Clinical Research Coordinator

East Coast Institute For Research; Canton (GA); On-site; USD 55,000 - 70,000; Full time

Job summary

A leading research institute is seeking a Clinical Research Coordinator to oversee daily operations and coordinate clinical studies. This role includes responsibilities such as managing site selection, monitoring recruitment, and ensuring compliance with regulatory standards. Ideal candidates will possess strong interpersonal and organizational skills along with related certifications, collaborating closely with both internal teams and external stakeholders.

Benefits

Paid time off

Flexible schedule

Advancement opportunities

401(k) with company match

Health, dental, and vision insurance

HSA with company match

Life and disability coverage

Employee referral program

Qualifications

• Minimum 2 years of CRC experience required.
• Certification as CCRP or CCRC preferred.
• Sound knowledge of ICH/GCP and regulatory requirements.

Responsibilities

• Manage site selection visits and oversee study startup activities.
• Monitor enrollment efforts and address challenges in recruitment.
• Support study staff through mentoring and guidance.

Skills

Interpersonal skills

Organizational skills

Medical terminology

Confidentiality

Teamwork

Education

High school diploma

Bachelor’s degree in related field

Certification as a CCRP or CCRC

Tools

Microsoft Office

Excel

Job description

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East Coast Institute For Research provided pay range

This range is provided by East Coast Institute For Research. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$55,000.00/yr - $70,000.00/yr

CLINICAL RESEARCH COORDINATOR

PURPOSE

To work as an integral member of the Rovia/Investigator site staff, maintaining the day-to-day operations and assist in the development of the Rovia network. This includes planning, coordinating, and executing clinical studies in accordance with the protocol, contracted scope of work, ICH/GCP, Sponsor, CRO, and Rovia SOPs and any relevant local guidelines and regulations.

Responsibilities

• Manages site selection visits and coordinates study startup activities (e.g., Source Data ID log, recruitment plan, site blinding plan, and temperature log).
• Oversees facility issues in collaboration with the Site Manager and Director, and leads weekly site meetings.
• Manages investigator signature processes and supports study recruitment and contingency planning.
• Monitors and tracks pre-screening, enrollment efforts, and progress toward study enrollment goals, addressing delays or changes promptly.
• Identifies difficult-to-enroll studies and collaborates with the recruitment manager to improve enrollment.
• Ensures timely data entry in EDC and Clinical Conductor platforms and resolves any issues.
• Leads or attends study initiation, interim monitor, and close-out visits.
• Reviews site monitor reports, follows up on action items, and conducts quality checks on subject visits.
• Collaborates with site managers and compliance teams to identify and address quality issues.
• Works with the Source Document Specialist to ensure source documents are ready for patient visits.
• Provides support and guidance to site research staff, including training, troubleshooting, and resource management.
• Acts as a liaison between the site, financial team, and management, and suggests improvements to workflows.
• Develops and maintains investigator relationships, providing regular progress reports.
• Onboards and trains new staff, tracks their progress, and addresses gaps in training.
• Participates in site staff evaluations and new employee interviews.
• Serves as a mentor and fosters a positive work environment.
• Conducts presentations at company training events and collaborates on external relationships for specialized study protocols.
• Supports special projects, business development, team building, and writing SOPs.
• Perform other duties as assigned.
  
  

Required Knowledge, Skills And Abilities

• Sound knowledge of medical terminology.
• Sound knowledge of ICH/GCP and Regulatory requirements.
• Excellent interpersonal and organizational skills.
• Proficient in the use of Microsoft Office and Excel.
• Fluent in spoken and written English.
• Ability to work independently and in a team environment.
• Ability to maintain confidentiality.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
  
  

Minimum Required Education, Experience And Certifications

• High school diploma required, bachelor’s degree in related field of study preferred.
• Certification as a Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) preferred, or within 6 months of role acceptance.
• 2+ years of CRC experience required, preferably working on industry-sponsored trials.
• Experience in clinical research quality and/or regulatory processes preferred.
• License/Certification status with appropriate CEUs, if applicable.
• Cardiopulmonary resuscitation (CPR)
• International Air Transport Association (IATA)
• Good Clinical Practice (GCP)
  
  

Job Type: Full-time

Benefits

• Paid time off
• Flexible schedule
• Advancement opportunities
• 401(k) with company match
• Health, dental, and vision insurance
• HSA with company match
• Life and disability coverage
• Employee referral program
  
  

Schedule

• Day shift
• Monday to Friday, 8:30AM-5:00PM

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

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