Senior Alzheimer's Clinical Research Associate (Remote)

PPG US ProPharma Group, LLC; San Diego (CA); Remote; USD 90,000 - 120,000; Full time

Benefits offered by this job

Remote work

Job summary

ProPharma is seeking an experienced Clinical Research Associate to monitor and co-monitor sites for ongoing clinical trials, including Alzheimer’s studies, across in-person and remote settings.

The role requires strong communication, regulatory knowledge, and proficiency with EDC/CTMS/eTMF. You will support site startup, training, and data integrity while ensuring compliance with ICH/GCP guidelines.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.
• 5+ years of experience as a Clinical Research Associate.
• 3+ years of experience monitoring Alzheimer's studies.
• Experience with site visits, monitoring reports, and regulatory compliance.

Responsibilities

• Conduct monitoring and co-monitoring visits for assigned sites, in person and remote.
• Prepare and review monitoring reports per SOPs and regulations.
• Support startup activities, site identification and essential documents as needed.
• Train site personnel on protocol requirements and data collection.

Skills

Communication

MS Office

EDC

CTMS

IVRS

eTMF

GCP/ICH guidelines

Regulatory knowledge

Prioritize & plan

Education

Bachelor's degree or equivalent

Tools

EDC

CTMS

IVRS

eTMF

Job description

ProPharma is seeking an experienced Clinical Research Associate to monitor and co-monitor sites for ongoing clinical trials, including Alzheimer’s studies, across in-person and remote settings.

The role requires strong communication, regulatory knowledge, and proficiency with EDC/CTMS/eTMF. You will support site startup, training, and data integrity while ensuring compliance with ICH/GCP guidelines.