Oversee study start-up, site activation, and close-out activities while managing study plans and essential documents.
Collaborate with cross-functional teams, sponsors, and vendors to ensure timely and compliant project execution.
Mentor CTA team members and contribute to TMF quality, inspection readiness, and regulatory compliance.
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. They are a collaborative community committed to making a meaningful impact on global health, valuing team members and empowering them.
Process, review, and manage imaging data for assigned clinical trials to ensure accuracy and protocol compliance.
Communicate with internal study teams and clinical sites to resolve data-related issues and maintain accurate records.
Support departmental initiatives, prepare workflow documentation, and participate in continuous process improvement.
Clario is a leading provider of endpoint data solutions for the clinical trials industry, generating high-quality clinical evidence for life sciences companies. With over 30,000 trials supported in more than 100 countries and a global team of experts, Clario provides a collaborative, fast-paced environment committed to transforming lives through advanced clinical research.
Own Profound's patient engagement and recruitment strategy across sites, studies, and therapeutic areas.
Lead the team and build scalable approaches to patient identification, outreach, and retention.
Establish KPIs, reporting rhythms, and data-driven forecasts to optimize enrollment performance.
Profound Research partners with community physicians to offer clinical trials as a therapeutic option for patients, handling infrastructure and compliance so physicians focus on care. As a growing company, they values compassion, urgency, solution orientation, and excellence in a mission-driven, collaborative culture.
Lead and manage a team of Project Directors and Project Managers for global clinical trials.
Oversee project delivery, sponsor interactions, and profitability across clinical programs.
Ensure compliance with GCP/ICH and drive continuous improvement and KPIs.
Precision Medicine Group is a precision medicine company providing clinical research and development services. They emphasize quality, people, clients, and performance, with a collaborative team environment.
Lead the implementation and adoption of new technologies, systems, and business processes that support feasibility, patient engagement, and site solutions.
Collaborate with internal stakeholders, functional experts, technical teams, and external vendors to deliver successful technology implementations.
Develop, organize, and maintain training materials, process documentation, performance metrics, and proposal-ready capability resources.
Our partner is a clinical research organization that enables patient and site solutions through technology and process improvements. They offer a collaborative, inclusive, and globally connected work environment that supports professional growth and innovation.