Clinical Study Associate Role at ICON Strategic Solutions US
ICON Strategic Solutions is hiring a Clinical Study Associate for a remote clinical research job within its Global Clinical Development Operations. This role offers an excellent opportunity for professionals seeking to grow their career as a clinical study associate while supporting global clinical trials for a dedicated pharmaceutical sponsor.
Job Details:
- Job Role: Clinical Study Associate
- Job ID: JR141448
- Location: Remote
- Department: Clinical Operations
- Company: ICON Strategic Solutions
- Employment Type: Full-time
- Industry: Clinical Research / Pharmaceutical
About the Company:
ICON plc is a world-leading healthcare intelligence and clinical research organization. ICON Strategic Solutions partners with pharmaceutical and biotechnology companies to deliver high-quality clinical research services. The company is committed to innovation, regulatory excellence, and fostering an inclusive work culture that supports professional growth and global impact. Explore more remote job offers at ICON.
Educational Requirements for Clinical Study Associate Role:
- Bachelor’s degree in Life Sciences, Health Sciences, or a related discipline
- Candidates with relevant clinical research experience will be preferred
Key Responsibilities for Clinical Study Associate Role:
- Support day-to-day clinical study activities under the supervision of the CSA Manager
- Assist in planning and execution of global clinical studies
- Ensure regulatory inspection readiness and protocol compliance
- Collaborate with clinical study teams and Clinical Research Organizations (CROs)
- Maintain study documentation, rosters, and training matrices
- Support TMF quality control activities
- Track vendor budgets, invoices, and study metrics
- Monitor site reports and escalate concerns to the Clinical Study Manager
Skills Required for Clinical Study Associate Role:
- Experience working in a clinical research job or related role
- Knowledge of Veeva Vault (CDMS and CTMS)
- Understanding of global regulatory and compliance requirements
- Strong organizational and task management skills
- Excellent communication and teamwork abilities
- Ability to work independently with minimal supervision
- Proficiency in business English (written and verbal)
Benefits of the Clinical Study Associate Role:
- Competitive salary package
- Remote work flexibility
- Comprehensive health insurance plans
- Retirement planning benefits
- Annual leave entitlements
- Global Employee Assistance Programme
- Life assurance and wellness benefits
- Inclusive and supportive work environment
