Clinical Research Intern
- Employer
- Westat
- Location
- Rockville , MD
- Posted
- Jan 14, 2023
- Closes
- Feb 08, 2023
- Function
- Analyst, Research, Entry Level and Intern
- Industry
- Research
- Career Level
- Experienced (Non-Manager)
- Hours
- Full Time
Westat's 9-week summer internship experiences will be hosted virtually, or on-site at our U.S. office-based locations.
Our interns can expect to work 40 hours per week, Monday through Friday. The program will begin on Monday, June 5, 2023, and end on August 4, 2023.
During the summer internship program, you will be assigned a project deliverable and will present during the final week of the program.
You will also attend educational programs and networking events.
This position is based on-site in Rockville, Maryland. The pay rate for this role is $20/hr.
Interns are responsible for securing their own housing should they select an on-site role.
As a Clinical Research intern, you will work collaboratively with project staff on HIV protocol development and implementation activities; contribute to gathering clinical site performance data and populate site performance database in advance of presenting to the client.
Please include a cover letter when applying to this role.
Job Responsibilities:
Basic Qualifications:
Our interns can expect to work 40 hours per week, Monday through Friday. The program will begin on Monday, June 5, 2023, and end on August 4, 2023.
During the summer internship program, you will be assigned a project deliverable and will present during the final week of the program.
You will also attend educational programs and networking events.
This position is based on-site in Rockville, Maryland. The pay rate for this role is $20/hr.
Interns are responsible for securing their own housing should they select an on-site role.
As a Clinical Research intern, you will work collaboratively with project staff on HIV protocol development and implementation activities; contribute to gathering clinical site performance data and populate site performance database in advance of presenting to the client.
Please include a cover letter when applying to this role.
Job Responsibilities:
- Logistics support for meeting planning
- Meeting summaries
- Organizing project files Clinical site performance assessments
- Establishment of protocol development plans and timelines
Basic Qualifications:
- Currently enrolled in an undergraduate program pursuing an associate or Bachelor degree in public health, biology or a health-related area
- Experience with research protocol development and implementation; good clinical practice guidelines; elements of quality clinical trials performance
- Demonstrated communication skills, adept at organization and detail oriented
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