Sr. Clinical Scientist (Hybrid-NYC)

*Must work onsite in New York, NY 10016, 3x per week*As a Senior Clinical Scientist you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.What you will be doing:Responsible for leading specific aspects of clinicalscientific execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial teamLeading medical monitoring team in review and interpretation of clinical datamedical protocol deviations in collaboration with Clinical Research and PharmacovigilanceCollaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents amendments); partnering with Clinical Operations on study deliverablesEnsure CRF design supports data collection in alignment with the Protocol in collaboration with Clinical Data ManagementProgrammingCollaborating cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conductProviding tacticalscientific mentorship to other clinical scientistsResponsible for assisting with the generation, analysis, and presentation of clinical data, including manuscripts, abstracts, and oral presentations (including authoring documents and slide preparation as appropriate)Apply proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; identifies risks and designs mitigation strategiesPromotes consistent first line medicalclinical data review techniques and conventions across studiesprograms.You are:At least 5 years of relevant experienceMaster's degree in life sciences + 3 years clinical drug development experience, or PhD, Pharm D, RN degreeOncology experience requiredExperience leading a medical monitoring team requiredSolid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)Ability to manage multiple competing priorities with good planning, time management and prioritization skillsStrong analytical skills with the ability to interpret clinical trial data and synthesize conclusionsProficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents related to clinical trials, such as medical monitoring plan, SAPs, informed consent and clinical components of the Clinical Study ReportsInteract with key stakeholders across Clinical Development functional areasRole requires proactive approach, strategic thinking and leadership in driving toward clinical study goalsInfluence opinions and decisions of internal and external customers vendors, across functional areasProblem solving, prioritization, conflict resolution and critical thinking skillsStrong communication, technical writing, and presentation skills experienceWhat ICON can offer you:Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:Various annual leave entitlementsA range of health insurance offerings to suit you and your family's needsCompetitive retirement planning offerings to maximize savings and plan with confidence for the years aheadGlobal Employee Assistance Program, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Created: 2024-11-01