Jobs · Analyst

Principal Clinical Research Associate - Oncology

CareersElite.com · New Year, MT · 3 wk ago
Analyst$110k–$130k/yrFull-time

Remote • Full-time • $110k - $130k / year

About the role

As a Sr. Clinical Research Associate at ICON, you will oversee and manage clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards. Your focus will be on coordinating clinical trial monitoring delivery, resolving issues, and developing team capability.

Responsibilities

  • Lead site management activities, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and regulatory guidelines.
  • Serve as the primary point of contact for clinical sites, addressing site queries, and resolving issues to maintain site engagement and performance.
  • Ensure the integrity of clinical data by conducting thorough source data verification, reviewing site records, and monitoring for protocol deviations.
  • Mentor and provide guidance to CRAs, contributing to their professional development and supporting the consistent application of best practices across studies.
  • Collaborate with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of clinical trials.

Requirements

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO industry, with a proven track record of managing complex clinical trials.
  • In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
  • Strong leadership and mentoring skills, with the ability to manage and motivate CRAs and site staff effectively.
  • Excellent communication, organizational, and problem-solving skills, with a proactive approach to managing site performance and resolving issues.
  • Willingness to travel as required (approximately 60%).

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

  • Competitive base salary and performance-related incentives.
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Learning and development opportunities through structured training and career pathways.

Benefits may vary depending on role and location.

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