Clinical Trials Research Specialist II

CO040 Memorial Regional Hospital; United States; On-site; USD 70,000 - 90,000; Full time

Job summary

Memorial Healthcare System is seeking a Clinical Research Coordinator to conduct Phase 1-4 clinical trials, screen and consent patients, and collect study data in EPIC. The role requires collaborating with a multidisciplinary team and maintaining sponsor data quality across trials.

Role emphasizes adherence to Good Clinical Practice, regulatory compliance, and thorough documentation of visits, adverse events, and study results at Memorial Regional Hospital.

Qualifications

• One year of clinical experience.
• At least two years of clinical research experience.
• Ability to travel for protocol-related investigator meetings.

Responsibilities

• Coordinate activities of multidisciplinary team and patient visits.
• Document patient/study results in electronic medical record (EPIC).
• Screen and consent patients using GCP guidelines.
• Provide patient and family education regarding protocol drugs and procedures.
• Obtain medical history and monitor patient care and side effects.
• Initiate, monitor and close visits with sponsors.
• Ensure compliance with local, state and federal regulations.
• Assist with audits and respond to sponsor data queries.
• Process and ship study specimens.

Skills

Accountability

Accuracy

Customer service

Relationship building

Effective communication

Research project management

Research reporting

Adaptability

Professional conduct

Attention to standards

Education

Accredited Program

Foreign MD Degree

Classroom Training

RN Compact License

Compact RN Multistate

RN License

State of Florida

Tools

EPIC

GCP knowledge

Job description

Memorial Healthcare System is seeking a Clinical Research Coordinator to conduct Phase 1-4 clinical trials, screen and consent patients, and collect study data in EPIC. The role requires collaborating with a multidisciplinary team and maintaining sponsor data quality across trials.

Role emphasizes adherence to Good Clinical Practice, regulatory compliance, and thorough documentation of visits, adverse events, and study results at Memorial Regional Hospital.