Senior Clinical Research Associate, Early Clinical Development

IQVIA

Carlsbad, CAFull-timePosted Apr 20, 2026

Behavioral Health Market Context

Latest national behavioral health workforce report (2026-W22)California behavioral health workforce newsBrowse all behavioral health workforce news
Apply Nowvia Indeed

Benefits

The potential base pay range for this role, when annualized, is $87,200.00 - $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

  • •Bachelor’s degree in life sciences or health-related field (or equivalent experience)
  • •Requires at least 1.5 years of on-site monitoring experience
  • •Strong understanding of GCP, ICH guidelines, and regulatory requirements
  • •Ability to travel as required by the project
  • •1 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)
Apply for this Position

More Jobs