Remote Clinical Research Associate - US Trials, OA Focus

NBCD

Town of Texas (WI)

On-site

USD 70,000 - 95,000

Full time

14 days+
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Job summary

NBCD is a US-based CRO seeking a Clinical Research Associate to monitor trials and ensure patient safety, data integrity, and regulatory compliance across sites. You will conduct feasibility, site initiation, monitoring and close-out visits, while collaborating with Investigators and Study Coordinators; remote/home-based role with travel up to 75%.

The role offers exposure to global studies, provides opportunities to influence protocol design, and requires independent work with supportive

Qualifications

  • Bachelor’s degree in biology, pharmacy, nursing or other health care related discipline.
  • 2+ years of CRA experience with monitoring and site management activities.
  • Knowledge of ICH-GCP, regulatory requirements and trial methodology.
  • Strong interpersonal, written and verbal communication skills.
  • Experience working independently with support from senior team members.

Responsibilities

  • Conduct feasibility visits, site initiation visits, monitoring visits and close-out visits at assigned sites and generate visit reports.
  • Ensure study quality on site through Source Data Verification/Review and drug accountability.
  • Protect patients by safeguarding rights and well-being of subjects.
  • Build relationships with Investigators and Coordinators to enable smooth collaboration.
  • Develop recruitment strategies with sites to meet enrollment timelines and ensure SOPs/regulatory compliance.

Skills

CRA experience (2+ years)
ICH-GCP knowledge
Clinical trial monitoring
Remote work experience

Education

Bachelor’s degree in biology, pharmacy, nursing or other health care related discipline.

Job description

NBCD is a US-based CRO seeking a Clinical Research Associate to monitor trials and ensure patient safety, data integrity, and regulatory compliance across sites. You will conduct feasibility, site initiation, monitoring and close-out visits, while collaborating with Investigators and Study Coordinators; remote/home-based role with travel up to 75%.

The role offers exposure to global studies, provides opportunities to influence protocol design, and requires independent work with supportive

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