Clinical Research Associate Job at ICON, UK | Life Sciences | Apply Online
If you are a life sciences or nursing graduate looking to transition your scientific background into site-level operations with a global industry leader, this full-time position at ICON plc is an outstanding opportunity. Located in Northamptonshire, this office-based role sits within the Clinical Research Site Services division. For organized professionals searching for a high-impact Clinical Research Associate Job or site coordinator pathway, this role provides the structure needed to master protocol compliance, patient tracking, and data auditing. It serves as an excellent launchpad for a long-term Clinical Research Job and stands out as a premier entry-to-mid-level Life Sciences Job.
About The Company
ICON plc is a world-leading global healthcare intelligence and clinical research organization (CRO) dedicated to accelerating the development of medical therapeutics. Through its specialized Full Service & Corporate Support division, ICON partners directly with active clinical sites to optimize data quality, accelerate study timelines, and ensure patient safety. ICON is celebrated globally for fostering an inclusive environment that drives innovation, rewards high performance, and nurtures early-career talent through robust country-specific wellness and professional development frameworks.
Clinical Research Associate Job – Key Responsibilities
As a CRC Associate, you will contribute directly to clinical coordination activities, ensuring high-quality data collection, strict protocol adherence, and patient safety.
Your day-to-day administrative and site coordination duties will include:
- Study Setup & Conduct: Supporting the operational setup, coordination, and day-to-day conduct of clinical trials in accordance with specific protocols, ICH-GCP guidelines, and local regulations.
- Enrollment Support: Assisting with patient pre-screening, informed consent documentation, and active enrollment activities under the direct supervision of senior site staff.
- Data & eCRF Management: Ensuring the accurate, timely completion of raw source documentation and electronic case report forms (eCRFs) to support data quality metrics.
- Trial File Maintenance: Organizing and maintaining study files, essential logs, and Trial Master File (TMF) content to ensure complete site audit-readiness.
- Logistical Scheduling: Coordinating study visit timelines, scheduling patient appointments, and ensuring all required laboratory assessments and clinical procedures are executed per protocol.
- Cross-Functional Collaboration: Collaborating with clinical monitors, principal investigators, and internal teams to resolve active data queries and support continuous quality improvement.
Qualifications & Requirements For Clinical Research Associate Job
This vacancy is specifically tailored for detail-oriented individuals who possess a foundational understanding of clinical trial frameworks and an eagerness to expand their regulatory compliance knowledge.
- Educational Foundation: A Bachelor’s degree in life sciences, nursing, pharmacy, or a related healthcare major is required. Equivalent experience in an active clinical or healthcare setting will also be fully considered.
- Experience Range: Initial experience working within clinical research or a similar highly regulated environment is preferred.
- Regulatory Knowledge: A basic understanding of clinical trial processes, Good Clinical Practice (GCP) guidelines, and regulatory requirements, paired with a strong willingness to learn.
- Core Competencies: Strong organizational skills with the ability to handle multiple tasks, priorities, and deadlines under accuracy parameters, alongside a meticulous attention to detail.
- Communication Style: Effective verbal and written interpersonal communication skills to work collaboratively within a matrixed team ecosystem.
- Logistics: Full-time, office-based position located in Northamptonshire.
In short, the CRC Associate position at ICON is a definitive, office-based route to transitioning your scientific degree or nursing experience into a highly marketable asset within the CRO industry. Securing this role allows you to step away from basic healthcare tasks or isolated laboratory benchwork to master global TMF documentation, GCP data auditing, and site logistics. If you possess an analytical mind, a passion for data quality, and are ready to grow within Northamptonshire, apply today to secure this premier Clinical Research Associate Job.
