Senior CRA – Phase I Oncology (Mountain West)

ICON

Center Square (PA)

Remote

USD 90,000 - 120,000

Full time

14 days+

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Job summary

ICON Plc is seeking a Senior Clinical Research Associate for Phase I Oncology to lead monitoring at Mountain West sites. You will oversee site visits, ensure protocol and GCP compliance, and collaborate with cross-functional teams to ensure timely data collection and reporting.

The role requires strong monitoring expertise, regulatory knowledge, and the ability to manage multiple sites while traveling ~30–50%. ICON offers a sponsor-dedicated environment and opportunities for career development.

Qualifications

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 30-50%).

Responsibilities

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Skills

Clinical trial monitoring
Site management
Data integrity
Regulatory knowledge
Communication skills
Travel readiness

Education

Bachelor's degree in a relevant field

Job description

ICON Plc is seeking a Senior Clinical Research Associate for Phase I Oncology to lead monitoring at Mountain West sites. You will oversee site visits, ensure protocol and GCP compliance, and collaborate with cross-functional teams to ensure timely data collection and reporting.

The role requires strong monitoring expertise, regulatory knowledge, and the ability to manage multiple sites while traveling ~30–50%. ICON offers a sponsor-dedicated environment and opportunities for career development.

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