Clinical Associate Job Opportunity at ICON | Apply Now
Clinical associate job opportunities are highly sought after by professionals looking to build a career in clinical research. ICON plc is currently hiring a Clinical Site Associate in Reading, UK. This exciting life sciences job offers the opportunity to work with a leading clinical research organization, support clinical trial activities, and gain valuable experience that can lead to future CRA roles. If you are searching for ICON careers or a rewarding job in UK, this position could be an excellent next step.
- Job Position: Clinical Site Associate
- Company Name: ICON plc
- Job ID: JR144805
- Location: Reading, United Kingdom
About the Company
Clinical associate job seekers exploring ICON careers will find excellent opportunities at ICON plc. ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to advancing clinical development through innovation, quality, and excellence. The company fosters an inclusive environment that supports professional growth, collaboration, and career progression across global clinical research operations.
Clinical Associate Job Description
Clinical associate job professionals joining ICON as a Clinical Site Associate will play a key role in supporting site management activities and ensuring that clinical trials are conducted efficiently, compliantly, and according to high-quality standards. The role involves close collaboration with Clinical Research Associates (CRAs), site staff, and cross-functional teams to support study start-up, maintenance, and close-out activities. This role is office based in Reading (Green Park) with a hybrid working arrangement.
Qualifications
Clinical associate job candidates should possess the following qualifications and skills:
- Bachelor’s degree in Life Sciences, Healthcare, Medical Sciences, or a related field, or equivalent experience.
- Initial experience in clinical research, clinical administration, or a similar regulated environment is highly desirable.
- Strong organizational skills with the ability to manage multiple tasks, priorities, and deadlines.
- High attention to detail and accuracy in documentation and data entry.
- Effective written and verbal communication skills with a customer-focused approach.
- Proficiency in Microsoft Office and comfort working with electronic systems and databases.
- Ability to work collaboratively in a team environment and adapt to changing priorities.
- Ability to commute easily to Reading, UK.
Clinical Associate Job – Key Responsibilities
Clinical associate role responsibilities at ICON include supporting clinical trial site operations and maintaining compliance throughout study activities.
- Supporting site activation activities, including the collection, review, and tracking of essential documents and approvals.
- Maintaining up-to-date site information and status in clinical trial management systems and trackers.
- Assisting CRAs and project teams with site communications, follow-up, and resolution of site-level queries.
- Coordinating logistics for site visits and meetings, including scheduling, documentation preparation, and follow-up actions.
- Ensuring accurate filing and maintenance of essential documents to support inspection and audit readiness.
- Collaborating with internal stakeholders to support timely site payment processing and issue resolution.
- Contributing to process improvement initiatives and sharing best practices to enhance site support efficiency.
Why Join ICON?
Clinical associate job opportunities through ICON careers provide exposure to global clinical research projects, professional development, and a supportive workplace culture. As a leading employer in the clinical research sector, ICON offers employees the chance to contribute to innovative healthcare solutions while building rewarding careers in the industry.
