Clinical Research Associate - Ireland

About IQVIA

IQVIA is a premier human data science organization dedicated to delivering superior insights and innovative solutions in healthcare to improve patient outcomes. Established from the merger of IMS Health and Quintiles, IQVIA combines healthcare data expertise, domain knowledge, cutting-edge technology, and advanced analytics to push clinical development forward.

Clinical FSP Business Model

IQVIA's clinical Functional Service Provider (FSP) team works exclusively with a single sponsor partner ensuring high-quality delivery through collaboration and in-person interactions during study start-up and execution. The clinical teams are valued for their expertise and given ongoing development opportunities, including thorough onboarding, daily problem-solving, and dedicated training. Our CRAs develop deep indication and molecule knowledge as they align with sponsor SOPs, fostering continuity and specialization.

Role Overview

• Function as the primary clinical research associate partner to one or two protocols, typically in areas such as Oncology, Neurology, Immunology, or Diabetes.
• Perform site management and monitoring across Ireland, being on-site around 6-8 days per month depending on sponsor needs.
• Work under a dedicated IQVIA line manager with a permanent employment contract.
• Experience balanced workloads with reduced travel requirements (~30% or less) through Fit for Purpose Monitoring methods integrating remote monitoring.
• Enjoy a supportive work-life balance and opportunities to advance career development while contributing to cutting-edge therapeutic development.

Key Responsibilities

• Manage and monitor clinical trial sites throughout the country.
• Collaborate with sites to implement and track recruitment strategies.
• Conduct protocol and study-related training for assigned sites.
• Compile and update monitoring visit reports and associated action plans.
• Provide co-monitoring, training, and mentorship to junior clinical research associates when appropriate.

Candidate Requirements

• Possess a Life Sciences degree or equivalent nursing experience.
• Hold a minimum of 12 months of experience in independent on-site clinical monitoring.
• Proven ability to handle multiple protocols involving diverse drug indications with effective time management.
• Demonstrate comprehensive knowledge of Good Clinical Practice (GCP) guidelines.
• Be flexible and willing to travel nationwide.
• Maintain a valid full driving license.
• Exhibit excellent communication, writing, and presentation skills; fluency in English is mandatory.
• This position is not open to visa sponsorship applicants.

Additional Information

IQVIA does not sponsor visas for this role. Candidates are expected to provide truthful and complete information during the recruitment process. Any misrepresentations may lead to disqualification or employment termination in line with legal guidelines.

What We Offer

• Competitive salary with comprehensive benefits package.
• Car allowance provided.
• Commitment to team stability and consistent workloads.
• Opportunities for genuine career progression and development.
• Involvement in development of innovative medicines at the forefront of healthcare.