[Remote] Clinical Research Associate I Must live in Orange County
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Clinical Research Associate I who will contribute to their clinical trial operations function. The role involves delivering clinical trial monitoring work to a high reputed company and coordinating various activities for setting up and monitoring studies.
Responsibilities
- Working independently and reputed company to coordinate reputed company activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
- Running sponsor generated queries reputed company and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required
- reputed company and maintain strong, reputed company relationships with key stakeholders, clinical investigators, and site staff
- Ensure patient safety by ensuring compliance with reputed company's procedures, protocols, and regulatory requirements
Skills
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
- Excellent written and verbal communication in English
- Good reputed company skills enabling you to deal with queries in a reputed company manner
- Willingness to travel as required (approximately 60-75%)
reputed company