Clinical Research Associate, IQVIA Biotech

IQVIA

Ithaca, NYFull-time

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Benefits

The potential base pay range for this role, when annualized, is $71,900.00 - $169,300.00The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time)Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits

Qualifications

  • •IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates with a minimum of 6 months on-site monitoring experience
  • •Must have experience monitoring in oncology solid tumor
  • •Bachelor’s degree in life sciences or health-related field (or equivalent experience)
  • •Requires at least 1 year of on-site monitoring experience
  • •Strong understanding of GCP, ICH guidelines, and regulatory requirements
  • •Ability to travel as required by the project
  • •3 more items(s)

Responsibilities

  • •We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials
  • •In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations
  • •Your work will directly contribute to the integrity and quality of clinical research data
  • •Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines
  • •Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals
  • •Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues
  • •Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity
  • •Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries
  • •Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards
  • •Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence
  • •Work closely with cross-functional project teams to support study execution and ensure alignment with project goals
  • •Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking
  • •9 more items(s)
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