Clinical Research Associate — Trials & Compliance

Worklane GmbH; San Diego (CA); On-site; USD 86,000 - 128,000; Full time

Benefits offered by this job

Comprehensive medical

Vision insurance

Dental insurance

Life insurance

AD&D

Job summary

Resmed is seeking a Clinical Research Associate to support planning, coordination, and execution of clinical studies across sites and teams. The role involves EDC monitoring, data review, and generating study documentation to ensure compliant, timely trials.

The ideal candidate has a life sciences degree and at least 2 years in clinical research, with knowledge of ICH/GCP and FDA regulations. The position offers a full-time hybrid work arrangement with growth opportunities.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Experience in clinical research or related area.

Responsibilities

• Support planning, start-up, execution, monitoring, and closeout of single- and multi-site clinical studies.
• Coordinate day-to-day study operations with internal teams, sites, vendors, and CROs.
• Prepare study documents: protocols, amendments, SDMs, CRFs, and reports.
• Track enrollment, retention, and study metrics for leadership updates.

Skills

Strong organizational skills

Analytical skills

Written communication

Verbal communication

Independent with cross-functional work

Education

Bachelor’s degree in life sciences, health sciences, public health, or related field

Tools

Microsoft Office (SharePoint, Word, Excel, PowerPoint, Outlook)

EDC/CTMS systems

Job description

Resmed is seeking a Clinical Research Associate to support planning, coordination, and execution of clinical studies across sites and teams. The role involves EDC monitoring, data review, and generating study documentation to ensure compliant, timely trials.

The ideal candidate has a life sciences degree and at least 2 years in clinical research, with knowledge of ICH/GCP and FDA regulations. The position offers a full-time hybrid work arrangement with growth opportunities.