Clinical Research Coordinator

ESSENTIAL DUTIES AND RESPONSIBILITIES

• Provide assistance in the administrative, technical and scientific day-to-day operation of the study to assure project goals and timelines are met, quality data is collected and managed, and to assure participant and/or data confidentiality.
• Conduct clinical research as outlined in the study protocol. Maintain knowledge of clinical research issues. Follow GCP guidelines. Implement confidentiality and privacy regulations.
• Evaluate protocols, assist in study selection, correspond/coordinate with the sponsor/CRO and prepare study budgets.
• Support and assist Research personnel in the operation of equipment used in clinical trials.
• Support the development of Quality Assurance procedures, and assist with the monitoring of data collection and data transfers.
• Aid in the preparation of annual IRB reviews.
• Support the Project Director, Clinic Coordinator, or PI in the administration of the grant/contract per federal rules and regulations and/or specific grant/contract language.
• Understand the operational budget and sub-contracts; track documentation and authorization of payment of study related bills.
• Provide assistance in the preparation of project reports for PI review and approval.
• Recruit study participants to a broad range of studies using specific study protocols to contact, screen, and determine eligibility and schedule appointments with study participants.
• Collect, edit and record/enter study data via interview, structured interview, questionnaire, medical record review, and basic clinical measurements for complex study protocols, and perform technical duties as assigned.
• Support orientation and structured intervention sessions in accordance with technical training and certification(s).
• Assist with case management activities to support the work of the project(s).
• Support the process of summarizing and sharing project information with other sites.
• Aid in the tracking of papers in process for projects, with planning for project papers and posters to be presented at national and international conferences.
• Adhere to all safety policies and procedures in performing job duties and responsibilities while supporting a culture of high quality and great customer service.
• Perform other duties in support of clinical trials services as assigned.

QUALIFICATIONS

• Demonstrated interpersonal, communication and interviewing skills with people of all ages.
• Organized, detail oriented, self-directed and dependable.
• Able to prioritize work, solve problems and work independently.
• Able to function in a team environment and use negotiation skills.
• Favorable result on background check required.
• Must be able to provide proof of identity and right to work in the United States.