Clinical Research Site Director

ClinLab Solutions Group; Little Rock (AR); On-site; USD 110,000 - 160,000; Full time

Job summary

ClinLab Solutions Group in Little Rock, AR is seeking a full-time Clinical Research Site Director to lead site operations and drive ownership of studies, patients, and the research team.

You will oversee IRB submissions, regulatory compliance, patient consent, data integrity, and collaboration with investigators and sponsors to advance therapy development while maintaining high standards of patient care.

Qualifications

• 5+ years coordinating industry sponsored clinical trials.
• Experience in a site leadership role.
• Experience with IRB approved protocols.
• Clinical skills including consenting, physical assessments, blood draws, medication administration, and ECGs.
• Attention to regulatory compliance and clean data entry.
• Strong communication across research teams, PIs, sponsors and monitors.
• Interest or experience in Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology or Oncology research.
• Ability to manage multiple protocols simultaneously.

Responsibilities

• Take ownership of assigned studies and patients from identification through enrollment and follow up.
• Oversee screening, randomization, and enrollment activities per IRB protocols.
• Perform and assist with direct patient care including consenting and assessments.
• Manage regulatory compliance, IRB submissions, and AE/SAE tracking.
• Maintain clean data entry and eSource material for all studies.
• Serve as primary contact between research team, PIs, sponsors and monitors.
• Ensure efficient study setup, maintenance and protocol adherence.
• Communicate with leadership and coworkers on items needing correction.
• Learn and apply site technology systems to day-to-day operations.

Skills

Clinical trial coordination

Site leadership

IRB protocols

Regulatory compliance

Data entry / eSource

Communication skills

Patient consent

Job description

Little Rock, Arkansas | Full Time | Onsite

We are seeking a full time Clinical Research Site Director to lead site operations for a growing clinical research organization in Little Rock, Arkansas. This role is ideal for a proven site leader with a strong clinical background who wants to take ownership of studies, patients, and a research team. You will play a direct role in advancing new therapy development across a range of therapeutic areas while ensuring the highest standards of patient care and regulatory compliance.

Responsibilities

• Take ownership of assigned studies and patients from identification through enrollment and follow up.
• Oversee screening, randomization, and enrollment activities in accordance with IRB approved protocols.
• Perform and assist with direct patient care activities including consenting, physical assessments, blood draws, medication administration, and ECGs.
• Manage regulatory compliance, IRB submissions and responses, audit findings, and AE and SAE tracking.
• Maintain clean data entry and eSource material for all assigned studies.
• Serve as the primary communication link between the research team, principal investigators, sponsors, and monitors.
• Ensure efficient study set up, maintenance, and strict protocol adherence across the site.
• Communicate promptly with leadership and coworkers on questions or items needing correction.
• Learn and apply site technology systems to support day to day operations.

Requirements

• 5 plus years of experience coordinating industry sponsored clinical trials.
• Prior experience in a site leadership role.
• Skilled in all aspects of conducting an IRB approved clinical trial protocol.
• Strong clinical skills including consenting, physical assessments, blood draws, medication administration, and ECG.
• Excellent attention to detail for regulatory compliance and clean data entry.
• Strong communication skills with the ability to build relationships across research teams, PIs, sponsors, and monitors.
• Interest or experience in Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, or Oncology research.
• Ability to manage multiple protocols at once while staying organized and focused.