Clinical Research Scientist - Cardio Metabolic Health Development
Eli Lilly and Company is seeking a Clinical Research Scientist for Cardio Metabolic Health Development. Join a global healthcare leader focused on discovery and life-changing medicines. Lilly Cork employs a diverse team across multiple functions and offers flexible hybrid working options and comprehensive benefits.
Overview
Location: Little Island, Cork, Ireland. This role supports late-phase and marketed compounds, focusing on clinical planning, execution, data dissemination, regulatory support, and strategic medical activities to enable product value and access.
Primary Responsibilities
* Apply scientific and clinical training to develop, conduct, and report global clinical trials in support of product registration and commercialization.
* Implement global clinical trials and report adverse events per corporate patient safety policies.
* Review protocols, study reports, publications, and data for products, pricing, reimbursement, and access documentation; liaise with regulatory and governmental agencies.
* Engage in outreach to external clinical customers, thought leaders, and colleagues; help shape business unit and global product strategy.
* Ensure compliance with regulations, GCPs, Lilly policies, and the medical vision.
Clinical Planning
* Collaborate across regions and teams to develop Launch Label and Value Proposition; align clinical strategy with lifecycle plans and study design.
* Update and maintain clinical plans and data relevant to the molecule.
Clinical Research/Trial Execution and Support
* Plan and review scientific content of clinical documents (protocols, informed consent, final study reports, submissions) per timelines.
* Provide protocol oversight and input on informed consent documents.
* Monitor patient safety and participate in global product safety reviews; track and follow up on adverse events.
* Collaborate on local clinical trial design, conduct, and reporting; manage risk communication to subjects.
* Support investigator identification, site initiation, and regulatory/compliance processes (GCPs, local laws).
* Train investigators and site personnel; serve as resource to clinical operations and monitors.
Scientific Data Dissemination / Exchange
* Ensure compliance with laws, global policies, and data dissemination guidelines for external interactions.
* Manage unsolicited scientific information requests and support data dissemination planning, symposia, and publications.
* Build collaborations with external experts and professional societies; support medical information and congress activities.
Regulatory Support
* Develop and review label changes with affiliates and regulatory teams; provide medical expertise to regulatory scientists.
* Assist in regulatory submissions and regulatory issue resolutions from a global perspective; participate in advisory committees.
Business / Customer Support (Pre- and Post-Launch)
* Contribute to medical strategies to support brand commercialization; collaborate with cross-functional teams on local business plans.
* Anticipate scientific information needs of customers (payers, patients, providers); address questions with data analyses and outcomes research.
* Develop payer partnerships and support B2B/B2G activities as a medical expert; contribute to brand strategy and promotional materials as needed.
* Lead in defining the Patient Journey and Moments of Truth; engage as a patient advocate and medical expert.
Technical Expertise & Development
* Critically read and evaluate medical literature; stay updated on product-relevant science and market developments.
* Provide scientific training to the clinical study team and act as protocol expert.
* Monitor trends in clinical practice and explore extramural scientific opportunities; participate in scientific symposia and training.
General Responsibilities
* Set and pursue professional development goals; contribute to others’ development.
* Support budget preparation and administration for the business unit.
* Participate in recruitment, diversity, retention efforts, and cross-functional partnerships.
* Provide constructive feedback, participate in committees and improvement initiatives.
* Maintain up-to-date training and act as an ambassador for patients and Lilly.
Minimum Qualification Requirements
* Advanced health/medical/scientific degree (e.g., Pharmacology, Physiology, Microbiology) or related graduate degree such as DVM, PharmD, PhD, MSN with clinical specialty; 3–5 years of clinical or pharmaceutical experience (2 years in clinical development).
* Or a BS/MS with 7–10 years of pharmaceutical experience related to clinical trials, drug discovery, or development; demonstrated medical content ownership and endorsement by senior leadership; strong communication and leadership skills; travel ability; English fluency.
Lilly is dedicated to equal opportunity and will provide accommodations in the application process upon request.
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Location: Little Island, Cork, Ireland. 19 hours ago
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