Remote Clinical Scientist Oncology US Remote

Note: The job is a remote job and is open to candidates in USA. Worldwide Clinical Trials is a global, midsize CRO focused on innovative approaches to improve lives. The Clinical Scientist leads the review and assessment of clinical data in oncology, ensuring quality and integrity while supporting regulatory deliverables and project delivery through collaboration with cross-functional teams.ResponsibilitiesPartner with cross-functional Study Teams (Medical, Biostatistics, Data Management) to develop and execute data review plans, ensuring accurate collection and reporting of protocol-defined endpointsPerform ongoing review and interpretation of clinical data (efficacy and safety) across listings and visual analytics, identifying trends and generating actionable insightsMonitor and analyze safety events across studies and programs, supporting risk identification, escalation, and informed decision-makingCommunicate and present clinical findings, trends, and recommendations to Study Teams, Medical leadership, and clients; contribute to strategic discussions and study modificationsSupport development of key deliverables, including clinical study reports (CSRs), regulatory documents (e.g., INDs, NDAs/BLAs, IBs), and data summaries for SRCs, DSMBs, and internal review meetingsCollaborate on CRF design, data quality processes, and EDC query management; identify protocol deviations and ensure data integrity in partnership with internal teams and vendorsContribute to study execution and continuous improvement efforts, including dashboard/UAT support, study documentation, scientific writing (e.g., narratives, abstracts), and mentoring of junior staffSkillsStrong knowledge of the clinical development process, study design principles, and product safety profilesExperience in clinical data analysis, interpretation, and translating insights into clinical relevanceProficiency with electronic data capture (EDC) systems, data visualization tools, and Microsoft Office (Excel, PowerPoint, Word)Solid understanding of GCP, ICH, and applicable regulatory requirementsExcellent communication and presentation skills, with the ability to convey complex data clearly to diverse stakeholdersStrong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities and meet deadlinesCollaborative, adaptable team player with strong interpersonal skills and the ability to work effectively across all levels of an organizationSound judgment, high attention to detail, and the ability to work both independently and in fast-paced, evolving environmentsAdvanced clinical/science degree (e.g., PharmD, PhD, MSN, MPH, etc.) preferred8+ of industry/related experience in Oncology human clinical trial research including review and interpretation of clinical dataCompany OverviewWorldwide Clinical Trials is a global CRO that provides preclinical and Phase I-IV clinical development services to pharmaceutical industry. It was founded in 1986, and is headquartered in Morrisville, North Carolina, USA, with a workforce of 1001-5000 employees. Its website is https://www.worldwide.com.Company H1B SponsorshipWorldwide Clinical Trials has a track record of offering H1B sponsorships, with 1 in 2024, 5 in 2023, 3 in 2022, 2 in 2021, 2 in 2020. Please note that this does not guarantee sponsorship for this specific role. Apply To this Job .