Life Sciences Project Lead

Target RWE•Research Triangle Park, NC

7d•Hybrid

About The Position

At Target RWE, our mission is driven by a deep commitment to people, whether it’s the patients we serve, the partners we collaborate with, or the dedicated team members who power our work. As a purpose-driven organization, we leverage real-world data to advance clinical research and inform better healthcare decisions. We foster a collaborative environment where every voice is heard, every idea has impact, and every contribution helps improve lives. If you are seeking a place where your work truly matters, join us to advance science. Overview The Life Sciences Project Lead bridges ambitious strategy and flawless execution. In this role, you will own the end-to-end delivery of complex Real-World Evidence (RWE) initiatives, transforming scoped contracts into high-impact clinical insights. You will be responsible for navigating study design, clinical analytics, and stakeholder management to ensure every deliverable meets the highest standards of quality and scientific rigor. This is a high-velocity role for a leader who thrives in dynamic environments, takes full ownership of outcomes, and drives projects forward with precision and accountability.

Requirements

5+ years of experience in life sciences services, health tech, or healthcare consulting, with a track record of managing multi-stakeholder engagements
Deep knowledge of the life sciences ecosystem, including RWE, clinical operations, and analytics
Demonstrated ability to lead complex, data-intensive projects under tight timelines without compromising quality
Strong executive presence and the ability to translate technical and clinical complexity for diverse audiences

Nice To Haves

Exposure to data-intensive platforms or AI/ML-driven healthcare products
Familiarity with Agile, hybrid, or scaled project delivery methodologies

Responsibilities

Lead the full lifecycle of RWE projects from post-sale handoff through final delivery, ensuring milestones are met on time and within budget
Optimize speed, cost, and quality through standardized processes, system updates, and rigorous compliance protocols
Identify opportunities to accelerate timelines while maintaining scientific and operational excellence
Serve as the internal voice of the client, translating sponsor requirements into actionable plans for Product, Engineering, Quantitative Sciences, and Clinical teams
Set clear objectives for project teams, providing leadership and feedback to maintain high performance
Ensure all initiatives adhere to data governance, privacy standards, and regulatory requirements
Act as the primary client contact for biopharma sponsors, managing relationships across clinical, data science, and executive stakeholders
Proactively identify quality or delivery risks and develop contingency plans
Serve as the senior escalation point for project-critical issues
Maintain transparent success metrics and governance structures to provide real-time project health visibility