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Senior CRA

ICON plc
Posted a month ago, valid for 15 days
Location

Los Angeles, CA 90053, US

Salary

$115,000 - $138,000 per year

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Contract type

Full Time

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Sonic Summary

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  • ICON Plc is seeking a Senior Clinical Research Associate (CRA) to oversee and manage clinical trial activities.
  • The role requires an advanced degree in a relevant field and five years of experience as a Clinical Research Associate, particularly with oncology monitoring.
  • Responsibilities include monitoring clinical trial sites, conducting site visits, and collaborating with cross-functional teams to ensure compliance and data integrity.
  • The position demands excellent communication and organizational skills, as well as the ability to travel at least 60% of the time.
  • Salary details are not specified in the job description.

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

  • 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.

Your Profile:

  • Advanced degree in a relevant field such as life sciences, nursing, or medicine.
  • 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.
  • Ideal location - Greater Los Angeles area
  • Five years of CRA experience with oncology monitoring experience  
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Are you a current ICON Employee? Please click here to apply: link




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