Research Assistant

Responsibilities

Conduct study activities in compliance with GCP, SOPs, and protocols; monitor participant safety; and perform scheduled visits and assessments (e.g., vitals, ECGs)

Support recruitment efforts, screen participants, obtain informed consent, and maintain accurate documentation

Perform delegated clinical tasks such as phlebotomy, sample collection/shipping, point-of-care testing, and investigational product accountability

Complete source documents and CRFs, maintain CTMS records, report adverse events promptly, and ensure investigational product inventory and storage compliance

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

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

Centricity Research offers sponsors and CROs access to clinical research centers and experienced investigators.

Columbus, Georgia, USA

https://www.centricityresearch.com/

Distribution of Different Job Fields Receiving Sponsorship

Represents job field similar to this job

Engineering and Development

Trends of Total Sponsorships

*2021

(1)

Growth Stage

Total Funding

unknown

2023-05-31

Acquired

Leadership Team

Jeff Kingsley

Chief Development Officer and Board member

Joe Surber

Chief Medical Officer

Recent News

24-7 Press Release Newswire

Marquis Who's Who Honors Matthew H. Maxwell, DBA, MS—A Leader in Clinical Research, Growth and Innovation

2025-04-03

Centricity Research Appoints New CEO, CFO to Support Next Phase of Growth

2024-02-22

Qualifications

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

Required skills

Clinical Practice (GCP), Clinical Trial Protocols, Phlebotomy, Electrocardiography (ECG), Point-of-Care Testing, Clinical Data Management Systems, Microsoft Office

Experience

Entry level