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IQVIA

Senior Clinical Research Coordinator

IQVIA

. Manage 2–6 clinical trials of varying complexity .

Posted 9/21/2026full-timeJefferson City • Missouri • United StatesSenior💰 $44,300 - $110,500 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in managing clinical trials, including patient recruitment, regulatory documentation, and site operations. Proficient in performing clinical procedures such as phlebotomy and ECGs, with strong communication and mentoring skills.

Highest-signal resume keywords
Clinical Trial ManagementPatient RecruitmentRegulatory DocumentationPhlebotomyECG Conducting

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical ProceduresVital Signs MonitoringLaboratory Specimen ProcessingSite Operations UnderstandingDrug Development Process Knowledge
Soft Skills
Strong Written CommunicationStrong Verbal CommunicationAttention to DetailTime Management
Tools & Technologies
CTMSECRFsMicrosoft Office
Certifications & Qualifications
CRC ICRC II
Industry Keywords
Clinical Research CoordinatorClinical Investigative SiteInformed ConsentSite Audits

About the role

Key responsibilities & impact
  • Manage 2–6 clinical trials of varying complexity
  • Perform clinical procedures
  • Lead study coordination from start to finish
  • Recruit patients and obtain informed consent
  • Maintain regulatory documentation
  • Participate in site audits
  • Work with investigators, sponsors, and monitors
  • Mentor junior staff and contribute to internal training

Requirements

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

Benefits

Comp & perks
  • Professional growth opportunities
  • Exposure to diverse clinical trials and multiple therapeutic areas
  • Collaborative team environment
  • Mentorship and contribution to internal training
  • Health and welfare benefits may be offered
  • Incentive plans, bonuses, and/or other forms of compensation may be offered