Senior CRA – Orthopedic Medical Devices, Global Trials

ICON Strategic Solutions

Texas

Sur place

USD 90 000 - 120 000

Plein temps

Il y a 2 jours
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Résumé du poste

ICON Strategic Solutions seeks a Senior Clinical Research Associate to lead monitoring of orthopedic device trials across the Midwest/West region. You will ensure trials comply with protocol, GCP, and regulatory requirements, guiding sites and teams to high-quality data and patient safety.

You will travel ~60% to site visits, provide training, manage multi-site responsibilities, and collaborate with cross-functional teams to drive successful trial execution in sponsor-dedicated model.

Qualifications

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field.
  • 3-5 years of CRA monitoring experience in CRO/pharma environments.
  • Strong CRA with experience managing complex protocols.
  • Medical device experience preferred but not required.
  • Orthopedic experience is a plus but not essential.
  • Experience in sports medicine, trauma, or related therapeutic areas would be beneficial.
  • 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 60%)
  • Limited Canadian travel may be required

Responsabilités

  • 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.

Formation

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Description du poste

ICON Strategic Solutions seeks a Senior Clinical Research Associate to lead monitoring of orthopedic device trials across the Midwest/West region. You will ensure trials comply with protocol, GCP, and regulatory requirements, guiding sites and teams to high-quality data and patient safety.

You will travel ~60% to site visits, provide training, manage multi-site responsibilities, and collaborate with cross-functional teams to drive successful trial execution in sponsor-dedicated model.

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