{"id":4133729,"url":"https://alion.io/job/icon-clinical-pharmacologist","title":"Clinical Pharmacologist","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":86,"open_postings":64,"ghost_share":0,"stale_share":0.75,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-11-12T10:38:37Z"}},"role":"Biotech","role_family":"Biotech","seniority":null,"employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Blue Bell, United States"],"countries":["US"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"experience_years_min":null,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-11-11T00:00:00Z","employer_posted_date":"2026-11-11","last_verified_at":"2026-11-12T10:32:28Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Clinical PharmacologistAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.\nThe CP is aware of and ensures that all activities of the medical team are in compliance with current local and international regulations, laws, guidance (e.g. FDA, ICH, CPMP, etc.), Good Clinical Practices (GCPs), company standards, policies and procedures, and the Principles of Medical Research and are aligned with the medical vision.\nThe CP may be called upon to participate on additional items including but not limited to internal executive and governance presentations, external key opinion leader interactions, medical outreach/advocacy, and industry conferences.\nWhat You Will Do:\nYour role will involve delivering clinical pharmacology and pharmacokinetics work to a high standard, working closely with your team and stakeholders.\nKey responsibilities include:\nContribute to the development of the overall strategy and clinical plan for development of clinical compounds, focusing on studies required for product decision or regulatory submission\nSupport preparation of high-level plan for phase 2 and 3 studies for early phase and/or detailed biopharm plan to support submission• Collaborate with other functional areas (Global Patient Safety, PK/PD, ADME, Statistics, Tailored Therapeutics organization) in the development of methods for assessing special clinical safety pharmacology studies\nCollaborate with other quantitative scientists (e.g., PK/PD, statistics, molecular epidemiology, ADME, modeling and simulations) to integrate study development and conduct with disease-progression and drug disease response models\nContribute, as an integral member of the Clinical Pharmacology team, to global Phase I and II clinical studies as well as submission planning activities\nWork closely with discovery research scientists in the development of basic research strategies, clinical candidate compound selection, and preclinical development\nWork with Brand Team/Business Unit colleagues to provide appropriate market differentiation and regulatory support in the biopharm submission plan\nDesign and oversee implementation of all clinical pharmacology studies. Capabilities include understanding the unique aspects of conducting such studies in healthy volunteers and patient groups/special populations\nApply fundamental concepts of clinical pharmacology and clinical pharmacokinetics to clinical pharmacology research\nDesign and oversee implementation methods for development and biomarker qualification studies\nDesign, create, and provide oversight for protocol development\nSupport development of documents for the conduct of studies in collaboration with functions and operations staff and affiliates in accordance with GCP and local requirements \nCollaborate with local clinical research staff, statisticians, health outcomes research scientists and selected consultants and/or investigators in the development of protocols, and data collection requirements\nParticipate in investigator identification and selection, in conjunction with the clinical pharmacology sourcing group\nYour Profile:\nRequired qualifications and experience:\nLife science degree (MD, PhD, PharmD) with requisite experience in Clinical Pharmacology \nPhD preferrable but not required\nExperience in Pharmaceutics and Product Design preferrable\nKnowledge of and experience in Clinical Pharmacology and drug development process preferred\nFluent in English; both written and verbal communications\nInterpersonal, organizational and negotiation skills\nAbility to influence others (both cross-functionally and within the function) in order to create a positive working environment\nExcellent teamwork skills\nWilling to engage in domestic and international travel to the degree appropriate to support the business of the team\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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