Clinical Research Specialist I

What We Offer:

The Clinical Research Assistant I is responsible for the coordination, collection, processing and quality control of clinical trial data under the direct supervision of the Manager Clinical Research. Maintains all research protocol data and compliance reporting. Assists with screening of and consent from patients for research protocol regimens.

Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, quality, compliance and stewardship.

What We're Looking For:

• Education: High School or GED, required. 4 Year / Bachelors Degree, preferred.
• Experience: Clinical Research or healthcare/medical experience preferred. Associate's degree may substitute for 1 year of experience or Bachelor's degree may substitute for 2 years of experience; Master's degree may substitute for 3 years of experience. Certification (ACRP/SOCRA/equivalent) preferred, preferred
• Licensure/Certification/Registration: Valid driver's license in appropriate state,required.
• Additional Skills Required: Must have exceptional organizational and analytical skills. Attention to detail. Self-motivated and able to work independently. Able to meet multiple deadlines for concurrent projects. Work in a team- oriented setting. Must be proficient in Microsoft Office. Must provide own transportation to clinics, hospitals and associated agencies as required. Manual dexterity, prolonged standing or sitting. Able to lift light to medium weight objects which may be bulky and awkward. Ability to travel to developmental, educational and promotional activities. Physical and mental stamina required to function effectively in an environment with multiple fluctuating priorities. Ability to communicate effectively with individuals of all cultures and levels of authority. Exposure to hazardous materials (study agents, biohazards, pathology specimens).