Onsite Clinical Research Assistant – Participant Focused

Centricity Research; Morehead City (NC); On-site; USD 20,000 - 29,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Enhanced Employee Assistance Program (

Flexible PTO and paid holidays

Continuing education reimbursement

401(k) with company match

Job summary

Centricity Research is seeking a Research Assistant for our Morehead City, North Carolina site. This onsite role supports study execution from screening to data collection. You’ll work with investigators, CRCs, and the site team to ensure safety, protocol compliance, and accurate documentation.

The role is 100% onsite with a standard Monday–Friday schedule. Remote or hybrid arrangements are not available. We offer comprehensive benefits and ongoing opportunities in clinical research across

Qualifications

• Degree or equivalent hands‑on experience in a health, science, or research field.
• Strong attention to detail with documentation accuracy.
• Able to adapt in a fast-paced clinical research environment.
• Effective communication with participants, colleagues, and partners.

Responsibilities

• Conduct study activities in compliance with GCP/SOPs and protocols; monitor participant safety.
• Support recruitment, screen participants, obtain informed consent, and document.
• Perform delegated clinical tasks such as phlebotomy, sample collection/shipping, and point‑of‑care testing.
• Complete source documents/CRFs, maintain CTMS records, report adverse events promptly.
• Prepare for monitoring visits and audits, maintain ISF, assist with scheduling and check‑in/out.

Skills

Attention to detail

Clear and professional communication

Team player with ability to work solo

Tech-savvy with Microsoft Office and E

Education

Health/Science degree or equivalent clinical experience

Tools

Microsoft Office

Job description

Centricity Research is seeking a Research Assistant for our Morehead City, North Carolina site. This onsite role supports study execution from screening to data collection. You’ll work with investigators, CRCs, and the site team to ensure safety, protocol compliance, and accurate documentation.

The role is 100% onsite with a standard Monday–Friday schedule. Remote or hybrid arrangements are not available. We offer comprehensive benefits and ongoing opportunities in clinical research across