Regional CRA II: Early Development, Multi-Therapeutic

ICON Strategic Solutions; Missouri; On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Life insurance

Wellbeing resources

Career development

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate for Early Development with a multi-therapeutic focus. The role involves close collaboration with sponsor teams, site visits, and ensuring compliance across ICH-GCP standards.

The ideal candidate has 2+ years of on-site monitoring, a Life Sciences degree or RN, and willingness to travel up to 60% to major hub clinics. This position supports diverse early-phase studies and cross-functional partnership.

Qualifications

• Bachelor's degree in Life Sciences or RN required.
• 2+ years on-site monitoring in pharmaceutical or CRO environment.
• Willing to travel up to 60% to meet on-site monitoring expectations.

Responsibilities

• Serve as the primary point of contact between investigation sites and sponsor for early development multi-therapeutic trials.
• Conduct site visits including site selection, initiation, routine monitoring, and close-out.
• Ensure site compliance with ICH-GCP, SOPs, and local regulations.
• Maintain up-to-date documentation in CTMS and eTMF.
• Support and track site staff training and maintain compliance records.
• Monitor patient safety with timely AE/SAE/PQC reporting.
• Support recruitment and retention efforts at the site level.
• Oversee drug accountability and proper storage/destruction.
• Collaborate with cross-functional partners including CTAs, LTMs, and CTMs.

Skills

Independent monitoring experience

Phase I/II experience

Multiple therapeutic areas

Willing to travel 60%

US-based near hubs

Education

Bachelor's degree in Life Sciences or RN

Tools

CTMS

eTMF

Job description

ICON Strategic Solutions is seeking a Clinical Research Associate for Early Development with a multi-therapeutic focus. The role involves close collaboration with sponsor teams, site visits, and ensuring compliance across ICH-GCP standards.

The ideal candidate has 2+ years of on-site monitoring, a Life Sciences degree or RN, and willingness to travel up to 60% to major hub clinics. This position supports diverse early-phase studies and cross-functional partnership.