Senior Clinical Research Associate, Early Clinical Development

IQVIA · Carlsbad, CA +2 more

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Clinical OperationsFull-time$90k–$150kCompany career page

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Role summary

IQVIA Biotech seeks a Clinical Research Associate 2 to monitor clinical trial sites and ensure protocol compliance, regulatory adherence, and data integrity. The role involves site management across multiple visit types, staff training, enrollment tracking, and regulatory documentation in early-phase studies.

What they're looking for

Bachelor's degree in life sciences or health-related field
Minimum 1.5 years of onsite monitoring experience
Strong knowledge of GCP, ICH guidelines, and regulatory requirements
Ability to travel as required by assigned projects
Early phase clinical development experience preferred

What you'll be doing

Conduct site selection, initiation, monitoring, and close-out visits aligned with GCP and ICH guidelines
Collaborate with site staff on subject recruitment strategies to meet enrollment timelines and goals
Provide protocol training to site personnel and maintain ongoing communication
Monitor protocol adherence, escalate quality concerns, and track regulatory submissions and data query resolution
Maintain Trial Master Files and Investigator Site Files with essential regulatory documents

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Date posted27 days ago

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