Clinical Research Coordinator I/II/III

Jobtailor; Little Rock (AR); On-site; USD 52,000 - 78,000; Full time

Job summary

Jobtailor is seeking a detail-oriented Clinical Research Coordinator to facilitate and coordinate daily activities across multiple studies, working with investigators, sponsors, and site staff.

Responsibilities include participant recruitment, consent, data entry, study timelines, and ensuring compliance with CFR and human research conduct; travel across Arkansas is required.

Qualifications

• Cons academic coursework or experience in clinical research coordination.
• Familiarity with CFRs and human research protections.
• Proven ability to plan, coordinate and manage data collection activities.

Responsibilities

• Coordinate daily clinical research activities across multiple studies.
• Recruit and screen participants and obtain informed consent.
• Maintain study data, timelines and reports; ensure regulatory compliance.

Skills

Clinical Research Experience

Study Coordination

Data Collection

Effective Communication

Education

Bachelor's degree

CCRP Certification

CCRC Certification

Tools

Research Software

Project Databases

Job description

• Facilitate and coordinate daily clinical research activities for multiple research studies
• Work closely with investigators, research sponsors, contract research organization representatives, research staff, and UAMS institutional oversight offices
• Recruit and screen participants
• Obtain consent and conduct enrollment
• Coordinate study visits, appointments, and reminder calls
• Collect surveys and biometrics
• Organize data collection events and ensure study supplies are ordered
• Deliver and/or transport study-related items to eligible participants as needed
• Maintain project/research databases and enter data accurately
• Maintain study files and generate reports
• Develop and maintain study timelines
• Follow standard operating procedures and recommend quality improvements
• Adhere to federal regulations and human research conduct requirements
• Support regional study sites across Arkansas, requiring travel
• Foster relationships with patients, participants, families, study personnel, collaborators, and community organizations
• Co-facilitate workshops and conduct outreach and community-based recruitment
• Participate in staff and organizational meetings
• Perform other duties as assigned

Requirements

• Level I: Bachelor's degree plus three (3) years of general research experience, or High School diploma/GED plus seven (7) years of general research experience required
• Level II: Bachelor's degree plus three (3) years of clinical research experience with demonstrated proficiency in study planning/development, study coordination/management, and/or data collection required
• Level III: Bachelor's degree plus three (3) years of clinical research experience with demonstrated proficiency in study planning/development, study coordination/management, and/or data collection required
• Level III: CCRP, CCRC, or equivalent professional certification required at hire
• Obtain CRS Certification within 2 years of hire
• Proof of legal authority to work in the United States on the first day of employment
• Pre-employment screening, including criminal background, drug testing, and/or education verification
• Ability to organize complex projects and provide attention to detail
• Effective communication skills
• Working knowledge of the Code of Federal Regulations and the Code of Conduct for human research
• Ability to travel to regional study sites across the state
• Ability to perform the stated physical activities, including sitting, standing, talking, keyboarding, driving, and walking

Core Competencies

Demonstrates expertise in clinical research coordination, including participant recruitment, data collection, and adherence to federal regulations. Proficient in managing study timelines and maintaining accurate project databases while fostering relationships with diverse stakeholders.

Highest-signal resume keywords

• Clinical Research Experience
• Study Coordination/Management
• Data Collection
• CCRP Certification
• Effective Communication Skills

ATS Optimization Keywords

Hard Skills

• Study Planning/Development
• Data Entry
• Project Management
• Survey Collection
• Biometric Data Collection

Soft Skills

• Attention to Detail
• Organizational Skills
• Relationship Building

Certifications & Qualifications

• CCRP
• CCRC
• CRS Certification

Industry Keywords

• Clinical Research
• Federal Regulations
• Human Research Conduct
• Participant Recruitment
• Community Outreach

Tools & Technologies

• Project Databases
• Research Software