What are the responsibilities and job description for the Research Assistant position at Centricity Research?
Join Us at Centricity Research!
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
About The Role
We’re looking for a Research Assistant (RA) to support the successful execution of clinical research studies from start to finish. In this role, you’ll work closely with Investigators, Clinical Research Coordinators (CRCs), and the wider site team to ensure studies run smoothly, safely, and in full compliance with protocol and regulations. This hands-on role is varied – some days you’ll recruit and screen participants, other days you’ll collect data, process samples, or keep study documentation organized and accurate. Your work will directly contribute to advancing clinical research that makes a difference in patients’ lives.
⚠️ Please Note: This role is 100% onsite in Morehead City, North Carolina and requires working Monday through Friday, 40-hour work weeks. Remote and hybrid work arrangements are not available.
What You’ll Do
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
We’d love to hear from you – apply now!
We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.
Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient; pharmaceutical, biotechnology, and medical device trials.
About The Role
We’re looking for a Research Assistant (RA) to support the successful execution of clinical research studies from start to finish. In this role, you’ll work closely with Investigators, Clinical Research Coordinators (CRCs), and the wider site team to ensure studies run smoothly, safely, and in full compliance with protocol and regulations. This hands-on role is varied – some days you’ll recruit and screen participants, other days you’ll collect data, process samples, or keep study documentation organized and accurate. Your work will directly contribute to advancing clinical research that makes a difference in patients’ lives.
⚠️ Please Note: This role is 100% onsite in Morehead City, North Carolina and requires working Monday through Friday, 40-hour work weeks. Remote and hybrid work arrangements are not available.
What You’ll Do
- Study Protocol & Safety: Conduct study activities in compliance with GCP, SOPs, and protocols; monitor participant safety; and perform scheduled visits and assessments (e.g., vitals, ECGs).
- Recruitment & Enrollment: Support recruitment efforts, screen participants, obtain informed consent, and maintain accurate documentation.
- Study Visit Execution: Perform delegated clinical tasks such as phlebotomy, sample collection/shipping, point-of-care testing, and investigational product accountability.
- Data Integrity & Compliance: Complete source documents and CRFs, maintain CTMS records, report adverse events promptly, and ensure investigational product inventory and storage compliance.
- Site & Administrative Support: Prepare for monitoring visits and audits, maintain ISF, organize exam rooms and labs, assist with scheduling and participant check-in/out, and support outreach events.
- Have a degree in a health, science, or research-related field or equivalent hands-on experience in a healthcare or clinical setting.
- Are comfortable with clinical tools like blood pressure monitors, ECG machines, or point-of-care testing devices (or are eager to learn).
- Have strong attention to detail and can maintain accurate, compliant documentation.
- Enjoy working in a fast-paced environment with changing priorities.
- Communicate clearly and professionally with participants, colleagues, and external partners.
- Are tech-savvy and comfortable navigating Microsoft Office and clinical data systems.
- Thrive in a team environment but can also work independently.
- Bring a proactive, problem-solving mindset to every challenge.
Our Mission
We connect people to scientific advancements through groundbreaking research within a deeply human experience.
Our Core Values
- Quality: We aim for excellence and integrity in everything we do - because lives depend on it.
- Care: We show up for each other, our customers, and our mission - always going the extra mile.
- Be the Change You Seek: We're adaptable, forward-thinking, and constantly improving - for the betterment of all.
- One Team: We collaborate, support one another, and succeed together.
- Grow for Good: We grow with purpose - to expand access to research and improve global health.
- Own It: We take initiative, deliver results, and follow through - with passion and accountability.
- Comprehensive health, dental, and vision insurance
- Enhanced EAP – mental health support
- Flexible PTO paid holidays
- Continuing education reimbursement
- 401(k) / RRSP with company match and immediate vesting
We’d love to hear from you – apply now!
We’re an equal opportunity employer committed to building a diverse and inclusive workplace. We welcome applicants from all backgrounds and will provide accommodations during the hiring process upon request.