Remote Senior Clinical Research Associate – West Coast

Parexel

Dover (DE)

Remote

USD 85,000 - 110,000

Full time

33 hours ago

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Job summary

Parexel is seeking a Senior Clinical Research Associate to manage investigator sites, monitor trials, and drive close-out activities in alignment with GCP and Sponsor standards. Responsibilities include site activation, monitoring, data queries, and close-out planning across assigned trials.

The role requires at least 2 years of site monitoring experience, fluency in English, travel readiness, and a life sciences degree.

Qualifications

Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
Monitoring Experience: Minimum 2 years relevant experience in clinical research site monitoring.
Must be fluent in English and in the native language(s) of the country they will work in.
Ability to travel 60-80%.
Valid driver’s license and passport required.

Responsibilities

Monitor investigator sites from activation through to database lock, ensuring timelines and quality deliverables.
Serve as primary point of contact for assigned investigator sites and coordinate with SCP to ensure site delivery quality.
Interface with study team, vendors and sites to facilitate information flow.
Provide investigator site development, coaching and training to ensure protocol compliance and patient safeguarding.
Attend investigator meetings as needed and assist with enrollment, recruitment initiatives and site issue resolution.
Conduct onsite or remote/electronic monitoring as required and ensure compliance with SMP and SOPs.