Highlights
About Our Client
Our client is a long standing clinical research site in the Columbus, OH area that takes a truly unique patient-centric, service-oriented, approach to clinical research. Their reputation for excellence has been built across over 20 therapeutic areas, over 15 physicians, and over 550 completed trials! They are looking to expand their team with a skilled clinical research coordinator!
Responsibilities
As a CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!
Qualifications:
...Master's degree desired. Bachelor's. Degree in Finance or Business is also acceptable. Minimum of four years' work experience in managing BMS, HVAC, Industrial Controls / Automation, or similar discipline projects. Microsoft Project (or similar); experience with Smartsheets...
...four years of experience in the following areas: National Interest Waivers (NIW) PERM Labor Certifications EB-5 Investor Visas E-1 and E-2 Treaty Trader/Investor Visas L-1A and L-1B Intracompany Transferee Visas O-1 Extraordinary Ability Visas H-1...
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...The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination of clinical trials at the site level, ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. The CRC acts as the primary liaison...