Clinical Research Associate Job at IQVIA, Ireland | Life Sciences | Apply Now
If you are an experienced clinical operations professional, an oncology monitor, or a qualified nursing specialist looking to anchor your career with a premier global healthcare intelligence leader, this full-time role at IQVIA is an exceptional opportunity. Located out of Dublin, Ireland, this field-based position places you on the frontline of clinical trial delivery and localized data integrity. For detail-oriented monitoring experts searching for a high-value Clinical Research Associate Job, this position within IQVIA’s Functional Service Provider (FSP) division offers single-sponsor alignment, protecting your work-life balance through a highly optimized travel framework. It serves as an elite launchpad to advance a long-term IQVIA Career and stands out as a premier choice for professionals tracking a competitive Life Sciences Job within Europe’s clinical research sector.
- Job Position: Clinical Research Associate – Ireland
- Location: Dublin, Ireland
- Job ID: R1555258
About The Company
IQVIA is a leading global human data science powerhouse and healthcare intelligence organization focused on helping life sciences clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad suite of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive clinical development forward worldwide. This position operates within IQVIA’s Clinical FSP Business Unit. Unlike standard multi-sponsor CRO models, our FSP teams are dedicated exclusively to a single-sponsor pharmaceutical partner. This unique structural framework ensures that you work directly with the sponsor’s specific Standard Operating Procedures (SOPs), contributing intimately to their drug pipeline to become a true “indication and molecule expert.” Because you are allocated to only 1–2 protocols at a time, your workload remains consistent, highly predictable, and stable.
Clinical Research Associate Job – Key Responsibilities
The Clinical Research Associate (CRA) or Senior CRA assumes country-wide responsibility for the operational execution, compliance, and clinical data integrity of allocated investigative sites, acting as the primary hub contact for the single-sponsor study team.
Your core site management, document auditing, and milestone verification duties include:
- Fit-for-Purpose Monitoring Execution: Conducting a blend of remote data checks and targeted on-site monitoring visits, typically spending 6 to 8 days per month on-site depending on sponsor metrics.
- Patient Recruitment Strategy: Working closely with investigative site teams to adapt, drive, track, and optimize localized subject recruitment and retention plans.
- Investigator & Protocol Training: Delivering specialized clinical protocol, compound parameters, and study-specific procedural training to assigned investigators and medical site staff.
- Audit & Report Curation: Generating, maintaining, and finalizing thorough monitoring visit reports and tracking action plans within clinical trial management tools to advance this Clinical Research Associate Job.
- ICH-GCP Quality Assurance: Reviewing source documentation, verifying case report forms (CRFs), and ensuring all site activities are continuously inspection-ready and compliant with international guidelines.
- Peer Mentorship & Onboarding: If appropriate for senior tiers, co-monitoring, training, and mentoring junior members of the regional clinical monitoring team to support a prominent Life Sciences Job.
- Safety & Deviation Triage: Securing the accurate, timely reporting of Serious Adverse Events (SAEs) and protocol deviations in strict alignment with sponsor and regulatory frameworks.
Qualifications & Profile Requirements For Clinical Research Associate Job
IQVIA seeks flexible, highly organized clinical researchers who demonstrate excellent time management habits and an uncompromising approach to Good Clinical Practice (GCP) quality.
- Required Academic & Experience Criteria:
- Educational Foundation: A completed formal University degree in the Life Sciences.
- Industry Track Record: A minimum of 12 months of independent, on-site clinical monitoring experience executed within a CRO or pharmaceutical industry setting to build an IQVIA Career.
- Regulatory Grounding: In-depth, practical working knowledge of international ICH-GCP guidelines and European clinical trial regulations.
- Core Technical & Structural Skills:
- Demonstrated experience handling multiple protocols across a variety of drug indications (with preference given to backgrounds in Oncology, Neurology, Immunology, and/or Diabetes).
- Strong communication, written text composition, and presentation skills with absolute fluency in English.
- Strong digital workspace traits, with comfort navigating remote data check systems, CTMS portals, and electronic Trial Master Files (eTMF).
- Mobility Credentials: Possession of a valid, clean driving license, paired with the complete flexibility to travel nationwide as required by monitoring plans.
- Visa Limitation: Please note – this position is not eligible for visa sponsorship; applicants must hold independent, permanent working rights in Ireland.
In short, the single-sponsor Clinical Research Associate position at IQVIA is a definitive route to transitioning your field monitoring or nursing experience into a highly marketable global asset. Securing an appointment here allows you to move past chaotic multi-protocol environments and take centralized, strategic charge of a focused clinical pipeline, backed by low regional travel thresholds, stable workloads, and structured line management. If you reside in Ireland, meet the 12-month independent monitoring threshold, and possess an uncompromising commitment to data accuracy, apply today to secure this premier Clinical Research Associate Job, launch an exceptional IQVIA Career, and lock in this outstanding Life Sciences Job.
