Clinical Insights Solutions Lead, Data & Insights

🔥 1 minute ago

🇺🇸 United States – Remote

💵 $92k - $143k / year

⏰ Full Time

🟠 Senior

📊 Data Scientist

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WCG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💊 Pharmaceuticals

☁️ SaaS

💰 Private Equity Round - WCG on 2019-11

Healthcare • Pharmaceuticals • SaaS

WCG is a global clinical research services and technology company that supports sponsors, CROs, research sites, and institutions across the lifecycle of clinical trials. Founded as a leader in independent ethical review, WCG provides IRB and IBC review, data monitoring committees, site enablement and study start-up services, participant recruitment and retention, and data & insights (including benchmarking, statistical consulting, and AI-powered trial foresight). The company also offers a suite of technology platforms (e. g. , ClinSphere®, eReview Manager, Total Enrollment, Total Feasibility) and large protocol and performance datasets to help design, plan, and run trials more efficiently and compliantly. WCG positions itself as a partner to biopharma and medical research organizations to accelerate trial activation, improve enrollment, and ensure regulatory and ethical compliance.

📋 Description

• 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

• 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

• 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

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