Oncology Clinical Research Associate Lead

6 days ago


Phoenix, Arizona, United States ICON Strategic Solutions Full time
About ICON Strategic Solutions

At ICON, our mission is to help pharmaceutical and biotech companies develop life-changing medicines. We're a global leader in clinical research, with a team of experts dedicated to delivering high-quality services that meet the needs of our clients.

Job Summary

We are seeking an experienced Oncology Clinical Research Associate (CRA) to join our team in Arizona. As a CRA, you will be responsible for ensuring the integrity and quality of clinical trials, working closely with investigators and site staff to ensure compliance with regulatory requirements and good clinical practices.

Key Responsibilities
  • Monitor and manage multiple oncology trials, focusing on quality of life outcomes and regional travel opportunities.
  • Provide leadership and mentoring to junior team members, developing their skills and knowledge to improve trial performance.
  • Act as lead site monitor, training other site monitors on study protocols and procedures.
  • Develop and implement site startup documents, including study initiation visit agendas.
  • Review and provide input on study documents, such as monitoring guidelines.
  • Represent ICON at local and regional meetings, providing updates on trial progress and addressing site concerns.
  • Take over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial.
  • Support country budget development and contract negotiation, collaborating with CCS colleagues.
Requirements
  • Bachelor's degree or equivalent in Biological Sciences, Nursing, or related field.
  • Minimum 2 years' experience in monitoring pharmaceutical industry clinical trials.
  • 1-3 years' experience monitoring Oncology trials.
  • Knowledge of therapeutic areas, with oncology an asset but not required.
  • Analytical/risk-based monitoring experience an asset.
  • Ability to drive patient recruitment strategies and partner with investigators and site staff.
  • Strong communication and influencing skills, with ability to work independently and as part of a team.
  • In-depth knowledge of Good Clinical Practice, ICH guidelines, and local regulatory requirements.
  • Travel up to 50% required.
What ICON Can Offer You

We offer a competitive salary and benefits package, including:

  • Annual leave entitlements.
  • Range of health insurance options.
  • Competitive retirement planning offerings.
  • Global Employee Assistance Programme.
  • Life assurance.
  • Flexible optional benefits, including childcare vouchers, bike purchase schemes, and discounted gym memberships.

Estimated Salary: $80,000 - $110,000 per year, depending on experience.



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