Senior Research Coordinator

Jobtailor; Lexington (KY); On-site; USD 52,000 - 76,000; Full time

Job summary

Jobtailor in Lexington, KY seeks a Clinical Research Coordinator to manage trials from initiation to closeout, coordinate study activities, and ensure regulatory compliance. The role requires direct collaboration with investigators, sponsors, and monitors.

Ideal candidates will bring hands-on phlebotomy, ECG, vitals collection, and strong communication skills. Knowledge of CTMS and ECRFs is essential, with a focus on timely documentation and data integrity.

Qualifications

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

Responsibilities

• 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.

Skills

Clinical Research Coordination

Phlebotomy

ECG Conducting

CTMS Usage

ECRF Management

Tools

CTMS

ECRFs

Microsoft Office

Job description

• 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

• 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.

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 Coordination
• Phlebotomy
• ECG Conducting
• CTMS Usage
• ECRF Management

ATS Optimization Keywords

Hard Skills

• Vital Signs Acquisition
• Lab Specimen Processing
• Clinical Trial Management
• Drug Development Process
• Clinical Research Experience

Soft Skills

• Written Communication
• Verbal Communication
• Attention to Detail
• Time Management
• Adaptability

Industry Keywords

• Clinical Research
• Investigative Site
• Study Coordination
• Trial Management
• Continuous Learning

Tools & Technologies

• CTMS
• ECRFs
• Microsoft Office