Clinical Research Associate I - Onsite Trials & Compliance

CND Life Sciences, Inc.; Scottsdale (AZ); On-site; USD 85,000 - 115,000; Full time

Job summary

CND Life Sciences, Inc. is seeking a Clinical Research Associate to oversee and monitor trials at the CND Clinical Research Center and investigator sites.

The CRA ensures studies follow protocols, ICH-GCP, SOPs, and timelines while collaborating with investigators and cross-functional teams to maintain high standards. Responsibilities include site initiation, monitoring, subject recruitment, regulatory submissions, data integrity, safety reporting, and timely communication.

Qualifications

• Minimum of 5 years of clinical research experience as a Clinical Research Coordinator or at least 2 years as a Clinical Research Associate.
• Neurology experience preferred.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trial conduct.
• Experience with Phase I–III trials; NIH/government protocols a plus.

Responsibilities

• Ensure trials comply with study protocols, ICH-GCP guidelines, relevant regulations and SOPs.
• Assist with subject recruitment, informed consent, site visits, and regulatory start-up activities.
• Conduct site initiation visits and monitoring per plans; manage data entry, queries, and safety reporting.
• Maintain proactive site communication and documentation; oversee budget-related invoicing and milestones.
• Support collaboration with internal/external teams and vendors to meet milestones and budgets.

Skills

Clinical research

Neurology experience

GCP/regulatory knowledge

IT tools (EDC/CTMS/MS365)

Communication skills

Multitasking/attention to detail

Team collaboration

Travel willingness

Education

Bachelor's degree (BS)

CITI GCP certification

Tools

MS 365

EDC systems

CTMS

Job description

CND Life Sciences, Inc. is seeking a Clinical Research Associate to oversee and monitor trials at the CND Clinical Research Center and investigator sites.

The CRA ensures studies follow protocols, ICH-GCP, SOPs, and timelines while collaborating with investigators and cross-functional teams to maintain high standards. Responsibilities include site initiation, monitoring, subject recruitment, regulatory submissions, data integrity, safety reporting, and timely communication.