Clinical Research Coordinator(Onsite)

Shift : M-F 7am to 4pm hours may be adjusted by Hiring Division Director

Position Summary:

The Research Coordinator is responsible for coordinating multiple clinical research protocols and serving as a liaison between investigators, sponsors, and internal stakeholders. Under direct supervision, the coordinator will develop a foundational understanding of research regulations and human subject research operations.

Key Responsibilities:

• Adhere to the organization's Code of Conduct and Mission & Value Statement.

• Complete all required training assignments by designated deadlines.

• Perform daily operational tasks for multiple research studies.

• Coordinate communications among site staff, sponsors, and supervisors.

• Work with departments including finance, hospital administrators, and IRB.

• Manage assessment schedules from feasibility through study closeout.

• Review study designs and eligibility criteria with physicians and participants.

• Ensure patient protection through proper informed consent and protocol compliance.

• Maintain accurate data via thorough source document review and entry.

• Create study-specific documentation tools when needed.

• Collect and enter data into case report forms and electronic systems.

• Track and manage drug, device, and supply shipments.

• Ensure timely, accurate data completion and documentation.

• Report and track adverse events, protocol deviations, waivers, and violations.

• Address protocol-related issues with study teams and management.

• Participate in investigator meetings, sponsor calls, and internal CRC meetings.

• Respond to monitoring and audit findings.

Education & Experience:

• Required: Bachelor's degree and at least 1 year of relevant experience

• Preferred: Advanced degree or additional related experience

• Equivalent combination of education and experience accepted

Licenses & Certifications:

• Preferred: Certified Clinical Research Coordinator (CCRC)

Knowledge, Skills & Abilities:

Knowledge:

• Clinical research regulations (ICH, CFR)

• Organizational policies and procedures

• Basic medical terminology

Skills:

• Effective written and verbal communication

• Strong organization and time management

• Clinical procedures: ECG, phlebotomy, specimen processing and shipping

Abilities:

• Strong interpersonal skills

• Self-motivated and detail-oriented

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.