Clinical Investigator Management 

• Accountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout 

• Serve as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements 

• Develop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas 

• Influence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives 

• Proactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc 

• Capture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct 

Clinical Trial Management 

• Lead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery 

• Leverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones 

• Drive inspection readiness as a continuous discipline across sites 

• Collaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality 

• Maintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization 

• Provide oversight and quality assurance for vendor monitoring, escalating risks proactively 

• Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations 

• Business Management and Engagement 

• Cultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials 

• Enable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner 

• Collaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity 

• Conduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution 

• Maintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel 

• Act as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer 

• Partner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships 

You are:

• Bachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields 

• Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites  

• Open to up to 60-80% travel during peak times (travel will vary)

• Oncology experience required (Breast/Gyn experience preferred)

• Location: Mid-Atlantic, Southeast Region