and organizing key documents, and supporting various day to day research tasks.
This is an excellent opportunity for someone interested in clinical research who enjoys fast paced, detail oriented work and wants to contribute to meaningful, impactful studies that improve patient care.
Salary: $17.90- $47.00 hourly
Job Qualifications
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Required:
- Ability to extract data and organize large databases
- Ability to use Microsoft Word, Excel, and PowerPoint
- Ability to establish and maintain accurate records and data entry
- Ability to prepare data for publication and grant applications
- Ability to generate figures and tables for manuscript publication
- Skill in conducting literature search and retrievals, both through use of bioscience library and on-line service
As a condition of employment, the final candidate who accepts an offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; or have filed an appeal of a finding of substantiated misconduct with a previous employer.