Clinical Research Coordinator: Trials & Patient Care Lead

West Virginia University; Morgantown (WV); Presencial; USD 52 000 - 68 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

37.5-hour work week

13 paid holidays

24 annual leave days per year

18 sick days per year

Health insurance

Retirement savings with 6% match

Wellness programs

Resumo da oferta

West Virginia University’s Rockefeller Neuroscience Institute seeks a Clinical Research Coordinator to support Phases I–IV trials. The role coordinates research activities, ensures protocol compliance, and maintains data integrity while collaborating with investigators, staff, and sponsors.

Responsibilities include consent, ongoing participant education, and adherence to regulatory standards. The institution emphasizes work-life balance with generous benefits and a full-time schedule in

Qualificações

• Bachelor's degree from an allied health discipline, or related medical field such as nursing, medical technology, or pharmacy.
• A minimum of two years of experience in clinical settings or clinical research.
• Equivalents considered with related education and experience.

Responsabilidades

• Ensure protocol conduct and regulatory compliance across institutional, state, federal, and international levels.
• Coordinate with investigators, research staff, pharmacy, and clinical teams to implement and conduct trials.
• Monitor activities through internal and external audits/oversight (FDA, IRB, QA).
• Educate staff on study procedures and monitor protocol adherence throughout the lifecycle.
• Assist with recruitment strategy development and participant education/consent processes.

Conhecimentos

Clinical research

GCP/IRB knowledge

Formação académica

Bachelor's degree in allied health or related field

Descrição da oferta de emprego

West Virginia University’s Rockefeller Neuroscience Institute seeks a Clinical Research Coordinator to support Phases I–IV trials. The role coordinates research activities, ensures protocol compliance, and maintains data integrity while collaborating with investigators, staff, and sponsors.

Responsibilities include consent, ongoing participant education, and adherence to regulatory standards. The institution emphasizes work-life balance with generous benefits and a full-time schedule in