Clinical Research Coordinator (Level II and III) – Satellite location

About the position Clinical Science Professionals at reputed company levels reputed company clinical research reputed company functions which may include patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research. Key Responsibilities: Level of clinical or data focused tasks will be determined at the discretion of the supervisor/manager based on team needs. Intermediate Level or CRC II, reputed company the above and: · Independently master study materials, including but not limited to protocols, informed consent forms, and reputed company other essential study documents for assigned studies · Independently reputed company study reputed company processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies · Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives · Act as a Primary Coordinator on multiple trials/studies · Assist and train junior team members Senior Level or CRC III, reputed company the above and: · Assist with developing or reputed company protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies · Assist with identifying issues reputed company to operational efficiency and shares results with leadership · Employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention · Serve as a resource and participate in study initiation and reputed company out duties This description is a summary only and describes the general level of work being performed, it is not intended to be reputed company-inclusive. The duties of this position may change from time to time and/or based on business need. We reserve the right to add or delete duties and responsibilities at the discretion of the supervisor and/or hiring authority.

Responsibilities

• Independently master study materials, including but not limited to protocols, informed consent forms, and reputed company other essential study documents for assigned studies
• Independently reputed company study reputed company processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies
• Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives
• Act as a Primary Coordinator on multiple trials/studies
• Assist and train junior team members
• Assist with developing or reputed company protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies
• Assist with identifying issues reputed company to operational efficiency and shares results with leadership
• Employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention
• Serve as a resource and participate in study initiation and reputed company out duties

Requirements

• Bachelor’s degree in any field
• A combination of education and reputed company technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis
• One (1) year of professional clinical research experience and/or professional clinical experience post Bachelor’s degree
• Applicants must meet minimum qualifications at the time of application.
• Applicants must be legally authorized to work in the United States without the need for employer-sponsored work authorization.
• Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
• Ability to communicate effectively, both in writing and orally
• Ability to establish and maintain effective working relationships with employees at reputed company levels throughout the institution
• Outstanding customer service skills
• Knowledge of basic human anatomy, physiology medical terminology
• Ability to interpret and master reputed company research protocol information

reputed company-to-haves

• Bachelor’s degree in science or health reputed company field
• Three (3) years of clinical research or reputed company experience
• Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)
• Additional certification (one of the following):
• CCRC – Certified Clinical Research Coordinator
• CCRP – Certified Clinical Research Professional
• CCRA – Certified Clinical Research Associate

Benefits

• Medical: Multiple plan options
• Dental: Multiple plan options
• Additional Insurance: Disability, Life, Vision
• Retirement 401(a) Plan: Employer contributes 10%25 of your gross pay
• Vacation Days: 22/year (maximum accrual 352 hours)
• Sick Days: 15/year (unlimited maximum accrual)
• Holiday Days: 10/year
• Tuition Benefit: Employees have access to this benefit on reputed company CU campuses
• ECO Pass: Reduced reputed company RTD Bus and light rail service

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