Clinical Research Associate II
New
P
Precision for MedicineClinical Research
This remote role requires someone living in Texas or CaliforniaFull-TimeMiddle
Salary91,500 - 137,300 USD per year
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Job Details
- Languages
- English
- Experience
- Two (2) years or more as a CRA in either a CRO or pharmaceutical/ biotech industry
- Required Skills
- GCP
Requirements
- 4-year college degree or equivalent experience in a scientific or healthcare discipline.
- Two years or more as a CRA in a CRO or pharmaceutical/biotech industry.
- Experience monitoring oncology trials.
- Evidence of a client focused approach.
- Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail.
- Ability to travel overnight (up to 60% average).
- Fluency in English.
- Excellent communication and organizational skills.
Responsibilities
- Oversees all aspects of study site management to ensure patient safety and data quality.
- Conducts pre-study, initiation, routine monitoring, and close-out visits.
- Updates, tracks and maintains study specific trial management tools and status reports.
- Verifies the process of obtaining informed consent and assesses safety factors.
- Performs investigational product (IP) inventory, reconciliation and reviews storage.
- Performs data review activities, including remote EDC CRF and patient profiles review.
- Identifies and processes Serious Adverse Events (SAEs).
- Prepares and submits accurate and timely monitoring reports from site visits.
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