About the role
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.
You Might Be a Great Fit If You
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.
Why Centricity Research?
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.
Benefits
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 Ready to Apply?
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.
- 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.