Cancer Clinical Trials Coordinator

Charleston Area Medical Center; Charleston (WV); On-site; USD 56,000 - 75,000; Full time

Job summary

Charleston Area Medical Center is seeking a Clinical Research Coordinator for the Cancer Research Center in the Cancer Center Building, US-WV-Charleston. You will coordinate trial protocols, manage data, and support IRB/regulatory activities while communicating with sponsors and PI.

A Master’s degree and 2–3 years of research experience are required, with potential substitution as specified by policy. Responsibilities include regulatory document preparation, budget oversight, patient scheduling,

Qualifications

• Ability to obtain and interpret information to assess patient needs.
• Knowledge of growth and development applicable to patients.
• Understanding of range of treatment needs by patients.

Responsibilities

• Coordinate study protocol requirements and data collection.
• Manage scheduling, visits, procedures, and lab testing for trials.
• Prepare regulatory and budget documents for studies.
• Document visits, CRFs and study progress for sponsors.

Skills

Clinical research coordination

Regulatory compliance

IRB knowledge

Data collection

Budget tracking

Study documentation

Education

Master's Degree (Required)

2-3 years clinical research experience

Master's substitute option with related degree + experience

LPN/CST with 5-7 years clinical experience

Job description

Charleston Area Medical Center is seeking a Clinical Research Coordinator for the Cancer Research Center in the Cancer Center Building, US-WV-Charleston. You will coordinate trial protocols, manage data, and support IRB/regulatory activities while communicating with sponsors and PI.

A Master’s degree and 2–3 years of research experience are required, with potential substitution as specified by policy. Responsibilities include regulatory document preparation, budget oversight, patient scheduling,