We are actively looking for:
SR. CRA, CRA II, CRA 1
Job Description
Key Responsibilities:
A brief summary of duties you will be involved in:
- Site management and site staff performance including monitoring all types of clinical trials ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
- Data Handling, Reporting and Tracking & administrative tasks
- You would also perform management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines
Qualifications
We are seeking candidates with the following key attributes:
To succeed in this role you will need the following skills/experience:
- Education – BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
- Moderate practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
- Thorough understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines
- Good command of written and spoken English language
Primary Location
US – All
Travel
Yes, 70 % of the Time
