Clinical Research Associate I FSO
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Job Location:
Monthly Salary:
Posted on:
23 hours ago
Vacancies:
1 Vacancy
Job Summary
WHAT YOU WILL DO
You will utilize your skills knowledge and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.
You will be responsible for (but not only):
- All aspects of study site monitoring including routine monitoring and close-out of clinical sites maintenance of study files conduct of pre-study and initiation visits; liaise with vendors; and other duties as assigned -
- All aspects of site management as prescribed in the project plans
- General On-Site Monitoring
Requirements:
- University or college degree or certification in a related allied health
profession from an appropriately accredited institution (e.g. nursing licensure) - 1-3 years of Clinical Monitoring experience
Experience (Minimum Required):
- Six (6) months experience in a related role (e.g. site management in-house CRA study coordinator research nurse etc.).
- Basic understanding of Regulatory Guidelines.
- Ability to work within a project team.
- Good planning organization and problem-solving skills.
- Good computer skills with good working knowledge of a range of computer packages.
- Works efficiently and effectively in a matrix environment.
- Valid Drivers License.
Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Key Skills
- CSS
- Cloud Computing
- Health Education
- Actuary
- Building Electrician
