10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
đ„ 14 hours ago
Where this job comes from
Posted on ICON plc's careers page, not through a job board
First seen by Remote Rocketship 14 hours ago
Still open on ICON plc's site. Checked 37 minutes ago.
10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą Logistics
ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.
âą Ensure all medical team activities comply with current local and international regulations, laws, guidance, Good Clinical Practices, company standards, policies and procedures, and the Principles of Medical Research âą Participate in internal executive and governance presentations, external key opinion leader interactions, medical outreach/advocacy, and industry conferences âą Deliver clinical pharmacology and pharmacokinetics work to a high standard âą Contribute to overall strategy and clinical plans for development of clinical compounds, focusing on studies required for product decisions or regulatory submissions âą Support high-level plans for Phase 2 and 3 studies and detailed biopharm plans for submissions âą Collaborate with Global Patient Safety, PK/PD, ADME, Statistics, Tailored Therapeutics and other quantitative science functions âą Integrate study development and conduct with disease-progression and drug-disease response models âą Contribute to global Phase I and II clinical studies and submission planning âą Work with discovery research scientists on basic research strategies, clinical candidate selection and preclinical development âą Provide market differentiation and regulatory support in biopharm submission plans âą Design and oversee clinical pharmacology, biomarker qualification and development studies âą Develop, create and oversee study protocols and supporting documents in accordance with GCP and local requirements âą Collaborate with clinical research staff, statisticians, health outcomes research scientists, consultants and investigators on protocols and data collection requirements âą Participate in investigator identification and selection
âą Life science degree (MD, PhD, PharmD) with requisite experience in Clinical Pharmacology âą Experience in Clinical Pharmacology âą Fluent in English; both written and verbal communications âą Interpersonal, organizational and negotiation skills âą Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment âą Excellent teamwork skills âą Willing to engage in domestic and international travel to the degree appropriate to support the business of the team âą Employment with ICON is contingent upon having the legal right to work in the country where the role is based
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
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