Lead Multitrial Clinical Research Coordinator - On Site

IQVIA LLC

Lexington (KY)

On-site

USD 44,000 - 111,000

Full time

14 days+
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Job summary

IQVIA, a leading global provider of clinical research services, partners with Avacare SMO in Lexington, Kentucky to offer Clinical Research Coordinators a dynamic on-site role across multiple trials. You’ll manage patient recruitment, consent, regulatory documentation, and site audits while coordinating study activities end-to-end.

As CRC, you’ll collaborate with investigators, sponsors, and monitors, mentor junior staff, and gain exposure to CTMS, eCRFs, and Microsoft Office tools.

Qualifications

  • Hands-on clinical skills including vital signs, phlebotomy, ECGs, and lab processing.
  • Solid understanding of site operations and the drug development process.
  • CRC I: 1-3 years at a clinical investigative site with participants.
  • CRC II: 3 years as a CRC at a clinical investigative site with participants.
  • Strong written and verbal communication, with attention to detail and time management.
  • Proficient with CTMS, eCRFs, and Microsoft Office tools.

Responsibilities

  • Recruit and consent participants for trials.
  • Maintain regulatory documentation and conduct site audits.
  • Coordinate 2–6 trials across varying complexity.
  • Mentor junior staff and contribute to internal training.
  • Collaborate with investigators, sponsors, and monitors.

Skills

Clinical skills
Site operations
CRC I experience
CRC II experience
Communication & documentation
CTMS/eCRF proficiency

Tools

CTMS
eCRFs
Microsoft Office

Job description

IQVIA, a leading global provider of clinical research services, partners with Avacare SMO in Lexington, Kentucky to offer Clinical Research Coordinators a dynamic on-site role across multiple trials. You’ll manage patient recruitment, consent, regulatory documentation, and site audits while coordinating study activities end-to-end.

As CRC, you’ll collaborate with investigators, sponsors, and monitors, mentor junior staff, and gain exposure to CTMS, eCRFs, and Microsoft Office tools.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

On-Site Senior Research Coordinator: Clinical Trials Lead
On-Site Senior Research Coordinator: Clinical Trials Lead

IQVIA • Lexington (KY)

On-site
USD 44,300 - 110,500
Clinical Research Coordinator: Lead Multi-Trial Coordination
Clinical Research Coordinator: Lead Multi-Trial Coordination

IQVIA LLC • Kansas City (MO)

On-site
USD 38,000 - 95,000
Incentives
Health benefits
On-Site Clinical Research Coordinator: Lead Trials
On-Site Clinical Research Coordinator: Lead Trials

IQVIA • Rolla (MO)

On-site
USD 44,000 - 111,000
Clinical Research Coordinator: Multi‑Trial Lead
Clinical Research Coordinator: Multi‑Trial Lead

IQVIA • Mexico (MO)

On-site
USD 44,000 - 111,000
Equal opportunity employer
On-Site Clinical Research Coordinator I — Start Your Trials
On-Site Clinical Research Coordinator I — Start Your Trials

IQVIA Argentina • Elkhorn (WI)

On-site
USD 38,000 - 95,000
Clinical Research Coordinator: Lead Trials & On-site
Clinical Research Coordinator: Lead Trials & On-site

IQVIA • Fulton (MO)

On-site
USD 44,000 - 111,000
Clinical Research Coordinator — Multi‑Trial Specialist
Clinical Research Coordinator — Multi‑Trial Specialist

IQVIA • Columbia Township (MO)

On-site
USD 44,000 - 111,000
Senior Research Coordinator
Senior Research Coordinator

IQVIA LLC • Lexington (KY)

On-site
USD 44,000 - 111,000
Senior CRC: Lead Multi-Trial Coordination On-Site
Senior CRC: Lead Multi-Trial Coordination On-Site

IQVIA Argentina • Rolla (MO)

On-site
USD 44,000 - 111,000
On-Site Senior CRC: Lead Multi‑Trial Clinical Research
On-Site Senior CRC: Lead Multi‑Trial Clinical Research

IQVIA Argentina • Fulton (MO)

On-site
USD 44,000 - 111,000