Clinical Research Associate Jobs in Ireland

Clinical Research Associate at Merck in Dublin. Responsible for site management, monitoring, compliance with ICH-GCP, SOPs, local regulations.

IQVIA's Site Management team seeks a Clinical Research Associate in Ireland to support Oncology studies across Ireland and Northern Ireland, performing site monitoring visits, managing study progress, ensuring GCP compliance, and collaborating with study teams.

ProPharma seeks a Serbian-speaking Clinical Research Associate for an 18‑month fixed‑term contract. Responsible for monitoring clinical sites in person and remotely, conducting study start‑ups, developing monitoring documentation, reviewing source documents and case reports, managing investigational supplies, monitoring enrollment and adverse events, reviewing regulatory documents, communicating with site personnel and cross‑functional teams, and participating in project meetings.

IQVIA Site Management team accelerates innovation for a healthier world by providing full‑service, multi‑sponsor clinical research support. The Clinical Research Associate II conducts site monitoring visits, drives subject recruitment, ensures regulatory compliance, and manages study documentation across assigned sites.

Clinical FSP Business at IQVIA focuses on delivering high‑quality clinical research services for single sponsor partners. The Clinical Research Associate manages site monitoring, recruitment plans, and protocol training across Ireland, working 6‑8 onsite days per month with remote monitoring support.

Clinical Research Associate II – Ireland: IQVIA’s Site Management team seeks an experienced associate to support oncology studies across Ireland and Northern Ireland. The role involves performing site monitoring visits, ensuring compliance with Good Clinical Practice and ICH guidelines, and driving subject recruitment.

IQVIA Site Management team drives clinical research forward by monitoring trial sites to ensure compliance with GCP and ICH. The Experienced Clinical Research Associate conducts site visits, manages recruitment plans, and maintains trial master files, ensuring data integrity and regulatory adherence. Based in Dublin, Ireland, the role requires on‑site presence with flexible travel to sites.

Kickstart your career in clinical research with IQVIA. As a Clinical Research Intern on the Site Management team, you will assist clinical trials, receive CRA training, and work toward becoming a Clinical Research Associate.

Eli Lilly Cork’s Global Statistical Sciences department seeks a PhD Statistician intern to support the Clinical Statistics team on innovative clinical trial design projects. The role offers a 12‑week hybrid internship based in Little Island, Cork, with a start in May or June 2026.

A seasoned Associate Research Scientist with over five years of experience in analytical testing laboratories and GMP environments. Skilled in HPLC/Chromatography, GC, LC/MS, and oligonucleotide analysis, this professional excels in method development, validation, and troubleshooting.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Technical Project Manager - ARS At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer.

Associate Clinical Development Director (Neurosciences) at Novartis leads scientific and clinical strategy for assigned trials, overseeing trial documents, regulatory submissions, and safety reporting. The role requires advanced life sciences degree and 5+ years in clinical research across Phases I-IV, with at least 2 years of end-to-end trial execution in a global pharmaceutical setting.

Associate Clinical Development Director (VHB) at Novartis leads clinical strategy and scientific oversight for global neuroscience trials. The role drives protocol development, trial documentation, and regulatory submissions, collaborating with Clinical Trial Team and Medical Lead.

TMF Operations team ensures trial documentation accuracy, compliance, and quality in a global clinical research environment. The Senior Associate II manages TMF operations, oversees quality control processes, prepares KPIs, supports audits, and collaborates with project teams and sponsors.

Senior Clinical Development Medical Director leads scientific and clinical strategy for assigned trials, oversees data review, and drives program execution. Works in hybrid model across London and Dublin, collaborating with global line functions, trial directors, and medical associates.

Senior Clinical Development Director leading strategic planning and execution of cardiovascular/metabolic clinical programs. Oversees clinical deliverables, regulatory documents, safety reporting, and cross‑functional collaboration with Global Trial Directors, medical associates, and scientific experts.

Clinical Development Medical Director – CRM leads a clinical program section or large trial, providing strategic medical input and overseeing deliverables such as protocols, data reviews, regulatory dossiers, and publications. The role partners with global line functions, Global Trial Directors, and regional medical associates to execute program sections, conduct medical and scientific reviews with Clinical Scientific Experts, and monitor safety through the Safety Management Team.

Clinical Development Medical Director - Cardiovascular at Novartis leads clinical programs in cardiovascular therapeutics, overseeing protocol development, data review, regulatory documentation, and publications. The role drives execution with global line functions, trial directors, and regional associates, and conducts medical and scientific reviews of trial data.

Clinical Development Medical Director at Novartis leads end‑to‑end clinical development for cardiovascular programs. The role oversees clinical leadership, strategic medical input, and regulatory documentation across global teams.

Senior Clinical Development Medical Director (CDMD) leads strategic planning and management of renal clinical programs, overseeing end-to-end development, regulatory documentation, and safety reporting. Works with global line functions, GTDs, and regional medical associates to execute trials, provide medical input into plans and protocols, and support clinical development leadership.