Clinical Scientist

Worldwide Clinical Trials

. Develop oncology clinical data review plans for assigned studies .

Posted 9/18/2026full-timeRemote • Illinois • United StatesSeniorLead💰 $79,000 - $157,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in oncology clinical data review and analysis, with a strong understanding of oncology clinical development processes, regulatory requirements, and data visualization tools. Capable of effectively communicating data insights and collaborating with cross-functional teams to ensure accurate reporting and protocol adherence.

Highest-signal resume keywords

Oncology Clinical Data AnalysisElectronic Data Capture (EDC) SystemsData Visualization ToolsRegulatory Requirements (GCP, ICH)Advanced Clinical or Scientific Degree

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Oncology Clinical Development ProcessesClinical Data ReviewData InterpretationSafety Event TrackingStudy Design PrinciplesClinical Reporting Documents ReviewData Quality PlansScientific WritingClinical Understanding of Oncology Disease StatesData Summary Creation

Soft Skills

Excellent Communication SkillsOrganizational AbilitiesAnalytical SkillsProblem-Solving AbilitiesInterpersonal Skills

Tools & Technologies

Microsoft Office SuiteVisual Analytics ToolsData Management SystemsClinical Review ToolsData Review Platforms

Certifications & Qualifications

Advanced Clinical or Scientific Degree (PharmD, PhD, MSN, ARNP)

Industry Keywords

OncologyClinical TrialsPharmacovigilanceSolid TumorsLiquid TumorsBi-Specific AntibodiesCAR-TClinical Study Reports (CSRs)Investigational New Drug Applications (INDs)New Drug Applications (NDAs)

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Develop oncology clinical data review plans for assigned studies
Conduct ongoing oncology clinical data review and analysis, including efficacy and safety-related data, using listings, visual analytics, tables, figures, graphs, and EDC
Present key oncology data trends and findings to the Medical Monitor, Study Team, and Client
Collaborate with cross-functional study team members to ensure protocol-defined variables are collected and reported accurately
Track and analyze potential safety events with Pharmacovigilance and Medical Monitoring
Contribute to discussions on potential study or strategy modifications based on clinical data review
Create data summary slides for Safety Review Committee Meetings and Data Review Meetings
Query EDC data during clinical review, follow up promptly, and identify potential protocol deviations
Partner with vendors and study team members to ensure accurate endpoint reporting
Serve as a point of contact for site staff and monitors for protocol and clinical inquiries
Collaborate with Data Management on CRF design, CRF instructions, and data quality plans
Review data-driven sections of regulatory and clinical reporting documents, including CSRs, INDs, NDAs/BLAs, annual reports, and IBs
Provide scientific writing support for patient narratives, abstracts, posters, and presentations
Mentor and train junior staff
Utilize visual analytics tools to interpret and communicate data insights

Requirements

What you’ll need

Strong knowledge of oncology clinical development processes and study design principles
Deep understanding of oncology product profiles and safety concepts, including DCs, bi-specific antibodies, and CAR-T
Experience with solid tumors, liquid tumors, and imaging clinical data review
Clinical understanding of physiological and pathological effects of oncology disease states and anticancer therapies on human organ systems
Skilled in oncology clinical data analysis, interpretation, and assessing clinical relevance in human clinical trials
Proficiency with electronic data capture systems and data visualization tools
Solid understanding of GCP, ICH guidelines, and regulatory requirements
Excellent written, oral communication, and presentation skills
Strong organizational, analytical, and problem-solving abilities
Ability to manage multiple priorities and adapt to changing demands
Strong interpersonal skills and ability to collaborate across teams and levels
Demonstrated ability to work independently and within teams
Good judgment and decision-making skills
Willingness to travel as needed
Advanced clinical or scientific degree preferred, such as PharmD, PhD, MSN, or ARNP
8+ years of industry-related experience in Oncology
Proficiency in Microsoft Office Suite
Experience with EDC systems and data visualization platforms

Benefits

Comp & perks

Competitive benefits package depending on location
Transparent compensation and pay equity
Inclusive and equitable workplace