CRA II: Travel‑Ready Clinical Trials Specialist (Hybrid/Remote)

Avania

New York (NY)

Hybrid

USD 90,000 - 110,000

Full time

48 hours ago
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Benefits offered by this job

Competitive compensation
Annual bonus
Benefits package
Travel opportunities

Job summary

Avania is seeking a Clinical Research Associate II (CRA II) based in PA, MD, or New York to monitor trials, protect patient rights, and ensure data integrity according to GCP/ISO standards. The role requires travel to investigational sites and routine monitoring tasks across regional studies.

The ideal candidate has 2+ years of CRA experience, knowledge of regulatory requirements, and fluent English. Avania offers a competitive package with benefits and opportunities for career growth.

Qualifications

  • Minimum 2+ years of CRA experience.
  • Based in PA, MD or NY to cover regional studies.
  • Experience with medical device or medical technology studies preferred.
  • GCP-ICH-E6, FDA regulations and ISO 14155/13485 knowledge.
  • Fluent English with strong written and spoken communication.

Responsibilities

  • Oversee monitoring activities at investigational sites with travel.
  • Write visit reports per SOPs and GCP, including site visits.
  • Guide investigators and coordinators in conducting trials.
  • Verify SDV and data consistency with source documents.
  • Collaborate with analytics for data reviews and trend identification.
  • Monitor site completion of action items between visits.
  • Prepare for audits and TMF reviews.
  • Review and write informed consent forms.
  • Prepare trial documents for regulatory submissions.

Skills

CRA experience
Regional coverage
Medical device studies
Regulatory knowledge
GCP-ICH compliance
English fluency
Travel-ready
Planning & prioritizing
Data interpretation

Education

B.A./B.S. or equivalent

Job description

Avania is seeking a Clinical Research Associate II (CRA II) based in PA, MD, or New York to monitor trials, protect patient rights, and ensure data integrity according to GCP/ISO standards. The role requires travel to investigational sites and routine monitoring tasks across regional studies.

The ideal candidate has 2+ years of CRA experience, knowledge of regulatory requirements, and fluent English. Avania offers a competitive package with benefits and opportunities for career growth.

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