Clinical Trials Coordinator - Recruitment & Data

East Carolina University; South Carolina; On-site; USD 42,000 - 79,000; Full time

Job summary

East Carolina University (ECU) seeks a Social Clinical Research Specialist to manage designated clinical trials under the Social/Clinical Research Manager. You will collaborate with investigators, collect and record data, handle project administration, and communicate with stakeholders to ensure protocol adherence.

Responsibilities include coordinating studies, data entry, regulatory guidance, and audit preparation, with a typical Monday–Friday schedule and daytime hours.

Qualifications

• Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience.
• All degrees must be received from appropriately accredited institutions.
• License or Certification required by statute or regulation: None

Responsibilities

• Study coordination, recruitment, screening and accrual of potential patients (60%).
• Data entry and query resolution along with lab processing and shipment (30%).
• Provide guidance to staff and investigators regarding regulatory and compliance issues (5%).
• Assist with audit preparation and review trial related documents for accuracy and completion (5%).

Skills

Study coordination

Data entry

Regulatory compliance

Education

Bachelor’s degree in a related field

Job description

East Carolina University (ECU) seeks a Social Clinical Research Specialist to manage designated clinical trials under the Social/Clinical Research Manager. You will collaborate with investigators, collect and record data, handle project administration, and communicate with stakeholders to ensure protocol adherence.

Responsibilities include coordinating studies, data entry, regulatory guidance, and audit preparation, with a typical Monday–Friday schedule and daytime hours.