Clinical Research Coordinator: Dallas Trials

Kelly Services; Nevada (IA); Presencial; USD 39 000 - 41 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical benefits

Dental and vision coverage

Transit spending account

Paid holidays

Paid sick leave

Resumo da oferta

Kelly Science & Clinical is seeking a Clinical Research Coordinator for a contract opportunity in the Dallas, TX area. The CRC will support day-to-day coordination of clinical studies, ensuring compliance with protocols and regulatory requirements while delivering quality participant experiences.

The role partners with investigators and study staff to manage enrollment, data collection, and study documentation, following GCP and HIPAA guidelines.

Qualificações

• High school diploma or equivalent required; Associate's degree or higher in a health-related field preferred.
• Previous clinical research experience or foundational knowledge of clinical research strongly preferred.
• Experience with patient care and medical terminology required.
• Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
• Excellent communication and interpersonal skills.
• Proficiency with Microsoft Office and electronic data capture (EDC) systems preferred.
• Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines preferred.
• Experience with participant screening and informed consent is highly desirable.

Responsabilidades

• Coordinate and support clinical research studies in accordance with study protocols and regulatory requirements.
• Screen potential study participants and collect medical histories and other required information.
• Assist with the informed consent process and participant enrollment.
• Schedule study visits, procedures, and participant follow-up activities.
• Collect, document, and maintain accurate source documentation and clinical research data.
• Educate participants on study requirements and respond to study-related questions.
• Monitor study progress and report adverse events, protocol deviations, and other research-related findings.
• Maintain study files and documentation through scanning, uploading, filing, and record management.
• Draw, process, package, and ship laboratory specimens when qualified.
• Follow site SOPs, HIPAA, GCP, FDA regulations, and other applicable research standards.
• Support additional research activities as assigned.

Conhecimentos

Clinical research

Patient care

Medical terminology

Organizational skills

Communication skills

EDC systems

Microsoft Office

GCP knowledge

HIPAA knowledge

Informed consent

Formação académica

High school diploma or equivalent

Associate's degree or higher preferred

Ferramentas

Microsoft Office

EDC systems

Descrição da oferta de emprego

Kelly Science & Clinical is seeking a Clinical Research Coordinator for a contract opportunity in the Dallas, TX area. The CRC will support day-to-day coordination of clinical studies, ensuring compliance with protocols and regulatory requirements while delivering quality participant experiences.

The role partners with investigators and study staff to manage enrollment, data collection, and study documentation, following GCP and HIPAA guidelines.