Clinical Insights Solutions Lead, Data & Insights

WCG

. Serve as a strategic analytics partner throughout the commercial process .

Posted 11/3/2026full-timeRemote • United StatesSenior💰 $91,980 - $143,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research analytics, including feasibility assessments, site selection, and operational benchmarking. Proficient in translating complex data insights into actionable strategies while effectively communicating with stakeholders across various therapeutic areas.

Highest-signal resume keywords

Clinical Research AnalyticsFeasibility AssessmentsSite SelectionSQL AnalysisData Visualization

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial IntelligenceOperational AnalyticsData AnalysisBenchmarking MethodologyEnrollment ModelingProtocol Deep-DivesStatistical AnalysisEpidemiologyOperational Performance AnalysisCompetitive Trial Landscape Assessments

Soft Skills

Communication SkillsStorytelling SkillsConsultative SkillsCoaching SkillsPresentation Skills

Tools & Technologies

SQLPythonRCTMSEDCMicrosoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft OutlookCRM Platforms

Certifications & Qualifications

ACRPSOCRAPMPData Science CertificationAnalytics Certification

Industry Keywords

Life SciencesEpidemiologyBiostatisticsHealth EconomicsClinical Trial Data SourcesICH-GCPFDA RegulationsOncologyRare DiseaseCell and Gene Therapy

Tech Stack

Tools & technologies

PMPPythonSQL

About the role

Key responsibilities & impact

Serve as a strategic analytics partner throughout the commercial process
Collaborate with Business Development to translate sponsor and CRO questions into data-driven insights
Evaluate study placement, site enrollment potential, and historical operational performance
Scope and execute site targeting, site identification, operational benchmarking, protocol deep-dives, competitive trial landscape assessments, and enrollment feasibility modeling
Present findings directly to clients and explain methodology and limitations
Qualify client needs and scope data, analytics, and advisory solutions
Participate in client meetings, capability presentations, product demonstrations, bid defenses, and strategic workshops
Author data and insights content for proposals, RFI and RFP responses, and follow-up materials
Design and execute site identification analyses using trial landscape data, investigator performance history, epidemiology, referral patterns, and site-level operational metrics
Build ranked site and country lists with explicit selection logic
Assess site capability against protocol-specific requirements
Identify concentration risk, competing-trial overlap, and over-solicited sites
Produce operational performance analyses and benchmark comparable studies
Apply and document benchmarking methodology
Diagnose historical underperformance and develop actionable mitigations
Maintain reusable libraries of benchmarks, assumptions, and analytical templates
Conduct protocol deep-dives and quantify impacts on screen failures, site burden, patient dropout, and start-up delay
Model operational trade-offs of protocol alternatives
Translate protocol requirements into enrollment models and timeline scenarios
Pressure-test conclusions with therapeutic, regulatory, and ethical subject matter experts
Feed engagement-related data and tooling gaps back to Data Engineering and Product
Document methodology and maintain version control for reproducible, auditable results
Conduct post-award and post-loss reviews of analytical assumptions
Coach Business Development colleagues and junior analysts
Participate in webinars, podcasts, conference sessions, and thought leadership activities
Perform other duties as assigned

Requirements

What you’ll need

Bachelor’s degree in life sciences, epidemiology, biostatistics, health economics, data science, or a related quantitative field is required
5+ years of experience in clinical research, clinical trial intelligence, or healthcare data and analytics
At least 3 years in a role centered on feasibility, site selection, operational analytics, or clinical data analysis
Demonstrated experience working directly with sponsor- or CRO-side stakeholders in a pre-sale, consultative, or advisory capacity
Practical familiarity with clinical trial data sources, including trial registries, investigator and site databases, CTMS and EDC outputs, claims and EHR-derived real-world data, and published literature
Experience across multiple therapeutic areas and study phases
Hands-on analysis using SQL and at least one analytical environment, such as Python or R, or equivalent advanced business intelligence, visualization, and modeling tools
Ability to explain methodology and uncertainty to a non-technical audience
Strong data visualization and storytelling skills
Ability to communicate data limitations objectively and distinguish evidence-supported conclusions from assumptions
Ability to work to compressed proposal deadlines across several concurrent opportunities
Ability to present complex analyses credibly and effectively to senior internal and external stakeholders
Working knowledge of ICH-GCP and FDA regulations as they relate to research
Must be able to maintain confidentiality of client, sponsor, and site-level data
Advanced knowledge of Microsoft Word, Excel, PowerPoint, Outlook, and CRM platforms
Advanced degree (MSc, MPH, MBA, PhD, PharmD) preferred
ACRP/SOCRA, PMP, or a recognized data science or analytics certification preferred
Exposure to oncology, rare disease, or cell and gene therapy is an advantage

Benefits

Comp & perks

Medical, dental, vision, life and disability insurance
401(k) with company match
Flexible spending accounts
Employee assistance programs
Work/life balance tools
Referral bonuses
Tuition reimbursement
On-the-job training
Certification assistance
Continuing education support
Paid holidays
Vacation
Sick time
Career development opportunities across One WCG