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Premier Research International

Contract research organization for clinical development

Clinical Research Associate 2

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in PolandPLN143k /yr

About the Job

Requirements

  • An undergraduate degree or its international equivalent in a clinical, science, or health-related field from an accredited institution, a licensed health-care professional such as a registered nurse, or equivalent work experience is required.
  • Previous clinical research experience, including at least one year of independent monitoring, is required.
  • Experience supporting Phase II and III studies is required.

Responsibilities

  • Deliver quality, timely monitoring reports for sponsor approval within Clinical Monitoring Plan timelines.
  • Submit expenses according to travel and expense requirements and company guidelines.
  • Monitor remotely, onsite, or by another approved mode, focusing on data integrity and patient safety in accordance with country-specific regulations.
  • Plan day-to-day clinical study monitoring activities and set priorities for each site.
  • Prepare for and conduct onsite qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by the clinical monitoring plan.
  • Maintain the Trial Master File (TMF) or electronic Trial Master File (eTMF) according to organizational processes and filing guidelines.
  • Understand the essential documents required under ICH/GCP Section 8.
  • Review site documents and verify that they are accurate, complete, current, and include required updates.

Desired Qualifications

  • Experience working across all or some of the following therapy areas: Neurology, Oncology, and Dermatology.

About the Company

Premier Research International

Contract research organization for clinical development

Premier Research provides specialized clinical development services for biotech and specialty pharma, focusing on the therapeutic areas where leading scientists work. It supports end-to-end clinical trials including design, site management, data management, biostatistics, regulatory affairs, and medical writing across 20+ countries with about 1,500 employees. It differentiates itself with deep expertise in select therapeutic areas, strong execution, global reach, close collaboration, patient impact, and flexible working conditions. Its goal is to help biotech and pharma teams bring safe, effective therapies to patients faster through high-quality development and regulatory support.

Company size
1,001-5,000
Company stage
Acquired
Total funding
$79.2M
Headquarters
Morrisville, NC
Founded
1989

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