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About the Role
As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This is a sponsor dedicated position supporting various TA areas.
Responsibilities
- Contribute to clinical trial monitoring activities, taking responsibility for deliverables and working collaboratively.
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
Requirements
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 1 year of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to travel as required (approximately 60%).
- Must be located in PA, NY, NJ, MA, ME, VT, NH, CT, RI.
- Must have the legal right to work in the country where the role is based.
Skills
- Clinical trial monitoring
- Protocol compliance
- Data integrity
- Patient safety
- Data review
- Query resolution
- Study documentation
- Organizational skills
- Communication skills
- Attention to detail
Location
- NY
- NJ
- PA
- MA
- ME
- VT
- NH
- CT
- RI
Work Type
- Full-time
- Hybrid
Experience Level
- Minimum of 1 year of experience as a Clinical Research Associate
Education Level
- Bachelor's degree in a scientific or healthcare-related field
Salary/Compensations
- $91,336.00-$114,170.00
Benefits
- 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
About the Company
- 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.
Equal Opportunity
- 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.