{"id":3725120,"url":"https://alion.io/job/icon-clinical-scientist","title":"clinical scientist","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":85,"open_postings":58,"ghost_share":0,"stale_share":0.81,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-11-06T05:58:05Z"}},"role":"Science & Research","role_family":"Science & Research","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","Burlington, Canada"],"countries":["US","CA"],"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":[],"status":"live","first_seen_at":"2026-11-02T00:00:00Z","employer_posted_date":"2026-11-02","last_verified_at":"2026-11-06T06:27:57Z","board_verified":true,"closed_at":null,"days_open":4,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":4},"description":"Clinical ScientistAt 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.\nAs a Clinical Scientist at ICON, you will design and conduct clinical studies that advance our understanding of new therapies.\nWhat You Will Do:\nYou will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.\nKey responsibilities include:\nDesigning and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards.\nConducting data analysis and interpretation to derive insights that support study objectives.\nCollaborating with cross-functional teams to ensure effective study execution and data quality.\nEngaging with stakeholders to communicate findings and contribute to scientific discussions.\nAssisting in the preparation of regulatory submissions, study reports, and scientific publications.\nYour Profile:\nYou will bring relevant clinical research experience, along with the following qualifications and skills.\nRequired qualifications and experience:\nBachelor's degree in a relevant scientific discipline or healthcare-related field\nExperience in clinical research or a related scientific role, with a strong understanding of clinical trial processes.\nExcellent analytical skills and proficiency in data interpretation and statistical analysis.\nStrong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams.\nDetail-oriented and committed to maintaining high standards of data integrity and quality.\nWillingness to travel as required (approximately 20%)\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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