What the Clinical Scientist does at Worldwide As a member of the Clinical Oncology Operations team, the Clinical Scientist leads the review and assessment of clinical data, ensuring it meets the highest standards of quality and integrity. This role translates complex data into clear insights, communicates trends to internal teams and clients, and supports the development of key regulatory deliverables such as clinical study reports. Working closely with cross-functional stakeholders, the Clinical Scientist helps drive timely project delivery, contributes to data review strategies, and identifies opportunities to improve processes and elevate overall study execution.
What you will do - Partner with cross-functional Study Teams (Medical, Biostatistics, Data Management) to develop and execute data review plans, ensuring accurate collection and reporting of protocol-defined endpoints.
- Perform ongoing review and interpretation of clinical data (efficacy and safety) across listings and visual analytics, identifying trends and generating actionable insights.
- Monitor and analyze safety events across studies and programs, supporting risk identification, escalation, and informed decision-making.
- Communicate and present clinical findings, trends, and recommendations to Study Teams, Medical leadership, and clients; contribute to strategic discussions and study modifications.
- Support 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 meetings.
- Collaborate on CRF design, data quality processes, and EDC query management; identify protocol deviations and ensure data integrity in partnership with internal teams and vendors.
- Contribute to study execution and continuous improvement efforts, including dashboard/UAT support, study documentation, scientific writing (e.g., narratives, abstracts), and mentoring of junior staff.
What you will bring to the role - Strong knowledge of the clinical development process, study design principles, and product safety profiles.
- Experience in clinical data analysis, interpretation, and translating insights into clinical relevance.
- Proficiency with electronic data capture (EDC) systems, data visualization tools, and Microsoft Office (Excel, PowerPoint, Word).
- Solid understanding of GCP, ICH, and applicable regulatory requirements.
- Excellent communication and presentation skills, with the ability to convey complex data clearly to diverse stakeholders.
- Strong organizational, analytical, and problem-solving skills, with the ability to manage multiple priorities and meet deadlines.
- Collaborative, adaptable team player with strong interpersonal skills and the ability to work effectively across all levels of an organization.
- Sound judgment, high attention to detail, and the ability to work both independently and in fast-paced, evolving environments.
Your experience - Advanced clinical/science degree (e.g., PharmD, PhD, MSN, MPH, etc.) preferred.
- 8+ of industry/related experience in Oncology human clinical trial research including review and interpretation of clinical data.
