Job expirat
As a CRA you will be responsible for 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. It will include 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.
We are seeking candidates with the following key attributes:
• 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
• Experience or education indicates a sound basic knowledge of medical and pharmaceutical terminology.
You will also have:
• Excellent verbal and written communication skills, excellent organizational, record retention, time management, decision making, customer service, and interpersonal skills
• Good command of written and spoken English language
• Ability to travel domestically and internationally as required
• ACRP CCRA or equivalent certification/credentials strongly preferred
INC Research is a top-tier therapeutically focused global clinical research organization (CRO) providing a
complete range of Phase I – Phase IV clinical development services for the world’s biopharmaceutical
companies. We proudly boast 43 of the world’s top 50 pharmaceutical companies as our customers.
With approximately 5,000 employees across six continents and experience spanning more than 100
countries, we provide significant scale, scope and expertise to deliver innovative clinical development
approaches and strategic alliances that meet the needs of our customers.