Clinical Research Associate - Cross TA

Regulatory Jobs; Georgia; On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Life insurance

Wellbeing programs

Training & development

Employee assistance

Job summary

ICON Strategic Solutions is seeking a Clinical Research Associate to monitor sites across the Georgia region and ensure ICH‑GCP compliance. You will manage site visits, data entry, and patient safety while collaborating with cross-functional teams.

The role requires 2+ years of on-site monitoring experience in pharma/CRO, strong communication, and willingness to travel up to 50% to support Southeast region sites. A Life Sciences degree or RN is acceptable.

Qualifications

• Bachelor's degree in Life Sciences or equivalent; RN accepted
• 2+ years of on-site monitoring experience in pharma/CRO
• Proficiency in ICH-GCP and local regulations
• Experience with CTMS and eTMF systems
• Strong communication and collaboration skills
• Willingness to travel up to 50% for on-site visits across southeast region

Responsibilities

• Serve as the primary contact between sites and sponsor
• Conduct site visits: selection, initiation, routine monitoring and close-out
• Ensure site compliance with ICH-GCP, SOPs and regulations
• Maintain documentation in CTMS and eTMF
• Support site staff training and compliance records
• Monitor patient safety with AE/SAE/PQC reporting
• Support recruitment and retention at the site
• Oversee drug accountability and storage/return/destruction
• Resolve data queries and ensure timely data entry
• Document site progress and escalate risks to the clinical team
• Track site budgets and payments
• Collaborate with CTAs, LTMs, CTMs

Skills

On-site monitoring

ICH-GCP

CTMS

eTMF

Communication

Travel 50%

Education

Bachelor's degree Life Sciences

RN qualification

Tools

CTMS

eTMF

Job description

Clinical Research Associate - Cross Therapeutic Area - Georgia

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

What You Will Be Doing:

• Serve as the primary point of contact between investigational sites and the sponsor
• Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out
• Ensure site compliance with ICH-GCP, SOPs, and regulations
• Maintain up-to-date documentation in CTMS and eTMF systems
• Support and track site staff training and maintain compliance records
• Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting
• Support subject recruitment and retention efforts at the site level
• Oversee drug accountability and ensure proper storage, return, or destruction
• Resolve data queries and drive timely, high-quality data entry
• Document site progress and escalating risks or issues to the clinical team
• Assist in tracking site budgets and ensuring timely site payments (as applicable)
• Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

• A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN
• Eligible to work in United States without visa sponsorship
• A clinical research professional with 2+ years of on‑site monitoring experience in the pharmaceutical or CRO industry
• Experienced monitoring across multiple therapeutic areas
• Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF
• A clear communicator, problem‑solver, and collaborative team player
• Willing and able to travel up to 50% for on‑site monitoring visits across southeast region; preference given to candidates residing in Georgia near major HUB airports to support efficient regional travel

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.