Job Description

Clinical Research Coordinator

• Newport Beach, CA
• Additional site coverage needed for Mission Viejo, California
• Full-time/Direct Hire
• This position offers a competitive rate of $28/hr - $35/hr plus occasional overtime

Kelly Science and Clinical is hiring a Clinical Research Coordinator for one of our clients who has been recognized as one of the largest independent, multi-site clinical research companies in the US. This position is on-site and located in Newport Beach, CA .

Job Description

The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

Essential Duties and Responsibilities:

• Assisting trial Investigator in screening and reviewing potential study participants eligibility
• Maintaining case report forms, charts and documentation
• Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
• Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
• Collecting and entering data as necessary
• Assist management with potential new hire selection and shadowing process
• Assist with study start-up, maintenance, and close-out of studies as needed for those on the team
• Ability to be flexible with study assignments

Qualifications

• Clinical Research Coordinator with 1-2 years of experience
• Phlebotomy experience and current certification/license to perform phlebotomy in the state of California is preferred
• Excellent verbal & written communication skills
• Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-tasking
• Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines
• Extensive clinical trial knowledge through education and/or experience
• Successful completion of GCP Certification and Advanced CRC preferred
• Detail-oriented
• Familiarity with the Code of Federal Regulations as they pertain to human subject protection
• Strong interpersonal skills

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