Remote Ophthalmology Clinical Research Associate II

Parexel International

United States

Remote

USD 85,000 - 120,000

Full time

12 days ago
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Benefits offered by this job

Health Insurance
Vision Insurance
Dental Insurance
Tuition Reimbursement
Vacation Time
Flexible Spending
Work/Life Balance
401(k) Match
Pet Insurance

Job summary

Parexel is seeking a Clinical Research Associate (CRA) with ophthalmology monitoring experience to join our global clinical research team. You will manage sites, ensure study quality, patient safety, regulatory compliance, and accurate data while guiding sites through monitoring visits.

Responsibilities include site qualification, initiation, monitoring, and closeout visits, building strong site relationships, and supporting enrollment and study delivery across therapeutic areas with a focus on

Qualifications

  • Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline
  • 18+ months of direct onsite monitoring experience as a CRA
  • Ophthalmology clinical trial monitoring experience
  • Knowledge of Good Clinical Practice and regulatory requirements
  • Experience with trial management and document systems
  • Strong interpersonal, written, verbal, organizational, and problem-solving skills

Responsibilities

  • Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned clinical sites
  • Manage site quality and delivery from site identification through closeout
  • Serve as primary contact for assigned sites and resolve issues to support study execution
  • Oversee study integrity and build relationships with investigators and site staff
  • Review trial performance and safeguard rights and safety of participants
  • Develop patient recruitment strategies with sites to support enrollment timelines
  • Ensure compliance with SOPs, protocols, amendments, GCP, and regulatory requirements
  • Evaluate data quality, site performance, and investigational product accountability
  • Monitor regulatory documentation completeness and perform site document verification

Skills

Site relationship management
Communication
Problem solving
Independent work
Client focus
Multitasking
Quality and detail
Team collaboration

Education

Bachelor's degree in biological sciences / health discipline

Tools

CTMS
EDMS
Excel
Word

Job description

Parexel is seeking a Clinical Research Associate (CRA) with ophthalmology monitoring experience to join our global clinical research team. You will manage sites, ensure study quality, patient safety, regulatory compliance, and accurate data while guiding sites through monitoring visits.

Responsibilities include site qualification, initiation, monitoring, and closeout visits, building strong site relationships, and supporting enrollment and study delivery across therapeutic areas with a focus on

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