Clinical Research Coordinator
Listed on 2026-07-01
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Research/Development
Clinical Research, Research Assistant/Associate, Medical Science, Research Scientist -
Healthcare
Clinical Research, Medical Science
Clinical Research Coordinator I
The Clinical Research Coordinator I focuses on a personalized medicine clinical research study. Responsibilities include interviewing and consenting subjects for participation, arranging collection of blood samples, data collection, data entry and data analysis. Other tasks include preparing summaries of data and related literature related to the current research, and help in the generation of reports, posters, abstracts, and articles related to the research project.
These positions are a wonderful opportunity for those anticipating pursuing a degree in Medicine.
- Interviewing and consenting subjects for participation.
- Arranging collection of blood samples.
- Data collection, data entry and data analysis.
- Preparing summaries of data and related literature related to the current research.
- Assist in the generation of reports, posters, abstracts, and articles related to the research project.
- Accountable for all tasks in basic clinical studies.
- Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
- Performs other related work as needed.
Education:
Minimum requirements include a college or university degree in related field.
Work Experience:
Minimum requirements include knowledge and skills developed through < 2 years of work experience in a related job discipline.
Certifications:
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Preferred QualificationsEducation:
- Bachelor's degree.
Experience:
- Knowledge of medical terminology/environment.
- Ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.
- Ability to communicate with tact and diplomacy.
- Strong organizational skills.
- Strong communication skills (verbal and written).
- Excellent interpersonal skills.
- Strong data management skills and attention to detail.
- Knowledge of Microsoft Word, Excel and Adobe Acrobat.
- Ability to understand complex documents (e.g., clinical trials).
- Ability to handle competing demands with diplomacy and enthusiasm.
- Ability to absorb large amounts of information quickly.
- Adaptability to changing working situations and work assignments.
- Resume (required)
- Cover Letter (required)
When applying, the document(s) MUST be uploaded via the My Experience page, in the section titled Application Documents of the application.
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