Clinical Research Associate II
New
P
Precision Medicine GroupClinical Trial Services
This remote role requires someone living in Texas or CaliforniaFull-TimeMiddle
Salary91,500 - 137,300 USD per year
Apply NowOpens the employer's application page
Job Details
- Languages
- English
- Experience
- Two (2) years or more as a CRA
- Required Skills
- GCP
Requirements
- 4-year college degree or equivalent experience in a scientific or healthcare discipline
- Two (2) years or more as a CRA in a CRO or pharmaceutical/biotech industry
- Experience monitoring oncology trials
- Evidence of a client focused approach
- Proficiency with computerized information systems, electronic spreadsheets, and word processing
- Ability to travel overnight up to 60% on average
- Fluency in English
Responsibilities
- Oversee study site management to ensure patient safety and data quality.
- Provide guidance for audit readiness and follow-up actions.
- Manage site start-up procedures including investigator recruitment and regulatory document collection.
- Assist in the negotiation of study budgets and execution of investigator contracts.
- Independently conduct pre-study, initiation, routine monitoring, and close-out visits.
- Document monitoring activities via trip reports, confirmation letters, and communication logs.
- Perform investigational product (IP) inventory and reconciliation.
- Review data, including remote EDC CRF and patient profiles, and resolve queries.
- Identify and process Serious Adverse Events (SAE) according to protocol.
View Full Description & ApplyYou'll be redirected to the employer's site
