Independently manages significant aspects of clinical trials and research projects.
Trains and provides guidance to less experienced staff, and oversees data management.
Ensures compliance with regulations, monitors IRB submissions, and interfaces with study sponsors.
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate and prepare leaders for the future. The university is committed to diversity and inclusion, providing a supportive environment for staff and faculty.
Develop and maintain successful working relationships with study sites, serving as the primary point of contact for clinical trial operations.
Conduct monitoring visits to ensure compliance with protocols, GCP, and regulatory requirements, preparing high-quality reports.
Collaborate with cross-functional teams including Clinical Project Managers, Data Management, and Regulatory Affairs to ensure end-to-end study execution.
CVRx pioneers unique therapies that harness and harmonize the body's natural systems, benefiting society and making CVRx a universal role model in healthcare. The company values commitments to others and fosters a culture of teamwork, collaboration, and positivity in a purpose-driven startup environment.
Serve as a senior clinical resource guiding complex clinical trials, research, and data-collection activities.
Recruit and collaborate with clinical investigators on study design, costs, timelines, and execution.
Oversee Phase III and Phase IV human clinical trials and ensure adherence to protocols and regulatory requirements.
This role is listed on behalf of a partner company that supports innovative, minimally invasive solutions in the vascular care space. They offer opportunities for professional growth within a global healthcare environment.
Conduct independent clinical research and interpret specialty society guidelines to originate automated payment integrity logic.
Author end-to-end logic from scratch, translating clinical documentation and coding frameworks into precise parameters.
Lead cross-functional policy development and own concept rollouts from discovery through post-launch tracking.
Devoted Health is a healthcare company on a mission to improve the health and well-being of older Americans by providing a seamless care platform. Founded in 2017, it fosters a culture of innovation and collaboration, with a focus on data and AI to deliver exceptional member experiences.
Take your career to the next level and lead challenging global clinical research projects.
Manage the full scope of responsibilities and get hands-on involvement in every aspect of the study.
Work remotely or hybrid while managing multi-functional project teams and client relationships.
PSI is a leading Contract Research Organization with 30 years of experience, offering a balance between stability and innovation. They focus on delivering quality and on-time services across various therapeutic indications, and invest in their people's professional development.
Manage global, multi-center clinical research projects in a variety of therapeutic areas.
Deliver projects on time, within budget, and in accordance with high quality standards.
Lead and mentor project teams, and serve as the primary point of contact to clients on all project matters.
PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. They focus on delivering quality and on-time services across a variety of therapeutic indications.
Conduct high-volume outbound outreach and respond to inbound patient inquiries for vaccine/flu clinical trials.
Pre-screen potential participants, schedule screening visits, and maintain accurate records across systems.
Support patient follow-up to improve engagement and reduce barriers to participation.
Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. They are a growing organization that values compassion, urgency, solution orientation, and excellence.
Serves as regulatory document specialist for clinical trial start-up, maintenance, and close-out.
Collects, reviews, and maintains essential documents in the electronic Trial Master File (eTMF).
Communicates with study teams and sites to ensure regulatory files remain complete and inspection-ready.
St. Jude Children’s Research Hospital is a leading research and treatment center focused on pediatric catastrophic diseases. It is a large institution with a collaborative culture and a strong emphasis on finding cures and saving children.
Negotiate and manage budgets and contracts for clinical research studies.
Develop country and site budgets and track negotiation progress.
Ensure compliance with financial procedures and ICH GCP guidelines.
Fortrea is a clinical research organization dedicated to streamlining clinical trials and ensuring compliance with global regulations. The company fosters a collaborative, family-oriented culture with a focus on teamwork and excellence.