Clinical Research Specialist - Trial Coordination

East Carolina University; Greenville (NC); On-site; USD 54,000 - 60,000; Full time

Job summary

East Carolina University’s Internal Medicine Hematology and Oncology Division seeks a Clinical Research Specialist to manage designated clinical trials under the supervision of the Social/Clinical Research Manager. You will collaborate with investigators, coordinate study activities, collect data, and ensure regulatory compliance across multiple protocols.

Key duties include coordinating patient recruitment and enrollments, handling data entry and lab shipments, and supporting audit readiness.

Qualifications

• Bachelor's degree in a related field and one year of related training or experience.
• Clinical trial or data collection experience preferred.

Responsibilities

• Study coordination, recruitment, screening and accrual of potential patients.
• Data entry and query resolution along with lab processing and shipment.
• Provide guidance to staff and investigators regarding regulatory and compliance issues.
• Assist with audit preparation and review trial related documents for accuracy and completion.

Skills

Study coordination

Data entry

Regulatory compliance

Audit preparation

Education

Bachelor's degree in related field

Job description

East Carolina University’s Internal Medicine Hematology and Oncology Division seeks a Clinical Research Specialist to manage designated clinical trials under the supervision of the Social/Clinical Research Manager. You will collaborate with investigators, coordinate study activities, collect data, and ensure regulatory compliance across multiple protocols.

Key duties include coordinating patient recruitment and enrollments, handling data entry and lab shipments, and supporting audit readiness.