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Clinical Research Coordinator II

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Solomon Page

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Location:
United States , Nashua

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Category:
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Contract Type:
Employment contract

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Salary:

60000.00 - 75000.00 USD / Year
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Job Description:

We are seeking a motivated and experienced Clinical Research Coordinator II to support industry-sponsored, interventional clinical trials across multiple sites. This is a hands-on role requiring strong patient interaction, operational expertise, and the ability to manage studies from start-up through close-out in a fast-paced environment.

Job Responsibility:

  • Coordinate day-to-day clinical trial activities across multiple therapeutic areas, including ophthalmology, dermatology, and pulmonology
  • Support studies at headquarters and satellite site locations
  • Conduct patient-facing activities, including informed consent, visit scheduling, and follow-up
  • Manage patient recruitment and enrollment through database reviews, outreach, pre-screening, and ongoing communication
  • Perform blood draws and manage biospecimen processing and shipping per protocol
  • Maintain accurate study documentation, source data, and regulatory binders across CTMS, EDC, and other systems
  • Support monitoring visits and participate in internal and external audits
  • Serve as a key liaison between sponsors, CROs, investigators, and internal teams
  • Provide cross-functional support as needed to meet study timelines and goals

Requirements:

  • Minimum of 3 years of direct patient-facing clinical research experience in industry-sponsored, interventional drug trials
  • Ophthalmology experience (Technician or Ophthalmology CRC background)
  • Strong patient communication skills with the ability to build trust and support retention
  • Experience with patient care, recruitment, lab specimen handling, monitoring, and audits
  • Excellent organizational, multitasking, and time management skills
  • Willingness and ability to travel regularly (up to 50%) and on site when not traveling

Nice to have:

  • Phlebotomy license or willingness to complete training and obtain licensure
  • Spanish fluency (spoken and written)
  • Experience supporting multi-site or decentralized clinical trials
  • Familiarity with CTMS and electronic regulatory systems
  • Flexible, proactive, and team-oriented with comfort in a high-accountability environment
What we offer:
  • medical
  • dental
  • 401(k)
  • direct deposit
  • commuter benefits

Additional Information:

Job Posted:
January 10, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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