Associate Site & Patient Access Strategist

Overview

Associate Site & Patient Access StrategistBe Part of One Team, One Purpose.At Emmes Group, we’re shaping the future of clinical research—where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we’ve led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.Through our two business units—Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions —we are modernizing clinical trials and accelerating the development of life-changing therapies.We believe that every clinical breakthrough starts with people—people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.The Associate Site and Patient Access Strategist supports the pre-award proposal and bid defense process under the guidance of senior team members. The Associate Site and Patient Access Strategist assists in gathering and organizing data from relevant sources and analytics tools to help inform country, site, and patient strategy for clinical trials. The Associate also supports post-award feasibility activities, helping to compile and organize feasibility assessment data to contribute to a successful study endpoint.

Responsibilities

• In pre-award, supports development of country/site/patient solutions by gathering and organizing data, drafting proposal text, and assisting with bid defense preparation.
• Assists with protocol prediction by helping to compile patient profile and standard of care information
• Supports awarded feasibility offerings by helping to prepare site assessment surveys, organizing data received from sites, and assisting with tracking site tiering parameters.
• Translates feasibility assessment data/results into visual presentations and/or written reports, and supports delivery to internal/external stakeholders as directed.
• Performs other duties as assigned
• Complies with all policies and standards

Qualifications

• Bachelor's Degree in a life science, communication and or scientific discipline. Required
• 2-3 years Relevant clinical research/drug development experience, with exposure to feasibility, site identification/selection, study start-up, patient recruitment planning, or related clinical operations activities Required
• Excellent independent judgment and decision making skills. High
• Adept at analyzing data to form independent decisions. High
• Effective time management skills as demonstrated through management of multiple projects. High
• Excellent oral and written communication skills. High
• Proven ability to make difficult decisions under pressure, at times without all desired information. High
• Excellent interpersonal, problem solving and conflict resolution skills. High
• Good leadership skills including experience leading a global and cross functional team. High
• Strong understanding of budgeting and forecasting. High
• Strong computer skills. High

 

If you’re looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.CONNECT WITH US!Find us on LinkedIn:/the-emmes-group/Visit our website:https://www.theemmesgroup.com/