Business Development Associate (Clinical Research – Pipeline & Opportunity Development).

Angel City VA; United States; Remote; USD 70.000 - 90.000; Vollzeit

Zusammenfassung

Angel City VA is looking for a Business Development Associate to lead the identification and management of clinical trial opportunities. This role is crucial for advancing studies aligned with the organization's capabilities. Responsibilities include conducting due diligence on sponsors, developing outreach strategies, and ensuring operational compliance, all while maintaining quality pipeline tracking. The ideal candidate should possess strong analytical and communication skills, alongside proficiency in tools such as Microsoft Excel and SharePoint.

Qualifikationen

• Strong analytical capability for data interpretation and trend analysis.
• High attention to detail and organizational discipline.
• Ability to synthesize complex clinical and market data.

Aufgaben

• Identify and qualify clinical trial opportunities.
• Conduct due diligence on sponsors and CROs.
• Perform early-stage study evaluations.

Kenntnisse

Analytical capability

Attention to detail

Communication skills

Research-driven mindset

Tools

Microsoft Excel

Microsoft Word

G Suite

SharePoint

Microsoft Teams

Jobbeschreibung

Business Development Associate (Clinical Research – Pipeline & Opportunity Development)

The Business Development Associate is responsible for end-to-end pipeline development and opportunity intelligence within the clinical research lifecycle. This role focuses exclusively on identifying, evaluating, qualifying, and advancing clinical trial opportunities aligned with organizational capabilities and therapeutic priorities.

This position does not include responsibilities related to budget development, contract negotiation, or financial structuring. Instead, it serves as a front-end engine for study acquisition, ensuring a high-quality, strategically aligned pipeline for downstream feasibility and contracting team members.

Core Responsibilities

1. Clinical Trial Opportunity Identification & Pipeline Development.
   • Systematically identify new clinical trial opportunities through: ClinicalTrials.gov, GlobalData, sponsor and CRO websites, industry portals, and targeted search strategies.
   • Maintain a centralized opportunity tracker (Excel/SharePoint-based) with real-time updates on: study status, sponsor/CRO, therapeutic area, phase, and timelines.
   • Build and manage a qualified pipeline aligned with organizational enrollment capabilities and therapeutic focus areas.
2. Sponsor & CRO Intelligence and Evaluation.
   • Conduct structured due diligence on sponsors and CROs, including financial stability, therapeutic area strategy, pipeline depth, and historical trial execution patterns.
   • Generate sponsor profiles to guide prioritization and outreach strategy.
3. Study Feasibility Pre-Assessment (Non-Financial).
   • Perform early-stage study evaluation to determine organizational fit in terms of therapeutic area alignment, investigational product type (drug, device, biologic), and study phase (priority on Phase II-IV).
   • Analyze protocol-level elements: inclusion/exclusion criteria, visit schedules, procedural burden, and study design complexity.
   • Translate findings into actionable go/no-go recommendations for internal stakeholders.
4. Investigator & Patient Population Matching.
   • Conduct targeted research to align studies with investigator expertise, existing and potential patient populations, and diagnosis mapping using ICD frameworks.
   • Support high-probability enrollment scenarios based on disease prevalence, site capabilities, and historical performance indicators.
5. Strategic Intelligence & Market Analysis.
   • Monitor and interpret trends across therapeutic areas, emerging indications, sponsor investment patterns, and competitive site activity.
   • Identify high-value therapeutic opportunities and provide strategic recommendations to leadership.
   • Produce insight summaries and pipeline reports for executive review.
6. Targeted Outreach Strategy Development.
   • Develop highly tailored outreach approaches for sponsors and CROs, aligning messaging with study protocol specifics, investigational product characteristics, and target patient populations.
   • Customize communication based on stakeholder type: sponsor executives, clinical operations teams, CRO representatives.
   • Ensure all outreach reflects clinical relevance, operational readiness, and strategic fit.
7. Contact Identification & Relationship Mapping.
   • Identify and validate key decision-makers using LinkedIn, GlobalData, sponsor/CRO websites, RocketReach, and advanced search methodologies.
   • Build and maintain a clean, structured contact database for outreach execution.
8. SOP Adherence & Operational Compliance.
   • Execute all responsibilities in strict accordance with organizational SOPs: naming conventions, documentation standards, and workflow processes.
   • Ensure audit-ready documentation of all pipeline activities and evaluations.

Required Skills & Technical Proficiency

Systems & Tools

• Microsoft Excel
• Microsoft Word
• G Suite (Docs, Sheets, Drive)
• SharePoint & OneDrive
• Microsoft Outlook
• Dropbox
• Microsoft Teams / Zoom

Core Competencies

• Strong analytical capability (data interpretation, pattern recognition, trend analysis)
• High attention to detail and organizational discipline
• Ability to synthesize complex clinical and market data into clear recommendations
• Strong written and verbal communication skills
• Research-driven mindset with structured, repeatable workflows
• Ability to rapidly learn clinical terminology, therapeutic areas, and protocol structures

Preferred Qualifications

• Experience in clinical research, CROs, or healthcare business development
• Familiarity with clinical trial design and phases, ICD coding systems, and therapeutic areas such as metabolic disease, GI, wound care, or cardiovascular conditions
• Experience using clinical intelligence platforms and pipeline tools

Key Performance Indicators (KPIs)

• Volume and quality of identified trial opportunities
• Pipeline growth rate and alignment with organizational priorities
• Accuracy and depth of sponsor and study evaluations
• Conversion of identified opportunities to feasibility engagement
• Quality and effectiveness of targeted outreach strategies
• Timeliness and completeness of pipeline tracking and reporting

Role Boundaries (Explicit Exclusions)

• Budget development
• Contract negotiation
• Financial feasibility analysis

Position Impact

This role functions as a strategic intake and qualification layer within the clinical trial acquisition funnel—directly influencing the organization’s ability to secure high-quality studies, optimize enrollment potential, and align with sponsors that match long-term growth strategy.