Senior Research Coordinator

IQVIA

Senior Research Coordinator managing 2–6 clinical trials while collaborating with investigators and mentoring junior staff. Avacare provides a dynamic environment in clinical research.

Posted 7/23/2026full-timeLexington • Kentucky • 🇺🇸 United StatesSenior💰 $44,300 - $110,500 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trials, including obtaining vital signs, performing phlebotomy, and conducting ECGs. Proficient in site operations and the drug development process, with strong communication and time management skills.

Highest-signal resume keywords

Clinical Research CoordinationPhlebotomyECG ConductingCTMS UsageECRF Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Vital Signs AcquisitionLab Specimen ProcessingClinical Trial ManagementDrug Development ProcessClinical Research Experience

Soft Skills

Written CommunicationVerbal CommunicationAttention to DetailTime ManagementAdaptability

Tools & Technologies

CTMSECRFsMicrosoft Office

Industry Keywords

Clinical ResearchInvestigative SiteStudy CoordinationTrial ManagementContinuous Learning

About the role

Key responsibilities & impact

Manage 2–6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
Work closely with investigators, sponsors, and monitors while mentoring junior staff and contributing to internal training.
Be part of a supportive team that values initiative, adaptability, and continuous learning.
Experience the synergy of working within a local SMO backed by the resources and reach of a global CRO.

Requirements

What you’ll need

Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
Solid understanding of site operations and the drug development process.
CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.
CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
Strong written and verbal communication skills, with attention to detail and time management.
Comfortable using CTMS, eCRFs, and Microsoft Office tools.

Benefits

Comp & perks

health insurance
retirement plans
paid time off
flexible work arrangements
professional development