Clinical Research Coordinator

Elite Clinical Network is seeking a highly organized Clinical Research Coordinator to support clinical trials and research studies. The role coordinates participant recruitment, consent, data collection, specimen handling, regulatory compliance, study documentation, and communication with sponsors, monitors, and IRBs.

Responsibilities

Coordinate day-to-day clinical research activities to ensure study protocols are followed

Recruit, screen, and enroll study participants

Obtain informed consent and ensure ethical conduct in all study interactions

Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples)

Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs)

Maintain accurate and timely documentation in case report forms and electronic databases

Communicate with sponsors, monitors, and IRBs regarding study progress and compliance

Schedule participant visits and follow-ups; ensure visit windows are met

Ensure proper storage, handling, and accountability of investigational products, if applicable

Maintain regulatory documents and assist with IRB submissions

Preferred

At least 1–2 years of experience in clinical research preferred

Phlebotomy certification or MA certification preferred

Experience working in clinical trials, especially in a hospital or academic setting

Familiarity with IRB processes and clinical trial documentation

Bilingual skills (depending on patient population) may be a plus

At least 1–2 years of experience in clinical research preferred.

Clinical research experience

Phlebotomy certification

Medical assistant certification

Clinical trial experience

Hospital setting experience

Academic setting experience

IRB processes

Clinical trial documentation

Bilingual skills

Company

Network of pharmaceutical research sites for clinical trials

Las Vegas, Nevada, USA

https://eliteclinicalnetwork.com/

Founded in 1993

201-500 employees

Qualifications

Bachelor's degree in a health-related field required

Knowledge of Good Clinical Practice (GCP) and regulatory guidelines

Excellent organizational skills and attention to detail

Strong interpersonal and communication skills

Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms)

Ability to work independently and as part of a multidisciplinary team

8 hour shift

Monday to Friday

Weekends as needed

At least 1–2 years of experience in clinical research preferred

Phlebotomy certification or MA certification preferred

Experience working in clinical trials, especially in a hospital or academic setting

Familiarity with IRB processes and clinical trial documentation

Bilingual skills (depending on patient population) may be a plus

Required skills

Clinical Research, Phlebotomy Certification, Medical Assistant Certification, Clinical Practice (GCP), Regulatory Compliance, Microsoft Office, REDCap, Electronic Data Capture

Preferred skills

Phlebotomy certification or MA certification preferred, Las Vegas, Nevada, USA, https://eliteclinicalnetwork.com/, Growth Stage, Total Funding, $200M, Key Investors, MGG Investment Group, 2023-09-08, Debt Financing· $200M, Recent News, 2025-06-02, Morningstar.com, 2025-04-22, PICANTE Today – Hot News Today, SurgePE Closes Elite Clinical Network Investment, 2024-12-02, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit, Understand your strength & weakness

Experience

1-2 years